Prof. Dr. med. Andre Reis

human genetics

User Score	Experience	Rating	Price Range	Publications	Online Consultations
91%	38 years	9.8/10	$$$$	1778	No

Overview

Country, City

Germany, Erlangen

Health facility

University Hospital Erlangen

Medical unit

Department of human genetics

About the doctor

Prof. Dr. med. Andre Reis is a highly experienced doctor with a specialization in human genetics. With 37 years of experience, he has established himself as a renowned expert. He works at the Department of Human Genetics at the University Hospital Erlangen in Germany. Prof. Dr. Reis has made significant contributions to human genetics throughout his career. He has published a staggering number of 1778 scientific publications, which showcase his dedication and expertise. His research focuses on various genetic disorders and diseases, including psoriasis, glaucoma, and mental retardation. His groundbreaking research projects, funded by the German Research Foundation, have led to important discoveries and advancements in understanding these conditions. Prof. Dr. Reis's extensive knowledge and expertise make him an invaluable asset in human genetics. His research dedication and numerous accomplishments have solidified his reputation as a leading authority in the field. With his wealth of experience and commitment to advancing medical knowledge, patients can trust that they receive the highest standard of care under his guidance.

Skills & Expertise

Resume

CV (Curriculum Vitae)

Education

1979-1986 Medical studies in Goettingen and Luebeck
Obtaining a license for medical practice
1986 Doctorate at the Institute for Human Genetics at the Medical University of Luebeck
1995 Habilitation and a teaching license in human genetics
1995 Obtaining specialization in human genetics

Experience

1987-1988 Research Associate at the Institute for Human Genetics at the University of Goettingen
1989-1998 University Assistant at the Institute for Human Genetics at the Charite University Hospital in Berlin
1998-2000 University Professor (C3) for medical genetics and gene mapping at the Charite University Hospital in Berlin and Group Leader at the Max Delbruck Center for Molecular Medicine Berlin-Buch
2000 Professor and Director, Department of human genetics at the University Hospital Erlangen

Awards & Memberships

1995-2000 Founder and Project Manager of the Microsatellite Center and Gene Mapping Centre at the Max Delbruck Center for Molecular Medicine
1995-1998 Project from German Research Foundation: "Isolation and characterization of the basal cell nevus syndrome-gene and analysis of the function of the gene product in development"
1996-2005 Project from German Research Foundation: "Position cloning of disposition genes for Psoriasis Vulgaris"
1999-2002 Project from German Research Foundation: "Isolation and characterization of the NBS gene"
1999-2009 Project from German Research Foundation: "Identification of genes for primary glaucoma"
2003-2007 Project from German Research Foundation: "Identification of a disease-causing gene for periodic catatonia on chromosome 15q15"
2003-2009 Project from German Research Foundation: "Genetics of pseudoexfoliation glaucoma and syndrome"
2006 Corresponding Member of the Academy of Sciences and Literature Mainz
2007 Member of the National Academy of Sciences Leopoldina
2007 Senator of the University of Erlangen-Nuremberg
2007 Speaker of the Interdisciplinary Center for Clinical Research at the University Hospital Erlangen
2008-2012 Chairman of the German Society for Human Genetics
2012 Project from German Research Foundation: "Systematic characterization of genes in autosomal recessive mental retardation"
2012-2015 Project from German Research Foundation: "Analysis of strain-specific differences in the lymphangiogenic response in the cornea to identify new endogenous modulators of lymphangiogenesis"
2015 Project from German Research Foundation: “Identification of new endogenous modulators of (inflammatory) lymphangiogenesis by analyzing strain-specific differences in the mouse model”