David Geneviève

682 total citations
7 papers, 318 citations indexed

About

David Geneviève is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, David Geneviève has authored 7 papers receiving a total of 318 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 1 paper in Surgery. Recurrent topics in David Geneviève's work include Craniofacial Disorders and Treatments (2 papers), Cleft Lip and Palate Research (2 papers) and Organ and Tissue Transplantation Research (1 paper). David Geneviève is often cited by papers focused on Craniofacial Disorders and Treatments (2 papers), Cleft Lip and Palate Research (2 papers) and Organ and Tissue Transplantation Research (1 paper). David Geneviève collaborates with scholars based in France, Netherlands and Germany. David Geneviève's co-authors include Alain Verloès, Martine Le Merrer, Nicole Laurent, Ton van Essen, Rafaëlle Bernard, Annachiara De Sandre‐Giovannoli, Caroline Gaudy‐Marqueste, S. Hadj‐Rabia, Pierre Cau and Claire Navarro and has published in prestigious journals such as Nucleic Acids Research, Human Molecular Genetics and Plastic & Reconstructive Surgery.

In The Last Decade

David Geneviève

6 papers receiving 311 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 of co-authors of David Geneviève

This figure shows the co-authorship network connecting the top 25 collaborators of David Geneviève. A scholar is included among the top collaborators of David Geneviève 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 David Geneviève. David Geneviève is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Disrupted transcriptional networks regulated by CHD1L during neurodevelopment underlie the mirrored neuroanatomical and growth phenotypes of the 1q21.1 copy number variant 2025 ·Nucleic Acids Research ·(unknown), Maria Nicla Loviglio, Ye Tao, Peggy Tilly, Céline Keime, C. R. Weber, (unknown), (unknown), Bastien Morlet, Olivia Wendling, Hugues Jacobs, (unknown), David Geneviève, Juliette D. Godin, Christophe Romier, Delphine Duteil, Christelle Golzio	0
2	Mandibular‐pelvic‐patellar syndrome is a novel PITX1‐related disorder due to alteration of PITX1 transactivation ability 2020 ·Human Mutation ·(unknown), (unknown), (unknown), (unknown), Gaëtan Lesca, Nicolas Chatron, Audrey Labalme, Damien Sanlaville, Patrick Edery, Julien Thévenon, Laurence Faivre, (unknown), O. Prodhomme, Fabienne Escande, Sylvie Manouvrier, Florence Petit, David Geneviève, Massimiliano Rossi	4
3	Treacher Collins Syndrome: A Systematic Review of Evidence-Based Treatment and Recommendations 2016 ·Plastic & Reconstructive Surgery ·Christian Herlin, David Geneviève, Marie Vincent, B. Chaput, Guillaume Captier	3
4	Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability 2013 ·European Journal of Human Genetics ·Marie Vincent, Corinne Collet, Alain Verloès, Laëtitia Lambert, Christian Herlin, Catherine Blanchet, Elodie Sanchez, Séverine Drunat, Jacqueline Vigneron, Jean Laplanche, Jacques Puechberty, Pierre Sarda, David Geneviève	15
5	Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia 2011 ·European Journal of Human Genetics ·(unknown), (unknown), Valérie Malan, Patrick Callier, Célia Cretolle, Laurence Faivre, David Geneviève, Alice Goldenberg, Delphine Héron, Sandra Mercier, Nicole Philip, Sabine Sigaudy, Alain Verloès, Sabine Sarnacki, Arnold Münnich, Michel Vekemans, Stanislas Lyonnet, Heather Etchevers, Jeanne Amiel, Loïc de Pontual	23
6	Exclusion of the dymeclin and PAPSS2 genes in a novel form of spondyloepimetaphyseal dysplasia and mental retardation 2005 ·European Journal of Human Genetics ·David Geneviève, Delphine Héron, Vincent El Ghouzzi, C. Prost‐Squarcioni, Martine Le Merrer, Aurélia Jacquette, Damien Sanlaville, Florence Pinton, Nathalie Villeneuve, G. Kalifa, Arnold Münnich, Valérie Cormier‐Daire	7
7	Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy 2004 ·Human Molecular Genetics ·Claire Navarro, Annachiara De Sandre‐Giovannoli, Rafaëlle Bernard, Irène Boccaccio, Amandine Boyer, David Geneviève, S. Hadj‐Rabia, Caroline Gaudy‐Marqueste, (unknown), P. Vabres, Laurence Bonhomme‐Faivre, Alain Verloès, Ton van Essen, Elisabeth Flori, Raoul C. M. Hennekam, Frits A. Beemer, Nicole Laurent, Martine Le Merrer, Pierre Cau, Nicolas Lévy	266

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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