Andrea Gehrig

5.2k total citations
31 papers, 1.3k citations indexed

About

Andrea Gehrig is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Andrea Gehrig has authored 31 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Ophthalmology. Recurrent topics in Andrea Gehrig's work include Retinal Development and Disorders (12 papers), BRCA gene mutations in cancer (7 papers) and Retinal Diseases and Treatments (6 papers). Andrea Gehrig is often cited by papers focused on Retinal Development and Disorders (12 papers), BRCA gene mutations in cancer (7 papers) and Retinal Diseases and Treatments (6 papers). Andrea Gehrig collaborates with scholars based in Germany, United Kingdom and United States. Andrea Gehrig's co-authors include Bernhard H. F. Weber, Birgit Lorenz, Christian Sauer, Bernhard Jurklies, Andreas Marquardt, Cecil C. Ewing, Alice Gibson, Karen L. White, Heinrich Schrewe and Ernst R. Tamm and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Andrea Gehrig

30 papers receiving 1.3k citations

Peers

Countries citing papers authored by Andrea Gehrig

Since Specialization

Citations

This map shows the geographic impact of Andrea Gehrig's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Andrea Gehrig with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrea Gehrig more than expected).

Fields of papers citing papers by Andrea Gehrig

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrea Gehrig. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Andrea Gehrig. The network helps show where Andrea Gehrig may publish in the future.

Co-authorship network of co-authors of Andrea Gehrig

This figure shows the co-authorship network connecting the top 25 collaborators of Andrea Gehrig. A scholar is included among the top collaborators of Andrea Gehrig based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Andrea Gehrig. Andrea Gehrig is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Aktualisierte Kriterien des Deutschen Konsortiums Familiärer Brust- und Eierstockkrebs zur Klassifizierung von Keimbahn-Sequenzvarianten in Risikogenen für familiären Brust- und Eierstockkrebs 2021 ·Senologie - Zeitschrift für Mammadiagnostik und -therapie ·Jan Hauke, Barbara Wappenschmidt, Ulrike Faust, Dieter Niederacher, Lisa Wiesmüller, Gunnar Schmidt, (unknown), Alfons Meindl, Andrea Gehrig, Christian Sutter, Juliane Ramser, Andreas Rump, (unknown)	3
2	Targeted molecular analysis in adrenocortical carcinomas: a way towards improved personalized prognostication 2018 ·Endocrine Abstracts ·(unknown), Silke Appenzeller, (unknown), Silviu Sbiera, Stefan Kircher, Barbara Altieri, Indrajit Nanda, Isabel Weigand, Andrea Gehrig, Sonja Steinhauer, (unknown), Matthias Kroiß, Simone Rost, Andreas Rosenwald, Martin Faßnacht, Cristina L. Ronchi	1
3	Deep intronic variants introduce DMD pseudoexon in patient with muscular dystrophy 2017 ·Neuromuscular Disorders ·(unknown), (unknown), Andrea Gehrig, Heike Kölbel, Ulrike Schara, Wolfram Kreß, Simone Rost	17
4	Constitutive promoter methylation of BRCA1 and RAD51C in patients with familial ovarian cancer and early-onset sporadic breast cancer 2012 ·Human Molecular Genetics ·T. Hansmann, Galyna Pliushch, (unknown), (unknown), Daniela Endt, Andrea Gehrig, Sabine Preisler-Adams, Peter Wieacker, (unknown)	74
5	Analysis of F8 mRNA in haemophilia A patients with silent mutations or presumptive splice site mutations 2012 ·Haemophilia ·Marcel Zimmermann, Andrea Gehrig, Johannes Oldenburg, C. R. Müller, Simone Rost	15
6	Mutation screening of the RYR1-cDNA from peripheral B-lymphocytes in 15 Swedish malignant hyperthermia index cases 2009 ·British Journal of Anaesthesia ·Marcus Broman, Andrea Gehrig, Gunilla Islander, Mikael Bodelsson, Eva Ranklev-Twetman, Henrik Rüffert, C. R. Müller	13
7	The role of caspases in photoreceptor cell death of the retinoschisin-deficient mouse 2006 ·Cytogenetic and Genome Research ·Andrea Gehrig, Andreas Janßen, Frank Horling, Christian Grimm, Bernhard H. F. Weber	17
8	PTEN mutations do not cause nuclear β-catenin accumulation in endometrial carcinomas 2004 ·Human Pathology ·Barbara Wappenschmidt, Eva Wardelmann, Andrea Gehrig, Thomas Schöndorf, Nicolaì Maass, G. Bonatz, A. M. Gassel, Torsten Pietsch, Peter Mallmann, Bernhard H. F. Weber, Rita K. Schmutzler	14
9	Identifying differentially expressed genes in the mammalian retina and the retinal pigment epithelium by suppression subtractive hybridization 2004 ·Cytogenetic and Genome Research ·Heidi L. Schulz, (unknown), (unknown), (unknown), Andrea Gehrig, Bernhard H. F. Weber	10
10	Inactivation of the murine X-linked juvenile retinoschisis gene, Rs1h, suggests a role of retinoschisin in retinal cell layer organisation and synaptic structure 2002 ·University of Birmingham Research Portal (University of Birmingham) ·Bernhard H. F. Weber, Heinrich Schrewe, Laurie L. Molday, Andrea Gehrig, Karen L. White, Mathias W. Seeliger, Gesine B. Jaissle, Christoph Friedburg, Ernst R. Tamm, Robert S. Molday	181
11	EST mining of the UniGene dataset to identify retina-specific genes 2000 ·Cytogenetic and Genome Research ·Heidi Stöhr, Nancy Mah, Heidi L. Schulz, Andrea Gehrig, (unknown), Bernhard H. F. Weber	21
12	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 2000 ·European Journal of Human Genetics ·Franziska Krämer, Karen L. White, Daniel Pauleikhoff, Andrea Gehrig, Lori A. Passmore, Andrea Rivera, Günther Rudolph, Ulrich Kellner, Monika Andrassi, Birgit Lorenz, Klaus Rohrschneider, A. Blankenagel, Bernhard Jurklies, H Schilling, F. Schütt, Frank G. Holz, Bernhard H. F. Weber	169
13	Assessment of RS1 in X‐linked juvenile retinoschisis and sporadic senile retinoschisis 1999 ·Clinical Genetics ·Andrea Gehrig, Karen L. White, Birgit Lorenz, Monika Andrassi, Stefan Clemens, Bernhard H. F. Weber	13
14	Isolation and characterization of the murine X-linked juvenile retinoschisis ( Rs1h ) gene 1999 ·Mammalian Genome ·Andrea Gehrig, (unknown), Christian Sauer, Bernhard H. F. Weber	27
15	Mapping and genomic characterization of the gene encoding diacylglycerol kinase γ ( DAGK3 ): assessment of its role in dominant optic atrophy ( OPA1 ) 1999 ·Human Genetics ·Heidi Stöhr, (unknown), Andrea Gehrig, Michael Köehler, Bernhard Jurklies, Ulrich Kellner, Beate Leo‐Kottler, Michael Schmid, Bernhard H. F. Weber	6
16	Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies 1998 ·Cytogenetic and Genome Research ·Ute Felbor, Andrea Gehrig, Christian Sauer, Andreas Marquardt, (unknown), Markus Schmid, Bernhard H. F. Weber	17
17	Molecular defects in alkaptonuria 1997 ·Cytogenetic and Genome Research ·Andrea Gehrig, Stefan Schmidt, C R Müller, (unknown), (unknown), (unknown)	39
18	Cloning of the homogentisate 1,2-dioxygenase gene, the key enzyme of alkaptonuria in mouse 1997 ·Mammalian Genome ·Stefan Schmidt, Andrea Gehrig, Michael Köehler, Michael Schmid, C. R. Müller, (unknown)	16
19	Positional cloning of the gene associated with X-linked juvenile retinoschisis 1997 ·Nature Genetics ·Christian Sauer, Andrea Gehrig, (unknown), Andreas Marquardt, Cecil C. Ewing, Alice Gibson, Birgit Lorenz, Bernhard Jurklies, Bernhard H. F. Weber	375
20	Chondrogenesis of limb-bud cells: improved culture method and the effect of the potent teratogen retinoic acid 1985 ·Xenobiotica ·Andreas D. Kistler, (unknown), Andrea Gehrig	16

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact