Andrea Gehrig - Concepedia

Author

Andrea Gehrig

Also Known As

A Gehrig, A. Gehrig, Alfons Meindl, Andrea E. Gehrig, Andrea Gehrig, Davidson, Rosemarie, Debra Frost, Eitan Friedman, Gehrig, A, Gehrig, A.

101

Publications

5.2K

Citations

H-Index

Concepts

All Affiliations

University of Würzburg University Hospital Cologne Leipzig University Heinrich Heine University Düsseldorf Medizinische Hochschule Hannover

About

Andrea Gehrig is an author at University of Würzburg specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	15	1.2K
2	Engineering	2	2	47
3	Public Health	2	2	174
4	Natural Sciences	1	1	33
5	Biochemistry	1	1	33

Andrea Gehrig

Publications

3.7K

Citations

H-Index

Page 1

	Year	Citations
Positional cloning of the gene associated with X-linked juvenile retinoschisis Christian Sauer, Andrea Gehrig, Regina Warneke-Wittstock, Nature Genetics BiologyDevelopmental GeneticsGeneticsCraniofacial DevelopmentGenetic Mechanism	1997	492
Association of Type and Location of<i>BRCA1</i>and<i>BRCA2</i>Mutations With Risk of Breast and Ovarian Cancer Timothy R. Rebbeck, Nandita Mitra, Fei Wan, JAMA	2015	484
Prevalence of <i>BRCA1/2</i> germline mutations in 21 401 families with breast and ovarian cancer Karin Kast, Kerstin Rhiem, Barbara Wappenschmidt, Journal of Medical Genetics	2016	217
Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration Franziska Krämer, Karen L. White, Daniel Pauleikhoff, European Journal of Human Genetics Ocular DiseaseMendelian DisorderOphthalmologyGenetic DisorderGenetics	2000	214
Inactivation of the murine X-linked juvenile retinoschisis gene, Rs1h, suggests a role of retinoschisin in retinal cell layer organisation and synaptic structure Heinrich Schrewe, Andrea Gehrig, Christoph Friedburg, University of Birmingham Research Portal (University of Birmingham)	2002	211
Gene panel testing of 5589 <i><scp>BRCA</scp>1/2</i>‐negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer Jan Hauke, Judit Horváth, Eva Groß, Cancer Medicine	2018	161
Large scale multifactorial likelihood quantitative analysis of <i>BRCA1</i> and <i>BRCA2</i> variants: An ENIGMA resource to support clinical variant classification Michael T. Parsons, Emma Tudini, Hongyan Li, Human Mutation GeneticsGenetic EpidemiologyPathologyMultifactorial Likelihood AnalysisDisease Gene Identification	2019	148
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants Daniel R. Barnes, Matti A. Rookus, Lesley McGuffog, Genetics in Medicine	2020	137
Constitutive promoter methylation of BRCA1 and RAD51C in patients with familial ovarian cancer and early-onset sporadic breast cancer T. Hansmann, Galyna Pliushch, Monika Leubner, Human Molecular Genetics	2012	135
BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer Nana Weber‐Lassalle, Jan Hauke, Juliane Ramser, Breast Cancer Research	2018	127

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