David Geneviève

9.3k citations

80 papers · 2.3k indexed · h-index 24

Genetics top 2%
- Genomic variations and chromosomal abnormalities 16
- Genomics and Rare Diseases 13
- Genetics and Neurodevelopmental Disorders 9
- Connective tissue disorders research 8
- Congenital Ear and Nasal Anomalies 5
- Genetic Syndromes and Imprinting 4
Molecular Biology top 5%
Genetics top 5%
- Genomic variations and chromosomal abnormalities 16
- Genomics and Rare Diseases 13
- Genetics and Neurodevelopmental Disorders 9
- Connective tissue disorders research 8
- Congenital Ear and Nasal Anomalies 5
- Genetic Syndromes and Imprinting 4
Cancer Research top 10%
Cell Biology top 5%
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 6
- Fetal and Pediatric Neurological Disorders 5

Co-authors: Valérie Cormier‐Daire Jeanne Amiel Arnold Münnich Stanislas Lyonnet Vincent Gâtinois Damien Sanlaville Michel Vekemans Loïc de Pontual
Cited by: Genetics Molecular Biology
Journals: Nature Genetics (2 papers)Journal of Clinical Oncology (1 paper)Blood (1 paper)
Partner nations: France United States United Kingdom

In The Last Decade

David Geneviève

73 papers receiving 2.3k citations

Peers

Countries citing papers authored by David Geneviève

Since Specialization

Citations

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

Fields of papers citing papers by David Geneviève

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside David Geneviève, 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 David Geneviève Line = papers co-authored together David Geneviève links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Abnormal Immune Profile in Individuals with Kabuki Syndrome Journal of Clinical Immunology ·Margot Comel,Norma Saad,Debapratim Sil,Florence Apparailly,Marjolaine Willems,Farida Djouad,Jean‐Christophe Andrau,Claire Lozano,David Geneviève	2024	1
2	Speech and language in DDX3X‐neurodevelopmental disorder: A call for early augmentative and alternative communication intervention American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Elana Forbes,Lottie D. Morison,Fatma Lelik,Tegan Howell,Simone Debono,Himanshu Goel,Pauline Burger,Jean‐Louis Mandel,David Geneviève,David J. Amor,Angela Morgan	2024	5
3	Réflexions éthiques sur le dépistage génétique préconceptionnel en population générale : le débat français et l’avis de la Société Française de Médecine Prédictive et Personnalisée Ethics Medicine and Public Health ·P. Pujol,S. Fodil-Chérif,Jean‐Louis Mandel,Bernard Baertschi,Damien Sanlaville,D. Zarca,A. Tolédano,P. Bloch,David Geneviève	2020	0
4	Pycnodysostosis: Natural history and management guidelines from 27 French cases and a literature review Clinical Genetics ·Varoona Bizaoui,Caroline Michot,Geneviève Baujat,Cyril Amouroux,S. Baron,Yline Capri,Martine Cohen‐Solal,Corinne Collet,Anne Dieux,David Geneviève,Bertrand Isidor,Sophie Monnot,Massimiliano Rossi,Anya Rothenbühler,Élise Schaefer,Valérie Cormier‐Daire	2019	31
5	TBL1XR1 mutations in Pierpont syndrome are not restricted to the recurrent p.Tyr446Cys mutation American Journal of Medical Genetics Part A ·Camille Lemattre,Julien Thévenon,Yannis Duffourd,Sophie Nambot,Emmanuelle Haquet,B. Vuadelle,David Geneviève,P. Sardá,A. L. Bruel,Paul Kuentz,Constance Wells,Laurence Faivre,Marjolaine Willems	2018	12
6	LARP7 variants and further delineation of the Alazami syndrome phenotypic spectrum among primordial dwarfisms: 2 sisters European Journal of Medical Genetics ·Marion Imbert‐Bouteille,Frédéric Tran Mau‐Them,Julien Thévenon,Thomas Guignard,Vincent Gâtinois,Jean‐Baptiste Rivière,Anne Boland,Vincent Meyer,Jean‐François Deleuze,Elodie Sanchez,Florence Apparailly,David Geneviève,Marjolaine Willems	2018	19
7	Three-dimensional computer-assisted dissection of pancreatic lymphatic anatomy on human fetuses: a step toward automatic image alignment Surgical and Radiologic Anatomy ·Thomas Bardol,Gérard Subsol,Marie-José Perez,David Geneviève,Audrey Lamouroux,B Antoine,Guillaume Captier,M. Prudhomme,Martin Bertrand	2018	3
8	TMEM187-IRAK1Polymorphisms Associated with Rheumatoid Arthritis Susceptibility in Tunisian and French Female Populations: Influence of Geographic Origin Journal of Immunology Research ·Olfa Khalifa,Nathalie Balandraud,Nathalie Lambert,Isabelle Auger,Jean Roudier,Audrey Sénéćhal,David Geneviève,Christophe Picard,Marie‐Paule Lefranc,Isabelle Touitou,Bakridine Mmadi Mrenda,Cécilia Benedito,Étienne Pardoux,Anne-Laure Gagez,Yves‐Marie Pers,Christian Jørgensen,Touhami Mahjoub,Florence Apparailly	2017	9
9	B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation Genetics in Medicine ·Kévin Yauy,Frédéric Tran Mau‐Them,Marjolaine Willems,Christine Coubes,Patricia Blanchet,Christian Herlin,Ikram Taleb Arrada,Elodie Sanchez,Jean-Michel Faure,Marie-Pascale Le Gac,O. Prodhomme,Anne Boland,Vincent Meyer,Jean‐Baptiste Rivière,Yannis Duffourd,Jean‐François Deleuze,Thomas Guignard,Guillaume Captier,Mouna Barat‐Houari,David Geneviève	2017	21
10	Confirmation of TENM3 involvement in autosomal recessive colobomatous microphthalmia American Journal of Medical Genetics Part A ·Nicolas Chassaing,Nicola Ragge,Julie Plaisancié,O. Patat,David Geneviève,François Rivier,Claudie Malrieu‐Eliaou,Christian Hamel,Josseline Kaplan,Patrick Calvas	2016	25
11	Identification of disrupted AUTS2 and EPHA6 genes by array painting in a patient carrying a de novo balanced translocation t(3;7) with intellectual disability and neurodevelopment disorder American Journal of Medical Genetics Part A ·Anouck Schneider,Jacques Puechberty,Bee Ling Ng,Christine Coubes,Vincent Gâtinois,Magali Tournaire,Manon Girard,Bruno Dumont,Pauline Bouret,Julia Magnetto,Amaria Baghdadli,Franck Pellestor,David Geneviève	2015	8
12	Chromothripsis: potential origin in gametogenesis and preimplantation cell divisions. A review Fertility and Sterility ·Franck Pellestor,Vincent Gâtinois,Jacques Puechberty,David Geneviève,Geneviève Lefort	2014	49
13	CEP57 mutation in a girl with mosaic variegated aneuploidy syndrome American Journal of Medical Genetics Part A ·Lucile Pinson,Linda Mannini,Marjolaine Willems,Francesco Cucco,Nicolas Sirvent,Thierry Frébourg,Valentina Quarantotti,Corinne Collet,Anouck Schneider,Pierre Sarda,David Geneviève,Jacques Puechberty,Geneviève Lefort,Antonio Musio	2013	20
14	Loss-of-Function Mutations in Euchromatin Histone Methyl Transferase 1 (EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome The American Journal of Human Genetics ·Tjitske Kleefstra,Han G. Brunner,Jeanne Amiel,Astrid Oudakker,Willy M. Nillesen,Alex Magee,David Geneviève,Valérie Cormier‐Daire,Hilde Van Esch,Jean‐Pierre Fryns,Ben C.J. Hamel,Erik A. Sistermans,Bert B.A. de Vries,Hans van Bokhoven	2006	276
15	Gorlin syndrome presenting as prenatal chylothorax in a girl Prenatal Diagnosis ·David Geneviève,R. Walter,Philippe Gorry,M-L Jacquemont,L. Dupic,Valérie Layet,Arnold Münnich,Valérie Cormier‐Daire,Marc Dommergues,Stanislas Lyonnet,Delphine Mitanchez	2005	8
16	Paternal deletion of the GNAS imprinted locus (including Gnasxl) in two girls presenting with severe pre- and post-natal growth retardation and intractable feeding difficulties European Journal of Human Genetics ·David Geneviève,Damien Sanlaville,Laurence Faivre,Marie‐Laure Kottler,Marguerite Jambou,Philippe Gosset,Dinane Boustani-Samara,Graziella Pinto,Catherine Ozilou,Geneviève Abéguilé,Arnold Munnich,Serge Romana,O Raoul,Valérie Cormier‐Daire,Michel Vekemans	2005	61
17	Familial Mediterranean fever among patients from Karabakh and the diagnostic value of MEFV gene analysis in all classically affected populations Arthritis & Rheumatism ·Cécile Cazeneuve,Zaruhi Hovannesyan,David Geneviève,Hasmik Hayrapetyan,Stéphanie Papin,Emmanuelle Girodon‐Boulandet,Brigitte Boissier,Josué Feingold,Karine Atayan,Tamara Sarkisian,Serge Amselem	2003	36
18	A CGH study of 27 patients with CHARGE association Clinical Genetics ·Damien Sanlaville,Serge Romana,J.M. Lapierre,Jeanne Amiel,David Geneviève,Catherine Ozilou,Marc Le Lorc’h,Sophie Brisset,Philippe Gosset,Clarisse Baumann,C Turleau,Stanislas Lyonnet,Michel Vekemans	2002	21
19	Mild phenotype in a 15‐year‐old boy with Pallister–Killian syndrome American Journal of Medical Genetics Part A ·David Geneviève,Valérie Cormier‐Daire,Damien Sanlaville,Laurence Faivre,Philippe Gosset,L. Allart,Monique Picq,Arnold Münnich,Serge Romana,M-C de Blois,Michel Vekemans	2002	30
20	Identification of MEFV-Independent Modifying Genetic Factors for Familial Mediterranean Fever The American Journal of Human Genetics ·Cécile Cazeneuve,Hasmik Ajrapetyan,Stéphanie Papin,Françoise Roudot‐Thoraval,David Geneviève,Elizaveta Mndjoyan,Marina Papazian,Ashot Sarkisian,Ara Babloyan,Brigitte Boissier,Philippe Duquesnoy,Jean‐Claude Kouyoumdjian,Emmanuelle Girodon‐Boulandet,Gilles Grateau,Tamara Sarkisian,Serge Amselem	2000	155

About David Geneviève

David Geneviève is a scholar working on Genetics, Genetics and Immunology and Allergy, having authored 80 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Genomics and Rare Diseases (13 papers), Genetics and Neurodevelopmental Disorders (9 papers), Connective tissue disorders research (8 papers), Prenatal Screening and Diagnostics (6 papers), Congenital Ear and Nasal Anomalies (5 papers), Fetal and Pediatric Neurological Disorders (5 papers) and Genetic Syndromes and Imprinting (4 papers). The work is most often cited by research in Genetics (1.1k citations), Molecular Biology (1.3k citations) and Genetics (168 citations). David Geneviève has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Valérie Cormier‐Daire, Jeanne Amiel, Arnold Münnich, Stanislas Lyonnet, Vincent Gâtinois, Damien Sanlaville, Michel Vekemans, Loïc de Pontual, Jean‐Pierre Fryns and Willy M. Nillesen. Their work appears in journals such as Nature Genetics, Journal of Clinical Oncology and Blood.

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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