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INSTITUT FÜR MEDIZINISCHE INFORMATIK, STATISTIK UND EPIDEMIOLOGIE Deutsche Website

Publications

2017


  • Tönjes A, Scholz M, Krüger J, Krause K, Schleinitz D, Kirsten H, Gebhardt C, Marzi C, Grallert H, Ladenvall C, Heyne H, Laurila E, Kriebel J, Meisinger C, Rathmann W, Gieger C, Groop L, Prokopenko I, Isomaa B, Beutner F, Kratzsch J, Fischer-Rosinsky A, Pfeiffer A, Krohn K, Spranger J, Thiery J, Blüher M, Stumvoll M, Kovacs P: Genome wide meta-analysis identifies novel determinants of circulating serum progranulin. Human molecular genetics 2017. (source)
  • Thiele AG, Gausche R, Lindenberg C, Beger C, Arelin M, Rohde C, Mütze U, Weigel JF, Mohnike K, Baerwald C, Scholz M, Kiess W, Pfäffle R, Beblo S: Growth and Final Height Among Children With Phenylketonuria. Pediatrics 2017, 140. (source)
  • Gross A, Tönjes A, Scholz M: On the impact of relatedness on SNP association analysis. BMC genetics 2017, 18:104. (source)
  • Schirm S, Engel C, Loibl S, Loeffler M, Scholz M: Model-based optimization of G-CSF treatment during cytotoxic chemotherapy. Journal of cancer research and clinical oncology 2017. (source)
  • Zeller T, Seiffert M, Müller C, Scholz M, Schäffer A, Ojeda F, Drexel H, Mündlein A, Kleber ME, März W, Sinning C, Brunner FJ, Waldeyer C, Keller T, Saely CH, Sydow K, Thiery J, Teupser D, Blankenberg S, Schnabel R: Genome-Wide Association Analysis for Severity of Coronary Artery Disease Using the Gensini Scoring System. Frontiers in cardiovascular medicine 2017, 4:57. (source)
  • Remmler J, Schneider C, Treuner-Kaueroff T, Bartels M, Seehofer D, Scholz M, Berg T, Kaiser T: Increased Level of Interleukin 6 Associates With Increased 90-day and 1-year Mortality in Patients With End-stage Liver Disease. Clinical gastroenterology and hepatology: the official clinical practice journal of the American Gastroenterological Association 2017. (source)
  • Oak P, Pritzke T, Thiel I, Koschlig M, Mous DS, Windhorst A, Jain N, Eickelberg O, Foerster K, Schulze A, Goepel W, Reicherzer T, Ehrhardt H, Rottier RJ, Ahnert P, Gortner L, Desai TJ, Hilgendorff A: Attenuated PDGF signaling drives alveolar and microvascular defects in neonatal chronic lung disease. EMBO molecular medicine 2017. (source)
  • Lukowski SW, Lloyd-Jones LR, Holloway A, Kirsten H, Hemani G, Yang J, Small K, Zhao J, Metspalu A, Dermitzakis ET, Gibson G, Spector TD, Thiery J, Scholz M, Montgomery GW, Esko T, Visscher PM, Powell JE: Genetic correlations reveal the shared genetic architecture of transcription in human peripheral blood. Nature communications 2017, 8:483. (source)
  • Buchmann N, Scholz M, Lill CM, Burkhardt R, Eckardt R, Norman K, Loeffler M, Bertram L, Thiery J, Steinhagen-Thiessen E, Demuth I: Association between lipoprotein(a) level and type 2 diabetes: no evidence for a causal role of lipoprotein(a) and insulin. Acta diabetologica 2017. (source)
  • Mayer T, Bolliger D, Scholz M, Reuthebuch O, Gregor M, Meier P, Grapow M, Seeberger MD, Fassl J: Urine Biomarkers of Tubular Renal Cell Damage for the Prediction of Acute Kidney Injury After Cardiac Surgery-A Pilot Study. Journal of cardiothoracic and vascular anesthesia 2017. (source)
  • Rosendahl J, Kirsten H, Hegyi E, Kovacs P, Weiss FU, Laumen H, Lichtner P, Ruffert C, Chen J, Masson E, Beer S, Zimmer C, Seltsam K, Algül H, Bühler F, Bruno MJ, Bugert P, Burkhardt R, Cavestro GM, Cichoz-Lach H, Farré A, Frank J, Gambaro G, Gimpfl S, Grallert H, Griesmann H, Grützmann R, Hellerbrand C, Hegyi P, Hollenbach M et al.: Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis. Gut 2017. (source)
  • Zewinger S, Kleber ME, Tragante V, McCubrey RO, Schmidt AF, Direk K, Laufs U, Werner C, Koenig W, Rothenbacher D, Mons U, Breitling LP, Brenner H, Jennings RT, Petrakis I, Triem S, Klug M, Filips A, Blankenberg S, Waldeyer C, Sinning C, Schnabel RB, Lackner KJ, Vlachopoulou E, Nygård O, Svingen GFT, Pedersen ER, Tell GS, Sinisalo J, Nieminen MS et al.: Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study. The lancet. Diabetes & endocrinology 2017. (source)
  • Kaiser T, Kinny-Koster B, Bartels M, Berg T, Scholz M, Engelmann C, Seehofer D, Becker S, Ceglarek U, Thiery J: Cholesterol esterification in plasma as a biomarker for liver function and prediction of mortality. BMC gastroenterology 2017, 17:57. (source)
  • Pott J, Burkhardt R, Beutner F, Horn K, Teren A, Kirsten H, Holdt LM, Schuler G, Teupser D, Loeffler M, Thiery J, Scholz M: Genome-wide meta-analysis identifies novel loci of plaque burden in carotid artery. Atherosclerosis 2017, 259:32-40. (source)
  • Glock F, Scholz M, Kuehnapfel A, Kiess W: Validity and reliability of three-dimensional scanning compared with conventional anthropometry for children and adolescents-response to the rebuttal by Sabour. Pediatric research 2017. (source)
  • Becker S, Kinny-Koster B, Bartels M, Scholz M, Seehofer D, Berg T, Engelmann C, Thiery J, Ceglarek U, Kaiser T: Low sphingosine-1-phosphate plasma levels are predictive for increased mortality in patients with liver cirrhosis. PloS one 2017, 12:e0174424. (source)
  • Teren A, Kirsten H, Beutner F, Scholz M, Holdt LM, Teupser D, Gutberlet M, Thiery J, Schuler G, Eitel I: Alteration of Multiple Leukocyte Gene Expression Networks is Linked with Magnetic Resonance Markers of Prognosis After Acute ST-Elevation Myocardial Infarction. Scientific reports 2017, 7:41705. (source)
  • Neef NE, Muller B, Liebig J, Schaadt G, Grigutsch M, Gunter TC, Wilcke A, Kirsten H, Skeide MA, Kraft I, Kraus N, Emmrich F, Brauer J, Boltze J, Friederici AD: Dyslexia risk gene relates to representation of sound in the auditory brainstem. Developmental cognitive neuroscience 2017, 24:63-71. (source)
  • Kuehnapfel A, Schwarzenberger F, Scholz M: On the Conditional Power in Survival Time Analysis Considering Cure Fractions. The international journal of biostatistics 2017. (source)
  • Kuehnapfel A, Ahnert P, Loeffler M, Scholz M: Body surface assessment with 3D laser-based anthropometry: reliability, validation, and improvement of empirical surface formulae. European journal of applied physiology 2017. (source)
  • Glock F, Vogel M, Naumann S, Kuehnapfel A, Scholz M, Hiemisch A, Kirsten T, Rieger K, Koerner A, Loeffler M, Kiess W: Validity and intra-observer reliability of three-dimensional scanning compared to conventional anthropometry for children and adolescents from a population-based cohort study. Pediatric research 2017. (source)
  • 2016


  • Kraft I, Schreiber J, Cafiero R, Metere R, Schaadt G, Brauer J, Neef NE, Müller B, Kirsten H, Wilcke A, Boltze J, Friederici AD, Skeide MA: Predicting early signs of dyslexia at a preliterate age by combining behavioral assessment with structural MRI. NeuroImage 2016, 143:378-386. (source)
  • Treudler R, Walther F, Ahnert P, Simon J: Unerwunschte Arzneimittelreaktionen beim älteren Menschen. Erste Daten aus dem Leipziger Forschungszentrum für Zivilisationserkrankungen (LIFE). Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete. (source)
  • Roshyara NR, Horn K, Kirsten H, Ahnert P, Scholz M: Comparing performance of modern genotype imputation methods in different ethnicities. Scientific reports 2016, 6:34386. (source)
  • Loley C, Alver M, Assimes TL, Bjonnes A, Goel A, Gustafsson S, Hernesniemi J, Hopewell JC, Kanoni S, Kleber ME, Lau KW, Lu Y, Lyytikainen L, Nelson CP, Nikpay M, Qu L, Salfati E, Scholz M, Tukiainen T, Willenborg C, Won H, Zeng L, Zhang W, Anand SS, Beutner F, Bottinger EP, Clarke R, Dedoussis G, Do R, Esko T et al.: No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis. Scientific reports 2016, 6:35278. (source)
  • Vausort M, Salgado-Somoza A, Zhang L, Leszek P, Scholz M, Teren A, Burkhardt R, Thiery J, Wagner DR, Devaux Y: Myocardial Infarction-Associated Circular RNA Predicting Left Ventricular Dysfunction. Journal of the American College of Cardiology 2016, 68:1247-1248. (source)
  • Scherag A, Schoneweck F, Kesselmeier M, Taudien S, Platzer M, Felder M, Sponholz C, Rautanen A, Hill AVS, Hinds CJ, Hossain H, Suttorp N, Kurzai O, Slevogt H, Giamarellos-Bourboulis EJ, Armaganidis A, Trips E, Scholz M, Brunkhorst FM: Genetic Factors of the Disease Course after Sepsis: A Genome-Wide Study for 28Day Mortality. EBioMedicine 2016. (source)
  • Landgraf K, Scholz M, Kovacs P, Kiess W, Korner A: FTO Obesity Risk Variants Are Linked to Adipocyte IRX3 Expression and BMI of Children - Relevance of FTO Variants to Defend Body Weight in Lean Children? PloS one 2016, 11:e0161739. (source)
  • Holdt LM, Stahringer A, Sass K, Pichler G, Kulak NA, Wilfert W, Kohlmaier A, Herbst A, Northoff BH, Nicolaou A, Gabel G, Beutner F, Scholz M, Thiery J, Musunuru K, Krohn K, Mann M, Teupser D: Circular non-coding RNA ANRIL modulates ribosomal RNA maturation and atherosclerosis in humans. Nature communications 2016, 7:12429. (source)
  • Hasenclever D, Scholz M: Comparing Measures of Association in 2×2 Probability Tables. The Open Statistics 2016, 7:20-35. (source)
  • Skeide MA, Kraft I, Muller B, Schaadt G, Neef NE, Brauer J, Wilcke A, Kirsten H, Boltze J, Friederici AD: NRSN1 associated grey matter volume of the visual word form area reveals dyslexia before school. Brain: a journal of neurology 2016. (source)
  • Rösch K, Scholz M, Hasenclever D: Modeling combined chemo- and immunotherapy of high-grade non-Hodgkin lymphoma. Leukemia & lymphoma 2016, 57:1697-1708. (source)
  • Löffler-Wirth H, Willscher E, Ahnert P, Wirkner K, Engel C, Loeffler M, Binder H: Novel Anthropometry Based on 3D-Bodyscans Applied to a Large Population Based Cohort. PloS one 2016, 11:e0159887. (source)
  • Kinny-Koster B, Bartels M, Becker S, Scholz M, Thiery J, Ceglarek U, Kaiser T: Plasma Amino Acid Concentrations Predict Mortality in Patients with End-Stage Liver Disease. PloS one 2016, 11:e0159205. (source)
  • Freiermuth D, Mets B, Bolliger D, Reuthebuch O, Doebele T, Scholz M, Gregor M, Haschke M, Seeberger MD, Fassl J: Sevoflurane and Isoflurane-Pharmacokinetics, Hemodynamic Stability, and Cardioprotective Effects During Cardiopulmonary Bypass. Journal of cardiothoracic and vascular anesthesia 2016. (source)
  • Ahnert P, Creutz P, Scholz M, Schutte H, Engel C, Hossain H, Chakraborty T, Bauer M, Kiehntopf M, Volker U, Hammerschmidt S, Loeffler M, Suttorp N: PROGRESS - prospective observational study on hospitalized community acquired pneumonia. BMC pulmonary medicine 2016, 16:108. (source)
  • Muller B, Wilcke A, Czepezauer I, Ahnert P, Boltze J, Kirsten H: Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort. Scientific reports 2016, 6:27901. (source)
  • Schirm S, Ahnert P, Wienhold S, Mueller-Redetzky H, Nouailles-Kursar G, Loeffler M, Witzenrath M, Scholz M: A Biomathematical Model of Pneumococcal Lung Infection and Antibiotic Treatment in Mice. PloS one 2016, 11:e0156047. (source)
  • Kuehnapfel A, Ahnert P, Loeffler M, Broda A, Scholz M: Reliability of 3D laser-based anthropometry and comparison with classical anthropometry. Scientific reports 2016, 6:26672. (source)
  • Jawinski P, Tegelkamp S, Sander C, Hantzsch M, Huang J, Mauche N, Scholz M, Spada J, Ulke C, Burkhardt R, Reif A, Hegerl U, Hensch T: Time to wake up: No impact of COMT Val158Met gene variation on circadian preferences, arousal regulation and sleep. Chronobiology international 2016,:1-13. (source)
  • Spada J, Scholz M, Kirsten H, Hensch T, Horn K, Jawinski P, Ulke C, Burkhardt R, Wirkner K, Loeffler M, Hegerl U, Sander C: Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study. Journal of sleep research 2016. (source)
  • Teren A, Beutner F, Wirkner K, Löffler M, Scholz M: Relationship Between Determinants of Arterial Stiffness Assessed by Diastolic and Suprasystolic Pulse Oscillometry: Comparison of Vicorder and Vascular Explorer. Medicine 2016, 95:e2963. (source)
  • Wilcke A, Müller B, Schaadt G, Kirsten H, Boltze J: High acceptance of an early dyslexia screening test involving genetic analyses in Germany. European journal of human genetics: EJHG 2016, 24:178-182. (source)
  • Weissgerber A, Scholz M, Teren A, Sandri M, Teupser D, Gielen S, Thiery J, Schuler G, Beutner F: The value of noncoronary atherosclerosis for identifying coronary artery disease: results of the Leipzig LIFE Heart Study. Clinical research in cardiology: official journal of the German Cardiac Society 2016, 105:172-181. (source)
  • Peschka A, Berger T, Maier T, Scholz M, Lüth TC, Strauß G: Evaluation eines Mikromanipulators für die Mittelohrchirurgie: Eine präklinische Studie. Laryngo- rhino- otologie 2016, 95:112-117. (source)
  • Müller B, Wilcke A, Boulesteix A, Brauer J, Passarge E, Boltze J, Kirsten H: Improved prediction of complex diseases by common genetic markers: state of the art and further perspectives. Human genetics 2016, 135:259-272. (source)
  • Ebert T, Kralisch S, Wurst U, Scholz M, Stumvoll M, Kovacs P, Fasshauer M, Tönjes A: Association of metabolic parameters and rs726344 in FNDC5 with serum irisin concentrations. International journal of obesity 2016, 40:260-265. (source)
  • Kirsten H, Scholz M, Kovacs P, Grallert H, Peters A, Strauch K, Frank J, Rietschel M, Nöthen MM, Witt H, Rosendahl J: Genetic variants of lipase activity in chronic pancreatitis. Gut 2016, 65:184-185. (source)
  • 2015


  • Waseem Z, Lindner J, Sgouropoulou S, Eibel S, Probst S, Scholz M, Ender J: Independent Risk Factors for Fast-Track Failure Using a Predefined Fast-Track Protocol in Preselected Cardiac Surgery Patients. Journal of cardiothoracic and vascular anesthesia 2015, 29:1461-1465. (source)
  • Jawinski P, Sander C, Mauche N, Spada J, Huang J, Schmidt A, Häntzsch M, Burkhardt R, Scholz M, Hegerl U, Hensch T: Brain Arousal Regulation in Carriers of Bipolar Disorder Risk Alleles. Neuropsychobiology 2015, 72:65-73. (source)
  • Skeide MA, Kirsten H, Kraft I, Schaadt G, Müller B, Neef N, Brauer J, Wilcke A, Emmrich F, Boltze J, Friederici AD: Genetic dyslexia risk variant is related to neural connectivity patterns underlying phonological awareness in children. NeuroImage 2015, 118:414-421. (source)
  • CARDIoGRAMplusC4D Consortium: A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Nature genetics 2015, 47:1121-1130. (source)
  • Burkhardt R, Kirsten H, Beutner F, Holdt LM, Gross A, Teren A, Tönjes A, Becker S, Krohn K, Kovacs P, Stumvoll M, Teupser D, Thiery J, Ceglarek U, Scholz M: Integration of Genome-Wide SNP Data and Gene-Expression Profiles Reveals Six Novel Loci and Regulatory Mechanisms for Amino Acids and Acylcarnitines in Whole Blood. PLOS Genet. 2015, 11:e1005510. (source)
  • Breitling C, Gross A, Büttner P, Weise S, Schleinitz D, Kiess W, Scholz M, Kovacs P, Körner A: Genetic Contribution of Variants near SORT1 and APOE on LDL Cholesterol Independent of Obesity in Children. PLOS ONE 2015, 10:e0138064. (source)
  • Ronke C, Dannemann M, Halbwax M, Fischer A, Helmschrodt C, Brügel M, André C, Atencia R, Mugisha L, Scholz M, Ceglarek U, Thiery J, Pääbo S, Prüfer K, Kelso J: Lineage-Specific Changes in Biomarkers in Great Apes and Humans. PLOS ONE 2015, 10:e0134548. (source)
  • Roshyara NR, Scholz M: Impact of genetic similarity on imputation accuracy. BMC Genet. 2015, 16:90. (source)
  • Männel C, Meyer L, Wilcke A, Boltze J, Kirsten H, Friederici AD: Working-memory endophenotype and dyslexia-associated genetic variant predict dyslexia phenotype. Cortex 2015, 71:291-305. (source)
  • Loeffler M, Engel C, Ahnert P, Alfermann D, Arelin K, Baber R, Beutner F, Binder H, Brähler E, Burkhardt R, Ceglarek U, Enzenbach C, Fuchs M, Glaesmer H, Girlich F, Hagendorff A, Häntzsch M, Hegerl U, Henger S, Hensch T, Hinz A, Holzendorf V, Husser D, Kersting A, Kiel A, Kirsten T, Kratzsch J, Krohn K, Luck T, Melzer S et al.: The LIFE-Adult-Study: objectives and design of a population-based cohort study with 10,000 deeply phenotyped adults in Germany. BMC public health 2015, 15:691. (source)
  • Wichmann G, Rosolowski M, Krohn K, Kreuz M, Boehm A, Reiche A, Scharrer U, Halama D, Bertolini J, Bauer U, Holzinger D, Pawlita M, Hess J, Engel C, Hasenclever D, Scholz M, Ahnert P, Kirsten H, Hemprich A, Wittekind C, Herbarth O, Horn F, Dietz A, Loeffler M: The role of HPV RNA transcription, immune response-related gene expression and disruptive TP53 mutations in diagnostic and prognostic profiling of head and neck cancer. International journal of cancer. Journal international du cancer 2015, 137:2846-2857. (source)
  • Nitzsche B, Frey S, Collins LD, Seeger J, Lobsien D, Dreyer A, Kirsten H, Stoffel MH, Fonov VS, Boltze J: A stereotaxic, population-averaged T1w ovine brain atlas including cerebral morphology and tissue volumes. Frontiers in neuroanatomy 2015, 9:69. (source)
  • Kirsten H, Al-Hasani H, Holdt L, Gross A, Beutner F, Krohn K, Horn K, Ahnert P, Burkhardt R, Reiche K, Hackermüller J, Löffler M, Teupser D, Thiery J, Scholz M: Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†. Human molecular genetics 2015, 24:4746-4763. (source)
  • Hass J, Walton E, Wright C, Beyer A, Scholz M, Turner J, Liu J, Smolka MN, Roessner V, Sponheim SR, Gollub RL, Calhoun VD, Ehrlich S: Associations between DNA methylation and schizophrenia-related intermediate phenotypes - a gene set enrichment analysis. Progress in neuro-psychopharmacology & biological psychiatry 2015, 59:31-39. (source)
  • Boehm A, Lindner F, Wichmann G, Bauer U, Wittekind C, Knoedler M, Lordick F, Dietzsch S, Scholz M, Kortmann R, Dietz A, Wittekind C, Dietz A, Scholz M: Impact of indication-shift of primary and adjuvant chemo radiation in advanced laryngeal and hypopharyngeal squamous cell carcinoma. Eur Arch Otorhinolaryngol 2015, 272:2017-2025. (source)
  • Schöneweck F, Kuhnt E, Scholz M, Brunkhorst FM, Scherag A: Common genomic variation in the FER gene: useful to stratify patients with sepsis due to pneumonia? Intensive care medicine 2015, 41:1379-1381. (source)
  • Mathias D, Mitchel, Ronald E J, Barclay M, Wyatt H, Bugden M, Priest ND, Whitman SC, Scholz M, Hildebrandt G, Kamprad M, Glasow A, Mitchel REJ: Low-Dose Irradiation Affects Expression of Inflammatory Markers in the Heart of ApoE -/- Mice. PLOS ONE 2015, 10:e0119661. (source)
  • Liu X, Hinney A, Scholz M, Scherag A, Tönjes A, Stumvoll M, Stadler PF, Hebebrand J, Böttcher Y: Indications for potential parent-of-origin effects within the FTO gene. PLOS ONE 2015, 10:e0119206. (source)
  • Fjeld K, Weiss FU, Lasher D, Rosendahl J, Chen J, Johansson BB, Kirsten H, Ruffert C, Masson E, Steine SJ, Bugert P, Cnop M, Grützmann R, Mayerle J, Mössner J, Ringdal M, Schulz H, Sendler M, Simon P, Sztromwasser P, Torsvik J, Scholz M, Tjora E, Férec C, Witt H, Lerch MM, Njølstad PR, Johansson S, Molven A: A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis. Nature genetics 2015, 47:518-522. (source)
  • Xu L, Holland H, Kirsten H, Ahnert P, Krupp W, Bauer M, Schober R, Mueller W, Fritzsch D, Meixensberger J, Koschny R: Three gangliogliomas: Results of GTG-banding, SKY, genome-wide high resolution SNP-array, gene expression and review of the literature. Neuropathology: official journal of the Japanese Society of Neuropathology 2015, 35:148-157. (source)
  • Kraft I, Cafiero R, Schaadt G, Brauer J, Neef NE, Muller B, Kirsten H, Wilcke A, Boltze J, Friederici AD, Skeide MA: Cortical differences in preliterate children at familiar risk of dyslexia are similar to those observed in dyslexic readers. Brain: a journal of neurology 2015, 138:e378. (source)
  • Hass J, Walton E, Kirsten H, Turner J, Wolthusen R, Roessner V, Sponheim SR, Holt D, Gollub R, Calhoun VD, Ehrlich S: Complexin2 modulates working memory-related neural activity in patients with schizophrenia. European archives of psychiatry and clinical neuroscience 2015, 265:137-145. (source)
  • Derikx MH, Kovacs P, Scholz M, Masson E, Chen J, Ruffert C, Lichtner P, Te Morsche, Rene H M, Cavestro GM, Algül H, Berg T, Bödeker H, Blüher M, Bruno MJ, Buch S, Bugert P, Cichoz-Lach H, Dabrowski A, Farré A, Frank J, Gasiorowska A, Geisz A, Goni E, Grothaus J, Grützmann R, Haas S, Hampe J, Hellerbrand C, Hegyi P, Huster D et al.: Polymorphisms at PRSS1-PRSS2 and CLDN2-MORC4 loci associate with alcoholic and non-alcoholic chronic pancreatitis in a European replication study. Gut 2015, 64:1426-1433. (source)
  • Berger T, Kaiser T, Scholz M, Bachmann A, Ceglarek U, Hesse G, Hagemeyer B, Stumvoll M, Thiery J, Dietz A: Fibrinogen is not a prognostic factor for response to HELP-apheresis in sudden sensorineural hearing loss (SSHL). European archives of oto-rhino-laryngology: official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS): affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2015, 272:3693-3703. (source)
  • Köberle M, Müller K, Kamprad M, Horn F, Scholz M: Monitoring Disease Progression and Therapeutic Response in a Disseminated Tumor Model for Non-Hodgkin Lymphoma by Bioluminescence Imaging. Molecular imaging 2015, 14:400-413. (source)
  • 2014


  • Tönjes A, Scholz M, Breitfeld J, Marzi C, Grallert H, Gross A, Ladenvall C, Schleinitz D, Krause K, Kirsten H, Laurila E, Kriebel J, Thorand B, Rathmann W, Groop L, Prokopenko I, Isomaa B, Beutner F, Kratzsch J, Thiery J, Fasshauer M, Klöting N, Gieger C, Blüher M, Stumvoll M, Kovacs P: Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerin. PLOS Genet. 2014, 10:e1004854. (source)
  • Schirm S, Engel C, Loeffler M, Scholz M: Modelling chemotherapy effects on granulopoiesis. BMC Syst Biol 2014, 8:138. (source)
  • Walton E, Liu J, Hass J, White T, Scholz M, Roessner V, Gollub R, Calhoun VD, Ehrlich S: MB-COMT promoter DNA methylation is associated with working-memory processing in schizophrenia patients and healthy controls. Epigenetics: official journal of the DNA Methylation Society 2014, 9:1101-1107. (source)
  • Roshyara NR, Kirsten H, Horn K, Ahnert P, Scholz M: Impact of pre-imputation SNP-filtering on genotype imputation results. BMC Genet. 2014, 15:88. (source)
  • Probst S, Cech C, Haentschel D, Scholz M, Ender J: A specialized post anaesthetic care unit improves fast-track management in cardiac surgery: a prospective randomized trial. Crit Care 2014, 18:468. (source)
  • Burkhardt J, Blume M, Petit-Teixeira E, Hugo Teixeira V, Steiner A, Quente E, Wolfram G, Scholz M, Pierlot C, Migliorini P, Bombardieri S, Balsa A, Westhovens R, Barrera P, Radstake, Timothy R D J, Alves H, Bardin T, Prum B, Emmrich F, Cornelis F, Ahnert P, Kirsten H: Cellular Adhesion Gene SELP Is Associated with Rheumatoid Arthritis and Displays Differential Allelic Expression // Cellular adhesion gene SELP is associated with rheumatoid arthritis and displays differential allelic expression. PLOS ONE 2014, 9:e103872. (source)
  • Roshyara NR, Scholz M: fcGENE: a versatile tool for processing and transforming SNP datasets. PLOS ONE 2014, 9:e97589. (source)
  • Gross A, Schirm S, Scholz M: Ycasd - a tool for capturing and scaling data from graphical representations. BMC Bioinformatics 2014, 15:219. (source)
  • Flehmig G, Scholz M, Klöting N, Fasshauer M, Tönjes A, Stumvoll M, Youn B, Blüher M, Moro C: Identification of adipokine clusters related to parameters of fat mass, insulin sensitivity and inflammation. PLOS ONE 2014, 9:e99785. (source)
  • Schirm S, Engel C, Loeffler M, Scholz M: A combined model of human erythropoiesis and granulopoiesis under growth factor and chemotherapy treatment. Theor Biol Med Model 2014, 11:24. (source)
  • Mueller B, Ahnert P, Burkhardt J, Brauer J, Czepezauer I, Quente E, Boltze J, Wilcke A, Kirsten H: Genetic risk variants for dyslexia on chromosome 18 in a German cohort. Genes Brain Behav. 2014, 13:350-356. (source)
  • Hackermüller J, Reiche K, Otto C, Hösler N, Blumert C, Brocke-Heidrich K, Böhlig L, Nitsche A, Kasack K, Ahnert P, Krupp W, Engeland K, Stadler PF, Horn F: Cell cycle, oncogenic and tumor suppressor pathways regulate numerous long and macro non-protein-coding RNAs. Genome Biol. 2014, 15:R48. (source)
  • Roesch K, Hasenclever D, Scholz M: Modelling lymphoma therapy and outcome. Bulletin of mathematical biology 2014, 76:401-430. (source)
  • Eszlinger M, Krogdahl A, Münz S, Rehfeld C, Precht Jensen, Eva Magrethe, Ferraz C, Bösenberg E, Drieschner N, Scholz M, Hegedüs L, Paschke R: Impact of molecular screening for point mutations and rearrangements in routine air-dried fine-needle aspiration samples of thyroid nodules. Thyroid 2014, 24:305-313. (source)
  • Spada J, Sander C, Burkhardt R, Häntzsch M, Mergl R, Scholz M, Hegerl U, Hensch T: Genetic association of objective sleep phenotypes with a functional polymorphism in the neuropeptide S receptor gene. PLOS ONE 2014, 9:e98789. (source)
  • 2013


  • Zeynalova S, Ziepert M, Scholz M, Schirm S, Zwick C, Pfreundschuh M, Loeffler M: Comparison and modelling of pegylated or unpegylated G-CSF schedules in CHOP-14 regimen of elderly patients with aggressive B-cell lymphoma. Ann. Hematol. 2013, 92:1641-1652. (source)
  • Wienhold R, Scholz M, Adler J, Günster C, Paschke R: The management of thyroid nodules: a retrospective analysis of health insurance data. Dtsch Arztebl Int 2013, 110:827-834. (source)
  • Krinner A, Roeder I, Loeffler M, Scholz M: Merging concepts - coupling an agent-based model of hematopoietic stem cells with an ODE model of granulopoiesis. BMC Syst Biol 2013, 7:117. (source)
  • Holmes MV, Simon T, Exeter HJ, Folkersen L, Asselbergs FW, Guardiola M, Cooper JA, Palmen J, Hubacek JA, Carruthers KF, Horne BD, Brunisholz KD, Mega JL, van Iperen, Erik P A, Li M, Leusink M, Trompet S, Verschuren, Jeffrey J W, Hovingh GK, Dehghan A, Nelson CP, Kotti S, Danchin N, Scholz M, Haase CL, Rothenbacher D, Swerdlow DI, Kuchenbaecker KB, Staines-Urias E, Goel A et al.: Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study. J. Am. Coll. Cardiol. 2013, 62:1966-1976. (source)
  • Breitfeld J, Heiker JT, Böttcher Y, Schleinitz D, Tönjes A, Weidle K, Krause K, Kuettner EB, Scholz M, Kiess W, Sträter N, Beck-Sickinger AG, Stumvoll M, Körner A, Blüher M, Kovacs P: Analysis of a rare functional truncating mutation rs61757459 in vaspin (SERPINA12) on circulating vaspin levels. J. Mol. Med. 2013, 91:1285-1292. (source)
  • Teren A, Beutner F, Wirkner K, Loeffler M, Scholz M: Validity, intra- and inter-observer reliability of automated devices for the assessment of ankle brachial index using photo-plethysmography. BMC Cardiovasc Disord 2013, 13:81. (source)
  • Rehak M, Spies E, Scholz M, Wiedemann P: Behandlung der Patienten mit einem Venenastverschluss in Abhängigkeit von der Verschlussdauer. Ophthalmologe 2013, 110:966-974. (source)
  • Penk A, Förster Y, Scheidt HA, Nimptsch A, Hacker MC, Schulz-Siegmund M, Ahnert P, Schiller J, Rammelt S, Huster D: The pore size of PLGA bone implants determines the de novo formation of bone tissue in tibial head defects in rats. Magn Reson Med 2013, 70:925-935. (source)
  • Holland H, Xu L, Ahnert P, Kirsten H, Koschny R, Bauer M, Schober R, Meixensberger J, Krupp W: Comprehensive high-resolution genomic profiling and cytogenetics of two pediatric and one adult medulloblastoma. Pathol. Res. Pract. 2013, 209:541-547. (source)
  • Gast M, Tönjes A, Keller M, Horstmann A, Steinle N, Scholz M, Müller I, Villringer A, Stumvoll M, Kovacs P, Böttcher Y: The role of rs2237781 within GRM8 in eating behavior. Brain Behav 2013, 3:495-502. (source)
  • Holdt LM, Hoffmann S, Sass K, Langenberger D, Scholz M, Krohn K, Finstermeier K, Stahringer A, Wilfert W, Beutner F, Gielen S, Schuler G, Gäbel G, Bergert H, Bechmann I, Stadler PF, Thiery J, Teupser D: Alu elements in ANRIL non-coding RNA at chromosome 9p21 modulate atherogenic cell functions through trans-regulation of gene networks. PLOS Genet. 2013, 9:e1003588. (source)
  • Barkholt L, Flory E, Jekerle V, Lucas-Samuel S, Ahnert P, Bisset L, Büscher D, Fibbe W, Foussat A, Kwa M, Lantz O, Mačiulaitis R, Palomäki T, Schneider CK, Sensebé L, Tachdjian G, Tarte K, Tosca L, Salmikangas P: Risk of tumorigenicity in mesenchymal stromal cell-based therapies--bridging scientific observations and regulatory viewpoints. Cytotherapy 2013, 15:753-759. (source)
  • Aust G, Kerner C, Gonsior S, Sittig D, Schneider H, Buske P, Scholz M, Dietrich N, Oldenburg S, Karpus ON, Galle J, Amasheh S, Hamann J: Mice overexpressing CD97 in intestinal epithelial cells provide a unique model for mammalian postnatal intestinal cylindrical growth. Mol. Biol. Cell 2013, 24:2256-2268. (source)
  • Schirm S, Engel C, Loeffler M, Scholz M: A biomathematical model of human erythropoiesis under erythropoietin and chemotherapy administration. PLOS ONE 2013, 8:e65630. (source)
  • Hass J, Walton E, Kirsten H, Liu J, Priebe L, Wolf C, Karbalai N, Gollub R, White T, Roessner V, Müller KU, Paus T, Smolka MN, Schumann G, Scholz M, Cichon S, Calhoun VD, Ehrlich S: A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. PLOS ONE 2013, 8:e64872. (source)
  • Müller MK, Ludewig E, Oechtering G, Scholz M, Flegel T: The vacuum phenomenon in intervertebral disc disease of dogs based on computed tomography images. J Small Anim Pract 2013, 54:253-257. (source)
  • Thomas S, Kratzsch D, Schaab M, Scholz M, Grunewald S, Thiery J, Paasch U, Kratzsch J: Seminal plasma adipokine levels are correlated with functional characteristics of spermatozoa. Fertil. Steril. 2013, 99:1256-1263.e3. (source)
  • Hasenclever D, Scholz M: Comparing measures of association in 2x2 probability tables. arXiv:1302.6161v1 2013. (source)
  • 2012


  • Burkhardt J, Kirsten H, Holland H, Krupp W, Ligges C, Quente E, Boltze J, Ahnert P, Wilcke A: Association of rs2069459 in the CDK5 gene with dyslexia in a German cohort. Psychiatr. Genet. 2012, 22:307-308. (source)
  • Scholz M: Biomathematische Modellierung von Therapiewirkungen bei Lymphomerkrankungen - Ein Beitrag zur Medizinischen Systembiologie. Habilitation. Universität Leipzig (kein Review) 2012. (source)
  • Beutner F, Teren A, Gielen S, Schuler G, Wirkner K, Tiller D, Loeffler M, Scholz M: Automated photoplethysmography-based determination of ankle-brachial index: a validation study against Doppler sonography. Clin Res Cardiol 2012, 101:875-883. (source)
  • Ender A, Eibel S, Hasheminejad E, Scholz M, Kaisers UX, Mukherjee C, Ender J: \"Real-time-3-dimensional-full-volume\"-datensatz. Nutzen in der problemfokussierten intraoperativen transösophagealen echokardiographie. Anaesthesist 2012, 61:875-882. (source)
  • Wagner D, Bojko M, Peters M, Lorenz M, Voigt C, Kaminski A, Hasenclever D, Scholz M, Kranz A, Weise G, Boltze J: Impact of age on the efficacy of bone marrow mononuclear cell transplantation in experimental stroke. Exp Transl Stroke Med 2012, 4:17. (source)
  • Kirsten H, Wilcke A, Ligges C, Boltze J, Ahnert P: Association study of a functional genetic variant in KIAA0319 in German dyslexics. Psychiatr. Genet. 2012, 22:216-217. (source)
  • Scholz M, Schirm S, Wetzler M, Engel C, Loeffler M: Pharmacokinetic and -dynamic modelling of G-CSF derivatives in humans. Theor Biol Med Model 2012, 9:32. (source)
  • Burkhardt J, Kirsten H, Wolfram G, Quente E, Ahnert P: Differential allelic expression of IL13 and CSF2 genes associated with asthma. Genet. Mol. Biol. 2012, 35:567-574. (source)
  • Holland H, Ahnert P, Koschny R, Kirsten H, Bauer M, Schober R, Meixensberger J, Fritzsch D, Krupp W: Detection of novel genomic aberrations in anaplastic astrocytomas by GTG-banding, SKY, locus-specific FISH, and high density SNP-array. Pathol. Res. Pract. 2012, 208:325-330. (source)
  • Gross A, Ziepert M, Scholz M: KMWin--a convenient tool for graphical presentation of results from Kaplan-Meier survival time analysis. PLOS ONE 2012, 7:e38960. (source)
  • Fischer J, Böhm S, Scholz M, Müller T, Witt H, George J, Sarrazin C, Susser S, Schott E, Suppiah V, Booth DR, Stewart GJ, van Bömmel F, Brodzinski A, Fülöp B, Migaud P, Berg T: Combined effects of different interleukin-28B gene variants on the outcome of dual combination therapy in chronic hepatitis C virus type 1 infection. Hepatology 2012, 55:1700-1710. (source)
  • Glauche I, Horn K, Horn M, Thielecke L, Essers, M A G, Trumpp A, Roeder I: Therapy of chronic myeloid leukaemia can benefit from the activation of stem cells: simulation studies of different treatment combinations. Br. J. Cancer 2012, 106:1742-1752. (source)
  • Mukherjee C, Koch E, Banusch J, Scholz M, Kaisers UX, Ender J: Intrathecal morphine is superior to intravenous PCA in patients undergoing minimally invasive cardiac surgery. Ann Card Anaesth 2012, 15:122-127. (source)
  • Mukherjee C, Groeger S, Hogan M, Scholz M, Kaisers UX, Ender J: Pre-operative Tei Index does not predict left ventricular function immediately after mitral valve repair. Ann Card Anaesth 2012, 15:111-117. (source)
  • Wilcke A, Ligges C, Burkhardt J, Alexander M, Wolf C, Quente E, Ahnert P, Hoffmann P, Becker A, Müller-Myhsok B, Cichon S, Boltze J, Kirsten H: Imaging genetics of FOXP2 in dyslexia. Eur. J. Hum. Genet. 2012, 20:224-229. (source)
  • Maier T, Strauss G, Scholz M, Berger T, Kielhorn A, Entsfellner K, Willim C, Buscher W, Dietz A, Lueth TC: A new evaluation and training system for micro-telemanipulation at the middle ear. Conf Proc IEEE Eng Med Biol Soc 2012, 2012:932-935. (source)
  • 2011


  • Beutner F, Teupser D, Gielen S, Holdt LM, Scholz M, Boudriot E, Schuler G, Thiery J, Federici M: Rationale and design of the Leipzig (LIFE) Heart Study: phenotyping and cardiovascular characteristics of patients with coronary artery disease. PLOS ONE 2011, 6:e29070. (source)
  • Scholz M, Kirsten H: Comparison of scoring methods for the detection of causal genes with or without rare variants. BMC Proc 2011, 5 Suppl 9:S49. (source)
  • Holland H, Mocker K, Ahnert P, Kirsten H, Hantmann H, Koschny R, Bauer M, Schober R, Scholz M, Meixensberger J, Krupp W: High resolution genomic profiling and classical cytogenetics in a group of benign and atypical meningiomas. Cancer Genet 2011, 204:541-549. (source)
  • Veeramah KR, Tönjes A, Kovacs P, Gross A, Wegmann D, Geary P, Gasperikova D, Klimes I, Scholz M, Novembre J, Stumvoll M: Genetic variation in the Sorbs of eastern Germany in the context of broader European genetic diversity. Eur. J. Hum. Genet. 2011, 19:995-1001. (source)
  • Müller A, Scholz M, Blankenstein O, Binder G, Pfäffle R, Körner A, Kiess W, Heider A, Bidlingmaier M, Thiery J, Kratzsch J: Harmonization of growth hormone measurements with different immunoassays by data adjustment. Clin. Chem. Lab. Med. 2011, 49:1135-1142. (source)
  • Gross A, Tönjes A, Kovacs P, Veeramah KR, Ahnert P, Roshyara NR, Gieger C, Rueckert I, Loeffler M, Stoneking M, Wichmann H, Novembre J, Stumvoll M, Scholz M: Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays. BMC Genet. 2011, 12:67. (source)
  • Grey D, Sack U, Scholz M, Knaack H, Fricke S, Oppel C, Luderer D, Fangmann J, Emmrich F, Kamprad M: Increased CD64 expression on polymorphonuclear neutrophils indicates infectious complications following solid organ transplantation. Cytometry A 2011, 79:446-460. (source)
  • Aust G, Uptaite-Patapoviene M, Scholz M, Richter O, Rohm S, Blüher M: Circulating Nampt and RBP4 levels in patients with carotid stenosis undergoing carotid endarterectomy (CEA). Clin. Chim. Acta 2011, 412:1195-1200. (source)
  • Holland H, Livrea M, Ahnert P, Koschny R, Kirsten H, Meixensberger J, Bauer M, Schober R, Fritzsch D, Krupp W: Intracranial hemangiopericytoma: Case study with cytogenetics and genome wide SNP-A analysis. Pathol. Res. Pract. 2011, 207:310-316. (source)
  • Scholz M, Engert A, Franklin J, Josting A, Diehl V, Hasenclever D, Loeffler M: Impact of first- and second-line treatment for Hodgkin's lymphoma on the incidence of AML/MDS and NHL--experience of the German Hodgkin's Lymphoma Study Group analyzed by a parametric model of carcinogenesis. Ann. Oncol. 2011, 22:681-688. (source)
  • Lange T, Hubmann M, Burkhardt R, Franke G, Cross M, Scholz M, Leiblein S, Al-Ali HK, Edelmann J, Thiery J, Niederwieser D: Monitoring of WT1 expression in PB and CD34(+) donor chimerism of BM predicts early relapse in AML and MDS patients after hematopoietic cell transplantation with reduced-intensity conditioning. Leukemia 2011, 25:498-505. (source)
  • Jahns J, Anderegg U, Saalbach A, Rosin B, Patties I, Glasow A, Kamprad M, Scholz M, Hildebrandt G: Influence of low dose irradiation on differentiation, maturation and T-cell activation of human dendritic cells. Mutat. Res. 2011, 709-710:32-39. (source)
  • Mocker K, Holland H, Ahnert P, Schober R, Bauer M, Kirsten H, Koschny R, Meixensberger J, Krupp W: Multiple meningioma with different grades of malignancy: case report with genetic analysis applying single-nucleotide polymorphism array and classical cytogenetics. Pathol. Res. Pract. 2011, 207:67-72. (source)
  • Dänzer S, Freitag S, Beyersdorff D, Scholz M, Burgert O, Stolzenburg J: Segmentierung der Prostata aus MRT-Bilddaten mittels eines statistischen Modells. Bildverarbeitung für die Medizin 2011:114-118. (source)
  • 2010


  • Wess C, Sarnthein J, Krayenbühl N, Scholz M, Kunze E, Meixensberger J: Spectral iEEG markers precede SSEP events during surgery for subarachnoid hemorrhage. Clin Neurophysiol 2010, 121:2172-2176. (source)
  • Holland H, Koschny T, Ahnert P, Meixensberger J, Koschny R: WHO grade-specific comparative genomic hybridization pattern of astrocytoma - a meta-analysis. Pathol. Res. Pract. 2010, 206:663-668. (source)
  • Teupser D, Baber R, Ceglarek U, Scholz M, Illig T, Gieger C, Holdt LM, Leichtle A, Greiser KH, Huster D, Linsel-Nitschke P, Schäfer A, Braund PS, Tiret L, Stark K, Raaz-Schrauder D, Fiedler GM, Wilfert W, Beutner F, Gielen S, Grosshennig A, König IR, Lichtner P, Heid IM, Kluttig A, El Mokhtari, Nour E, Rubin D, Ekici AB, Reis A, Garlichs CD et al.: Genetic regulation of serum phytosterol levels and risk of coronary artery disease. Circ Cardiovasc Genet 2010, 3:331-339. (source)
  • Walther T, Schuler G, Borger MA, Kempfert J, Seeburger J, Rückert Y, Ender J, Linke A, Scholz M, Falk V, Mohr FW: Transapical aortic valve implantation in 100 consecutive patients: comparison to propensity-matched conventional aortic valve replacement. Eur. Heart J. 2010, 31:1398-1403. (source)
  • Scholz M, Gross A, Loeffler M: A biomathematical model of human thrombopoiesis under chemotherapy. Journal of Theoretical Biology 2010, 264:287-300. (source)
  • Koschny R, Holland H, Sykora J, Erdal H, Krupp W, Bauer M, Bockmuehl U, Ahnert P, Meixensberger J, Stremmel W, Walczak H, Ganten TM: Bortezomib sensitizes primary human esthesioneuroblastoma cells to TRAIL-induced apoptosis. J. Neurooncol. 2010, 97:171-185. (source)
  • Holdt LM, Beutner F, Scholz M, Gielen S, Gäbel G, Bergert H, Schuler G, Thiery J, Teupser D: ANRIL expression is associated with atherosclerosis risk at chromosome 9p21. Arterioscler. Thromb. Vasc. Biol. 2010, 30:620-627. (source)
  • Kranz A, Wagner D, Kamprad M, Scholz M, Schmidt UR, Nitzsche F, Aberman Z, Emmrich F, Riegelsberger U, Boltze J: Transplantation of placenta-derived mesenchymal stromal cells upon experimental stroke in rats. Brain Res. 2010, 1315:128-136. (source)
  • Scholz M, Hasenclever D: Comparison of estimators for measures of linkage disequilibrium. Int J Biostat 2010, 6:Article 1. (source)
  • 2009


  • López Herráez D, Bauchet M, Tang K, Theunert C, Pugach I, Li J, Nandineni MR, Gross A, Scholz M, Stoneking M: Genetic variation and recent positive selection in worldwide human populations: evidence from nearly 1 million SNPs. PLOS ONE 2009, 4:e7888. (source)
  • Burkhardt J, Petit-Teixeira E, Teixeira VH, Kirsten H, Garnier S, Ruehle S, Oeser C, Wolfram G, Scholz M, Migliorini P, Balsa A, Westhovens R, Barrera P, Alves H, Pascual-Salcedo D, Bombardieri S, Dequeker J, Radstake TR, van Riel P, van de Putte, Leo, Bardin T, Prum B, Buchegger-Podbielski U, Emmrich F, Melchers I, Cornelis F, Ahnert P: Association of the X-chromosomal genes TIMP1 and IL9R with rheumatoid arthritis. J. Rheumatol. 2009, 36:2149-2157. (source)
  • Scholz M, Engel C, Apt D, Sankar SL, Goldstein E, Loeffler M: Pharmacokinetic and pharmacodynamic modelling of the novel human granulocyte colony-stimulating factor derivative Maxy-G34 and pegfilgrastim in rats. Cell Prolif. 2009, 42:823-837. (source)
  • Scholz M, Ackermann M, Engel C, Emmrich F, Loeffler M, Kamprad M: A pharmacokinetic model of filgrastim and pegfilgrastim application in normal mice and those with cyclophosphamide-induced granulocytopaenia. Cell Prolif. 2009, 42:813-822. (source)
  • Scholz M, Ackermann M, Emmrich F, Loeffler M, Kamprad M: Effectiveness of cytopenia prophylaxis for different filgrastim and pegfilgrastim schedules in a chemotherapy mouse model. Biologics 2009, 3:27-37. (source)
  • Wilcke A, Weissfuss J, Kirsten H, Wolfram G, Boltze J, Ahnert P: The role of gene DCDC2 in German dyslexics. Ann Dyslexia 2009, 59:1-11. (source)
  • Fassl J, Walther T, Groesdonk HV, Kempfert J, Borger MA, Scholz M, Mukherjee C, Linke A, Schuler G, Mohr FW, Ender J: Anesthesia management for transapical transcatheter aortic valve implantation: a case series. J. Cardiothorac. Vasc. Anesth. 2009, 23:286-291. (source)
  • Rehak M, Müller M, Scholz M, Wiercinska J, Niederwieser D, Wiedemann P: Antiphospholipidsyndrom und retinale venöse Verschlüsse. Metaanalyse publizierter Studien. Ophthalmologe 2009, 106:427-434. (source)
  • Kirsten H, Petit-Teixeira E, Scholz M, Hasenclever D, Hantmann H, Heider D, Wagner U, Sack U, Hugo Teixeira V, Prum B, Burkhardt J, Pierlot C, Emmrich F, Cornelis F, Ahnert P: Association of MICA with rheumatoid arthritis independent of known HLA-DRB1 risk alleles in a family-based and a case control study. Arthritis Res. Ther. 2009, 11:R60. (source)
  • Kirsten H, Petit-Teixeira E, Hantmann H, Reichardt J, Burkhardt J, Emmrich F, Cornelis F, Ahnert P: A family-based study does not support the association of a functional polymorphism in the gene for endothelial nitric oxide synthase with risk for rheumatoid arthritis. Scand. J. Rheumatol. 2009, 38:320-321. (source)
  • Kirsten H, Burkhardt J, Hantmann H, Hunzelmann N, Vaith P, Ahnert P, Melchers I: 5HT2A polymorphism His452Tyr in a German Caucasian systemic sclerosis population. Arthritis Res. Ther. 2009, 11:403; author reply 404. (source)
  • Häntschel D, Fassl J, Scholz M, Sommer M, Funkat A, Wittmann M, Ender J: Leipziger "Fast-track"-Protokoll in der Kardioanästhesie. Effektiv, sicher und ökonomisch sinnvoll. Anaesthesist 2009, 58:379-386. (source)
  • Jaen O, Petit-Teixeira E, Kirsten H, Ahnert P, Semerano L, Pierlot C, Cornelis F, Boissier M, Falgarone G: No evidence of major effects in several Toll-like receptor gene polymorphisms in rheumatoid arthritis. Arthritis Res. Ther. 2009, 11:R5. (source)
  • 2008


  • Melchers I, Ahnert P: Zur Bedeutung der Genvariante PTPN22 620W für die Rheumatologie. Z Rheumatol 2008, 67:593-595. (source)
  • Reich DM, Hau S, Stahl T, Scholz M, Naumann W, Emmrich F, Boltze J, Kamprad M: Neuronal hypoxia in vitro: investigation of therapeutic principles of HUCB-MNC and CD133+ stem cells. BMC Neurosci 2008, 9:91. (source)
  • Krupp W, Holland H, Koschny R, Bauer M, Schober R, Kirsten H, Livrea M, Meixensberger J, Ahnert P: Genome-wide genetic characterization of an atypical meningioma by single-nucleotide polymorphism array-based mapping and classical cytogenetics. Cancer Genet. Cytogenet. 2008, 184:87-93. (source)
  • Kirsten H, Blume M, Emmrich F, Hunzelmann N, Mierau R, Rzepka R, Vaith P, Witte T, Melchers I, Ahnert P: No association between systemic sclerosis and C77G polymorphism in the human PTPRC (CD45) gene. J. Rheumatol. 2008, 35:1817-1819. (source)
  • Ender J, Borger MA, Scholz M, Funkat A, Anwar N, Sommer M, Mohr FW, Fassl J: Cardiac surgery fast-track treatment in a postanesthetic care unit: six-month results of the Leipzig fast-track concept. Anesthesiology 2008, 109:61-66. (source)
  • Rehak M, Rehak J, Müller M, Faude S, Faude F, Siegemund A, Krcova V, Slavik L, Hasenclever D, Scholz M, Wiedemann P: The prevalence of activated protein C (APC) resistance and factor V Leiden is significantly higher in patients with retinal vein occlusion without general risk factors. Case-control study and meta-analysis. Thromb. Haemost. 2008, 99:925-929. (source)
  • Hau S, Reich DM, Scholz M, Naumann W, Emmrich F, Kamprad M, Boltze J: Evidence for neuroprotective properties of human umbilical cord blood cells after neuronal hypoxia in vitro. BMC Neurosci 2008, 9:30. (source)
  • Scholz M, Niesch H, Steffen O, Ernst B, Loeffler M, Witruk E, Schwarz H: Impact of chess training on mathematics performance and concentration ability of children with learning disabilities. International Journal of Special Education 2008, 23. (source)
  • 2007


  • Holland H, Koschny R, Krupp W, Meixensberger J, Bauer M, Schober R, Kirsten H, Ganten TM, Ahnert P: Cytogenetic and molecular biological characterization of an adult medulloblastoma. Cancer Genet. Cytogenet. 2007, 178:104-113. (source)
  • Koschny R, Holland H, Sykora J, Haas TL, Sprick MR, Ganten TM, Krupp W, Bauer M, Ahnert P, Meixensberger J, Walczak H: Bortezomib sensitizes primary human astrocytoma cells of WHO grades I to IV for tumor necrosis factor-related apoptosis-inducing ligand-induced apoptosis. Clin. Cancer Res. 2007, 13:3403-3412. (source)
  • Kirsten H, Teupser D, Weissfuss J, Wolfram G, Emmrich F, Ahnert P: Robustness of single-base extension against mismatches at the site of primer attachment in a clinical assay. J. Mol. Med. 2007, 85:361-369. (source)
  • Tönjes A, Scholz M, Fasshauer M, Kratzsch J, Rassoul F, Stumvoll M, Blüher M: Beneficial effects of a 4-week exercise program on plasma concentrations of adhesion molecules. Diabetes Care 2007, 30:e1. (source)
  • Holland H, Koschny R, Krupp W, Meixensberger J, Bauer M, Kirsten H, Ahnert P: Comprehensive cytogenetic characterization of an esthesioneuroblastoma. Cancer Genet. Cytogenet. 2007, 173:89-96. (source)
  • Mahr S, Kirsten H, Mueller B: Reply to Loughlin et al. Am J Hum Genet 2007, 80:386-387. (source)
  • Ahnert P, Kirsten H: Association of ITGAV supports a role of angiogenesis in rheumatoid arthritis. Arthritis Res. Ther. 2007, 9:108. (source)
  • 2006


  • Tönjes A, Scholz M, Loeffler M, Stumvoll M: Association of Pro12Ala polymorphism in peroxisome proliferator-activated receptor gamma with Pre-diabetic phenotypes: meta-analysis of 57 studies on nondiabetic individuals. Diabetes Care 2006, 29:2489-2497. (source)
  • Scholz M, Engel C, Loeffler M: Model-based design of chemotherapeutic regimens that account for heterogeneity in leucopoenia. Br. J. Haematol. 2006, 132:723-735. (source)
  • Kirsten H, Dienst S, Emmrich F, Ahnert P: CalcDalton: a tool for multiplex genotyping primer design for single-base extension reactions using cleavable primers. BioTechniques 2006, 40:158, 160, 162. (source)
  • Last updated: 08-Oct-2015 Time: 0.15 s