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Institute of Human Genetics
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Overview
Publications
(729)
Research Grants
(48)
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Journal article
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Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1 (2015)
Cheng THT, Thompson D, Painter J, O'Mara T, Gorman M, Martin L, Palles C, et al.
Journal article
MAP4-dependent regulation of microtubule formation affects centrosome, cilia, and golgi architecture as a central mechanism in growth regulation (2015)
Zahnleiter D, Hauer N, Keßler K, Uebe S, Sugano Y, Neuhauss SCF, Gießl A, et al.
Journal article
Inhibition of RAS activation due to a homozygous ezrin variant in patients with profound intellectual disability (2015)
Riecken LB, Tawamie H, Dornblut C, Buchert R, Ismayel A, Schulz A, Schumacher J, et al.
Journal article
Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer (2015)
Lawrenson K, Li Q, Kar S, Seo JH, Tyrer J, Spindler TJ, Lee J, et al.
Journal article
The temporal expression pattern of alpha-synuclein modulates olfactory neurogenesis in transgenic mice (2015)
Schreglmann SR, Regensburger M, Rockenstein E, Masliah E, Xiang W, Winkler J, Winner B
Journal article
Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk (2015)
Chornokur G, Lin HY, Tyrer JP, Lawrenson K, Dennis J, Amankwah EK, Qu X, et al.
Journal article
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk (2015)
Carvajal-Carmona LG, O'Mara TA, Painter JN, Lose FA, Dennis J, Michailidou K, Tyrer JP, et al.
Journal article
Association of genetic and psychological factors with persistent pain after cosmetic thoracic surgery (2015)
Dimova V, Loetsch J, Hühne K, Winterpacht A, Heesen M, Parthum A, Weber PG, et al.
Journal article
Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8 (2015)
Boycott KM, Beaulieu CL, Kernohan KD, Gebril OH, Mhanni A, Chudley AE, Redl D, et al.
Journal article
Pattern of Functional TTX-Resistant Sodium Channels Reveals a Developmental Stage of Human iPSC- and ESC-Derived Nociceptors (2015)
Eberhardt E, Havlicek S, Schmidt D, Link A, Neacsu C, Kohl Z, Hampl M, et al.
Journal article
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