S. Gerber

6.8k citations
99 papers · 4.3k · h-index 35

Impact in

  • Ophthalmology top 0.5%
    • Retinal Diseases and Treatments
  • Molecular Biology top 2%
    • Retinal Development and Disorders
    • Mitochondrial Function and Pathology

Papers in

  • Molecular Biology 56
    • Retinal Development and Disorders 36
    • Mitochondrial Function and Pathology 8
    • Retinoids in leukemia and cellular processes 5
  • Ophthalmology 26
    • Retinal Diseases and Treatments 23
Co-authors
Jean‐Michel Rozet (67 shared papers)Josseline Kaplan (61 shared papers)Isabelle Perrault (39 shared papers)Antoine Kremer (8 shared papers)Jean‐Louis Dufier (27 shared papers)Dominique Ducroq (19 shared papers)Arnold Münnich (28 shared papers)Hélène Dollfus (12 shared papers)
Journals
Journal of Medical Genetics (8 papers)Human Mutation (6 papers)Human Genetics (5 papers)European Journal of Human Genetics (5 papers)Theoretical and Applied Genetics (5 papers)
Partner nations
FranceMoroccoUnited Kingdom

In The Last Decade

S. Gerber

96 papers receiving 4.1k citations

Peers

S. Gerber
Comparison fields: 5 of 111
  • Ophthalmology 997
  • Molecular Biology 2.8k
  • Genetics 1.0k
  • Sensory Systems 157
  • Nature and Landscape Conservation 385
Replace James M. Fadool with:
James M. Fadool United States
Felix Loosli Germany
E. Fujimoto United States
Hironori Wada Japan
Lucia Manni Italy
John S. Taylor Canada
Douglas O. Clary United States
Christoph Winkler Germany
Paula E. May United States
Anders Fjose Norway
S. Gerber relative to James M. Fadool United States James M. Fadool's profile →
Citations per field
00.5×2×4×6.1×
James M. Fadool · 1×
Citations per year

Countries citing papers authored by S. Gerber

Since Specialization
Citations

This map shows the geographic impact of S. Gerber'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 S. Gerber with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. Gerber more than expected).

Fields of papers citing papers by S. Gerber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. Gerber. 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 S. Gerber. The network helps show where S. Gerber may publish in the future.

Co-authors

The 25 scholars most cited alongside S. Gerber, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with S. Gerber Line = papers co-authored together S. Gerber links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 99 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Retinal–specific guanylate cyclase gene mutations in Leber's congenital amaurosis
Nature Genetics ·Isabelle Perrault, Jean‐Michel Rozet, Patrick Calvas, S. Gerber, Agnès Camuzat, Hélène Dollfus, Sophie Châtelin, Eric H. Souied, Ihmad Ghazi, Corinne Leowski, Michel Bonnemaison, Denis Le Paslier, J Frézal, Jean‐Louis Dufier, Steven J. Pittler, Arnold Munnich, Josseline Kaplan
1996383
2
Species relative abundance and direction of introgression in oaks
Molecular Ecology ·Olivier Lepais, Rémy J. Petit, Erwan Guichoux, Jessica E. Lavabre, Florian J. Alberto, Antoine Kremer, S. Gerber
2009298
3
Leber congenital amaurosis: Comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecular diagnosis
Human Mutation ·Sylvain Hanein, Isabelle Perrault, S. Gerber, Gaëlle Tanguy, Fabienne Barbet, Dominique Ducroq, Patrick Calvas, Hélène Dollfus, Christian Hamel, Tuija Löppönen, Francis L. Munier, Louisa Santos, Stavit A. Shalev, Dimitrios Zafeiriou, Jean‐Louis Dufier, Arnold Munnich, Jean‐Michel Rozet, Josseline Kaplan
2004292
4
Comparison of microsatellites and amplified fragment length polymorphism markers for parentage analysis
Molecular Ecology ·S. Gerber, Stéphanie Mariette, R. Streiff, Catherine Bodénès, Antoine Kremer
2000224
5
famoz: a software for parentage analysis using dominant, codominant and uniparentally inherited markers
Molecular Ecology Notes ·S. Gerber, Patrick Chabrier, Antoine Kremer
2003199
6
Retinal Dehydrogenase 12 (RDH12) Mutations in Leber Congenital Amaurosis
The American Journal of Human Genetics ·Isabelle Perrault, Sylvain Hanein, S. Gerber, Fabienne Barbet, Dominique Ducroq, Hélène Dollfus, Christian Hamel, Jean‐Louis Dufier, Arnold Munnich, Josseline Kaplan, Jean‐Michel Rozet
2004158
7
A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1
Nature Genetics ·Josseline Kaplan, S. Gerber, Dominique Larget‐Piet, Jean‐Michel Rozet, Hélène Dollfus, Jean-Louis Dufier, Sylvie Odent, Anne Postel-Vinay, Nicolas Janin, Marie‐Louise Briard, J Frézal, Arnold Munnich
1993144
8
Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis
European Journal of Human Genetics ·S. Gerber, Isabelle Perrault, Sylvain Hanein, Fabienne Barbet, Dominique Ducroq, Imad Ghazi, Dominique Martin‐Coignard, Corinne Leowski, Tessa Homfray, Jean‐Louis Dufier, Arnold Münnich, Josseline Kaplan, Jean‐Michel Rozet
2001134
9
Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies
European Journal of Human Genetics ·Jean‐Michel Rozet, S. Gerber, Eric H. Souied, Isabelle Perrault, Sophie Châtelin, Imad Ghazi, Corinne Leowski, Jean‐Louis Dufier, Arnold Munnich, Josseline Kaplan
1998130
10
A gene for usher syndrome type I (USH1A) maps to chromosome 14q
Genomics ·Josseline Kaplan, S. Gerber, Dominique Bonneau, Jean‐Michel Rozet, O. Delrieu, Marie‐Louise Briard, Hélène Dollfus, Imad Ghazi, Jean‐Louis Dufier, J Frézal, Arnold Münnich
1992120
11
Leber Congenital Amaurosis
Molecular Genetics and Metabolism ·Isabelle Perrault, Jean‐Michel Rozet, S. Gerber, (unknown), Corinne Leowski, Dominique Ducroq, Eric H. Souied, (unknown), Arnold Münnich, Josseline Kaplan
1999117
12
Leaf morphological analyses in four European oak species ( Quercus ) and their hybrids: A comparison of traditional and geometric morphometric methods
Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology ·Vincenzo Viscosi, Olivier Lepais, S. Gerber, Paola Fortini
200999
13
Spectrum of retGC1 mutations in Leber's congenital amaurosis
European Journal of Human Genetics ·Isabelle Perrault, Jean‐Michel Rozet, S. Gerber, Imad Ghazi, Dominique Ducroq, Eric H. Souied, Corinne Leowski, Michèle Bonnemaison, Jean‐Louis Dufier, Arnold Münnich, Josseline Kaplan
200098
14
Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus
Journal of Medical Genetics ·Jean‐Michel Rozet, S. Gerber, Imad Ghazi, Isabelle Perrault, Dominique Ducroq, Eric Souied, Annick Cabot, J.L. Dufier, A Munnich, Josseline Kaplan
199978
15
Gene flow estimation with microsatellites in a Malagasy seed orchard of Eucalyptus grandis
Theoretical and Applied Genetics ·Gilles Chaix, S. Gerber, Vololoniriana Razafimaharo, P. Vigneron, Daniel Verhaegen, Serge Hamon
200376
16
Seed gene flow and fine-scale structure in a Mediterranean pine (Pinus pinaster Ait.) using nuclear microsatellite markers
Theoretical and Applied Genetics ·Santiago C. González‐Martínez, S. Gerber, M. Cervera, José M. Martı́nez-Zapater, Luis Gil, Ricardo Alı́a
200275
17
Mutations in the tricarboxylic acid cycle enzyme, aconitase 2, cause either isolated or syndromic optic neuropathy with encephalopathy and cerebellar atrophy
Journal of Medical Genetics ·Metodi D. Metodiev, S. Gerber, Laurence Hubert, Agnès Delahodde, Dominique Chrétien, Xavier Gérard, Patrizia Amati‐Bonneau, Marie-Christine Giacomotto, Nathalie Boddaert, Anna Kamińska, Isabelle Desguerre, Jeanne Amiel, Marlène Rio, Josseline Kaplan, Arnold Münnich, Agnès Rötig, Jean‐Michel Rozet, Claude Besmond
201474
18
TMEM126A, Encoding a Mitochondrial Protein, Is Mutated in Autosomal-Recessive Nonsyndromic Optic Atrophy
The American Journal of Human Genetics ·Sylvain Hanein, Isabelle Perrault, Olivier Roche, S. Gerber, Noman Khadom, Marlène Rio, Nathalie Boddaert, Marc Jeanpierre, Nora Brahimi, Valérie Serre, Dominique Chrétien, Nathalie Delphin, Lucas Fares‐Taie, Sahran Lachheb, Agnès Rötig, Françoise Meire, Arnold Münnich, Jean‐Louis Dufier, Josseline Kaplan, Jean‐Michel Rozet
200972
19
The photoreceptor cell-specific nuclear receptor gene ( PNR ) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition
Human Genetics ·S. Gerber, Jean‐Michel Rozet, Shinichiro Takezawa, Luísa Coutinho Santos, Lucilia Lopes, Olivier Gribouval, Clotilde Penet, Isabelle Perrault, Dominique Ducroq, Eric H. Souied, Marc Jeanpierre, Serge Romana, J Frézal, Fernando Ferraz, Ruth Yu-Umesono, Arnold Münnich, Josseline Kaplan
200071
20
A Gene for X-Linked Idiopathic Congenital Nystagmus (NYS1) Maps to Chromosome Xp11.4-p11.3
The American Journal of Human Genetics ·Annick Cabot, Jean‐Michel Rozet, S. Gerber, Isabelle Perrault, Dominique Ducroq, Asma Smahi, Eric H. Souied, Arnold Munnich, Josseline Kaplan
199969

About S. Gerber

S. Gerber is a scholar working on Molecular Biology, Ophthalmology, Genetics, Nature and Landscape Conservation and Radiology, Nuclear Medicine and Imaging, having authored 99 papers that have together received 4.3k indexed citations. Recurring topics across this work include Retinal Development and Disorders (36 papers), Retinal Diseases and Treatments (23 papers), Genetic diversity and population structure (8 papers), Mitochondrial Function and Pathology (8 papers), Genetic Mapping and Diversity in Plants and Animals (7 papers), Ecology and Vegetation Dynamics Studies (6 papers), Plant and animal studies (6 papers) and Retinoids in leukemia and cellular processes (5 papers). The work is most often cited by research in Ophthalmology (997 citations), Molecular Biology (2.8k citations), Genetics (1.0k citations), Sensory Systems (157 citations) and Nature and Landscape Conservation (385 citations). S. Gerber has collaborated with scholars based in France, Morocco and United Kingdom. Frequent co-authors include Jean‐Michel Rozet, Josseline Kaplan, Isabelle Perrault, Antoine Kremer, Jean‐Louis Dufier, Dominique Ducroq, Arnold Münnich, Hélène Dollfus, Olivier Lepais and Arnold Munnich. Their work appears in journals such as Journal of Medical Genetics, Human Mutation, Human Genetics, European Journal of Human Genetics and Theoretical and Applied Genetics.

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.

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