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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
(7)
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Journal article
Journal article
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Book chapter / Article in edited volumes
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Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome (2023)
Hirbo JB, Pasutto F, Gamazon ER, Evans P, Pawar P, Berner D, Sealock J, et al.
Journal article
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry (2023)
Mueller SH, Lai AG, Valkovskaya M, Michailidou K, Bolla MK, Wang Q, Dennis J, et al.
Journal article
Differential Effects of Ontamalimab Versus Vedolizumab on Immune Cell Trafficking in Intestinal Inflammation and Inflammatory Bowel Disease (2023)
Schulze L, Becker E, Dedden M, Liu L, Van Passen C, Mohamed Abdou M, Müller T, et al.
Journal article
Differential Effects of Very-Low-Volume Exercise Modalities on Telomere Length, Inflammation, and Cardiometabolic Health in Obese Metabolic Syndrome Patients: A Subanalysis from Two Randomized Controlled Trials (2023)
Reljic D, Koller A, Herrmann HJ, Ekici AB, Neurath M, Zopf Y
Journal article
Impact of Microbiome–Brain Communication on Neuroinflammation and Neurodegeneration (2023)
Stolzer I, Scherer E, Süß P, Rothhammer V, Winner B, Neurath M, Günther C
Journal article, Review article
Human Induced Pluripotent Stem Cell-Derived Pericytes as Scalable and Editable Source to Study Direct Lineage Reprogramming Into Induced Neurons (2023)
Menon R, Petrucci L, Lohrer B, Zhang J, Schulze M, Schichor C, Winner B, et al.
Journal article
Ex Vivo Chromosomal Radiosensitivity Testing in Patients with Pathological Germline Variants in Breast Cancer High-Susceptibility Genes BReast CAncer 1 and BReast CAncer 2 (2023)
Zuhair Kassem T, Wunderle M, Kuhlmann L, Rübner M, Hübner H, Hoyer J, Reis A, et al.
Journal article
Scaffold-Based (Matrigel™) 3D Culture Technique of Glioblastoma Recovers a Patient-like Immunosuppressive Phenotype (2023)
Braun FK, Rothhammer-Hampl T, Lorenz J, Pohl S, Menevse AN, Vollmann-Zwerenz A, Bumes E, et al.
Journal article
LHX2 haploinsufficiency causes a variable neurodevelopmental disorder (2023)
Schmid CM, Gregor A, Costain G, Morel CF, Massingham L, Schwab J, Quélin C, et al.
Journal article
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis (2023)
Gehin C, Lone MA, Lee W, Capolupo L, Ho S, Adeyemi AM, Gerkes EH, et al.
Journal article
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