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Scientific Reports|January 20, 2022
Genome and transcriptome profiling of spontaneous preterm birth phenotypesJuhi K Gupta, Angharad Care, Laura Goodfellow, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 8, 2015
ABCB1 gene variants and antidepressant treatment outcome: A meta-analysisBarbara Breitenstein, Tanja Maria Brückl, Marcus Ising, et al.Human Genetics|August 14, 2012
A beginners guide to SNP calling from high-throughput DNA-sequencing dataAndré Altmann, Peter Weber, Daniel Bader, et al.Journal of Glaucoma|April 18, 2009
Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucomaChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.Journal of Psychiatric Research|June 1, 2012
ANK3 and CACNA1C--missing genetic link for bipolar disorder and major depressive disorder in two German case-control samplesStefan Kloiber, Darina Czamara, Nazanin Karbalai, et al.BMC Medical Genetics|September 17, 2009
Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control studyChristiane Wolf, Eugen Gramer, Bertram Müller-Myhsok, et al.Bioinformatics (Oxford, England)|June 21, 2011
vipR: variant identification in pooled DNA using RAndre Altmann, Peter Weber, Carina Quast, et al.Journal of Electromyography and Kinesiology : Official Journal of the International Society of Electrophysiological Kinesiology|April 9, 2013
Maximality of shoulder external rotation effort in patients presenting with work related injury: the clinical applicability of the DEC parameterJoaquim Chaler, Eduard Pujol, Carme Unyó, et al.Plos One|May 19, 2012
Evidence for the late MMN as a neurophysiological endophenotype for dyslexiaNina Neuhoff, Jennifer Bruder, Jürgen Bartling, et al.American Journal of Human Genetics|April 16, 2002
Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier geneRalf Giess, Bettina Holtmann, Massimiliano Braga, et al.Pageof 27