Pierre Sarda

5.0k citations

58 papers · 1.7k indexed · h-index 24

Impact in

Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Nutrition and Dietetics top 5%
- Fatty Acid Research and Health

Papers in

Developmental Biology 2
Genetics 21
- Genomic variations and chromosomal abnormalities 11
- Genetic Syndromes and Imprinting 4

Co-authors: B. Descomps Pierre Boulot A. Rodríguez Michel Goossens Geneviève Lefort Frédérique Bonnet‐Brilhault Jacques Puechberty Claude Léger
Journals: European Journal of Human Genetics (6 papers)Prenatal Diagnosis (5 papers)The American Journal of Human Genetics (3 papers)Tetrahedron Letters (3 papers)American Journal of Obstetrics and Gynecology (2 papers)
Partner nations: France United States Germany

In The Last Decade

Pierre Sarda

57 papers receiving 1.6k citations

Peers

Countries citing papers authored by Pierre Sarda

Since Specialization

Citations

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

Fields of papers citing papers by Pierre Sarda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences Journal of Medical Genetics ·Solveig Heide, Sandra Chantot‐Bastaraud, Boris Keren, Madeleine D. Harbison, Salah Azzi, Sylvie Rossignol, Caroline Michot, Onnalin Mancaket, Bénédicte Demeer, Claudine Heinrichs, Ron S. Newfield, Pierre Sarda, Lionel Van Maldergem, Lubka Marinova, Éloïse Giabicani, Jean‐Pierre Siffroi, Yves Le Bouc, Irène Netchine, Frédéric Brioude	2017	34
2	Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary to VPS13B mutations American Journal of Medical Genetics Part A ·Lucie Gueneau, Laurence Duplomb, Pierre Sarda, Christian Hamel, Bernard Aral, Salima El Chehadeh, Nadège Gigot, Judith St‐Onge, Patrick Callier, Julien Thévenon, Frédéric Huet, Virginie Carmignac, Nathalie Droin, Laurence Faivre, Christel Thauvin‐Robinet	2013	11
3	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
4	Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus The American Journal of Human Genetics ·Pierre Cacciagli, Moskau Artèmov, Gian Franco Pagano, Jean‐Christophe Roux, Imen Dorboz, Jean‐Pierre Desvignes, Catherine Badens, Marc Délepine, Mark Lathrop, Pierre Cau, Nicolas Lévy, Nadine Girard, Pierre Sarda, Odile Boespflug‐Tanguy, Laurent Villard	2013	48
5	Heterochromatic Genes Undergo Epigenetic Changes and Escape Silencing in Immunodeficiency, Centromeric Instability, Facial Anomalies (ICF) Syndrome PLoS ONE ·Élise Laforge, Yuemei Lin, Isabelle Rivals, Marie‐Paule Lefranc, Pierre Sarda, Mireille Claustres, André Mégarbané, Albertina De Sario	2011	25
6	Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier Fertility and Sterility ·Franck Pellestor, Jacques Puechberty, Anja Weise, Geneviève Lefort, T. Anahory, Thomas Liehr, Pierre Sarda	2011	31
7	POLG exon 22 skipping induced by different mechanisms in two unrelated cases of Alpers syndrome Mitochondrion ·Bénédicte Mousson de Camaret, E.Wesley Ely, Martine Mayençon, Laura Glitman, Camila Cano Caporale, P. Clerc-Renaud, Isabelle Rouvet, M. T. Zabot, François Rivier, Pierre Sarda, Vincent des Portes, Dominique Bozon	2010	5
8	Bardet-Biedl Syndrome Clinical Journal of the American Society of Nephrology ·浩水本, Vincent Marion, Corinne Stoetzel, M. Durand, Muriel Holder, Sabine Sigaudy, Pierre Sarda, Christian P. Hamel, Christian Brandt, Hélène Dollfus, Bruno Moulin	2010	91
9	Identification of proteomic changes during human liver development by 2D-DIGE and mass spectrometry Journal of Hepatology ·Márcio Nakanishi, José Ramos, Agnès Robert, Daniel Lafitte, Nicole Bigi, Pierre Sarda, Dalila Laoudj‐Chenivesse, Francis Navarro, Pierre Blanc, Eric Assénat, Patrick Maurel, Jean‐Marc Pascussi, Marie‐José Vilarem	2009	9
10	TCF4Deletions in Pitt-Hopkins Syndrome Human Mutation ·Irina Giurgea, Chantal Missirian, Pierre Cacciagli, Sandra Whalen, Tessa Fredriksen, Edmond Lebée, Julia Rankin, Michèle Mathieu‐Dramard, G Morin, Dominique Martin‐Coignard, Christèle Dubourg, B. Chabrol, E Torroella-Menendez-Fortun, Fabienne Giuliano, Mark Matsunagaa, Nicole Philip, Pierre Sarda, Laurent Villard, Michel Goossens, Anne Moncla	2008	45
11	Analysis of Sperm Aneuploidy by PRINS Humana Press eBooks ·Franck Pellestor, B. Andréo, Jacques Puechberty, Geneviève Lefort, Pierre Sarda	2006	7
12	High heterogeneity of CFTR mutations and unexpected low incidence of cystic fibrosis in the Mediterranean France Journal of Cystic Fibrosis ·Marie des Georges, Caroline Guittard, Diana Valdes, C Moura-Netto, Jacques Sarles, Pierre Sarda, Mireille Claustres	2004	21
13	Six novel heterozygous MLH1, MSH2, and MSH6 and one homozygous MLH1 germline mutations in hereditary nonpolyposis colorectal cancer Cancer Genetics and Cytogenetics ·Jean‐Marc Rey, Mehrdad Noruzinia, Jean‐Paul Brouillet, Pierre Sarda, Thierry Maudelondé, Pascal Pujol	2004	20
14	Spectrum of PTCH1 Mutations in French Patients with Gorlin Syndrome Journal of Investigative Dermatology ·智和吉岡, Yves‐Jean Bignon, Valérie Drouin‐Garraud, Pierre Sarda, Michel Longy, Didier Lacombe, Philippe Gorry	2003	75
15	Meier-Gorlin syndrome: Report of eight additional cases and review American Journal of Medical Genetics ·Ernie M.H.F. Bongers, John M. Opitz, Alan Fryer, Pierre Sarda, Raoul C. M. Hennekam, T. Scanlon, Duane Superneau, Cristian Alexander Rocha Álvarez, J. D. Copple, Hans van Bokhoven, Ben C.J. Hamel, Nine V.A.M. Knoers	2001	47
16	Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain The American Journal of Human Genetics ·Renaud Touraine, Tania Attié‐Bitach, E. Manceau, Eckhard Korsch, Pierre Sarda, Véronique Pingault, Férechté Encha‐Razavi, Anna Pelet, Joëlle Augé, A Nivelon‐Chevallier, A. M. Holschneider, Marc Munnes, Oei Kurniawan Utomo, Michel Goossens, Arnold Munnich, 王鹏成, Stanislas Lyonnet	2000	124
17	Expression of FMR1, FXR1, and FXR2 Genes in Human Prenatal Tissues Journal of Neuropathology & Experimental Neurology ·Cendra Agulhon, Patricia Blanchet, Alexandra Kobetz, Dominique Marchant, G.D.B.W. Wanders, Pierre Sarda, Claude Moraine, Annie Sittler, Valérie Biancalana, Alain Malafosse, Marc Abitbol	1999	41
18	Blastogenesis dominant 1: A sequence with midline anomalies and heterotaxy American Journal of Medical Genetics ·Caspar Matzhold, Pierre Sarda, Romano Tenconi, M Ferrière, Patrice Bouvagnet	1997	12
19	Relationships between Red Blood Cell Vitamin E and Polyunsaturated Fatty Acid in the Premature Infant Annals of Nutrition and Metabolism ·Iwara I.A, A. Nouvelot, Claude Billeaud, Pierre Sarda, B. Entressangles, B. Descomps, Alexandros Ioannidis	1996	8
20	The Use of Bioelectrical Impedance Analysis in Newborns. The Need for Standardization PubMed ·Agnès Gartner, Bernard Maire, Francis Delpeuch, Pierre Sarda, 栾曦, D Rieu	1993	7

About Pierre Sarda

Pierre Sarda is a scholar working on Developmental Biology, Genetics, Aging, Biochemistry and Nutrition and Dietetics, having authored 58 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (7 papers), Fatty Acid Research and Health (6 papers), Genetic Syndromes and Imprinting (4 papers), Metabolomics and Mass Spectrometry Studies (4 papers), Carbohydrate Chemistry and Synthesis (4 papers), Hedgehog Signaling Pathway Studies (4 papers) and RNA regulation and disease (4 papers). The work is most often cited by research in Genetics (626 citations), Nutrition and Dietetics (210 citations), Biological Psychiatry (34 citations), Molecular Biology (922 citations) and Sensory Systems (60 citations). Pierre Sarda has collaborated with scholars based in France, United States and Germany. Frequent co-authors include B. Descomps, Pierre Boulot, A. Rodríguez, Michel Goossens, Geneviève Lefort, Frédérique Bonnet‐Brilhault, Jacques Puechberty, Claude Léger, Renaud Touraine and Lydie Nadal‐Desbarats. Their work appears in journals such as European Journal of Human Genetics, Prenatal Diagnosis, The American Journal of Human Genetics, Tetrahedron Letters and American Journal of Obstetrics and Gynecology.

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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