P. Sardá

2.1k total citations
48 papers, 921 citations indexed

About

P. Sardá is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, P. Sardá has authored 48 papers receiving a total of 921 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 12 papers in Molecular Biology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in P. Sardá's work include Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (10 papers) and Chromosomal and Genetic Variations (9 papers). P. Sardá is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (10 papers) and Chromosomal and Genetic Variations (9 papers). P. Sardá collaborates with scholars based in France, Germany and Iran. P. Sardá's co-authors include G. Lefort, B. Hédon, Franck Pellestor, Jacques Puechberty, T. Anahory, Thomas Liehr, D Rieu, F. Mendy, B. Descomps and C. Humeau and has published in prestigious journals such as PEDIATRICS, Journal of Cell Science and The American Journal of Human Genetics.

In The Last Decade

P. Sardá

47 papers receiving 869 citations

Peers

Countries citing papers authored by P. Sardá

Since Specialization

Citations

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

Fields of papers citing papers by P. Sardá

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. Sardá

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	TBL1XR1 mutations in Pierpont syndrome are not restricted to the recurrent p.Tyr446Cys mutation 2018 ·American Journal of Medical Genetics Part A ·(unknown), Julien Thévenon, Yannis Duffourd, Sophie Nambot, (unknown), (unknown), David Geneviève, P. Sardá, (unknown), Paul Kuentz, Constance Wells, Laurence Faivre, Marjolaine Willems	12
2	Inverted Segment Size and the Presence of Recombination Hot Spot Clusters Matter in Sperm Segregation Analysis 2013 ·Cytogenetic and Genome Research ·Samarth Bhatt, Marina Manvelyan, Kamran Moradkhani, (unknown), Kristin Mrasek, Jacques Puechberty, G. Lefort, P. Sardá, Anja Weise, Thomas Liehr, Franck Pellestor	6
3	Syndromes génétiques mimant les infections congénitales : à propos de 2 cas 2011 ·Archives de Pédiatrie ·Marie‐Pier Thibault, (unknown), Elisabeth Tournier‐Lasserve, Yanick J. Crow, François Rivier, Bernard Échenne, (unknown), (unknown), P. Sardá, Agathe Roubertie	2
4	The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated males 2010 ·Clinical Genetics ·David Germanaud, Massimiliano Rossi, Gérald Bussy, Daniel Gérard, Lucie Hertz‐Pannier, Patricia Blanchet, Hélène Dollfus, Fabienne Giuliano, (unknown), P. Sardá, Sabine Sigaudy, Aurore Curie, (unknown), Renaud Touraine, V. des Portes	36
5	Mutations in Cytokine Receptor-Like Factor 1 (CRLF1) Account for Both Crisponi and Cold-Induced Sweating Syndromes 2007 ·The American Journal of Human Genetics ·Nathalie Dagoneau, Samuel Bellais, Patricia Blanchet, P. Sardá, L.I. Al-Gazali, Maja Di Rocco, Céline Huber, Fatima Djouadi, Carine Le Goff, Arnold Münnich, Valérie Cormier‐Daire	51
6	Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm 2007 ·Molecular Human Reproduction ·Samarth Bhatt, Kamran Moradkhani, Kristin Mrasek, Jacques Puechberty, G. Lefort, J. Lespinasse, P. Sardá, Thomas Liehr, S. Hamamah, Franck Pellestor	15
7	Meiotic segregation of rare Robertsonian translocations: sperm analysis of three t(14q;22q) cases 2006 ·Human Reproduction ·Kamran Moradkhani, Jacques Puechberty, Samarth Bhatt, Philippe Vago, L. Janny, G. Lefort, S. Hamamah, P. Sardá, Franck Pellestor	19
8	Rare Robertsonian translocations and meiotic behaviour: sperm FISH analysis of t(13;15) and t(14;15) translocations: A Case Report 2006 ·Human Reproduction ·Kamran Moradkhani, Jacques Puechberty, Samarth Bhatt, J. Lespinasse, Philippe Vago, G. Lefort, P. Sardá, S. Hamamah, Franck Pellestor	26
9	Sperm segregation analysis of a (13;22) Robertsonian translocation carrier by FISH: a comparison of locus-specific probe and whole chromosome painting 2005 ·Human Reproduction ·T. Anahory, S. Hamamah, B. Andréo, B. Hédon, Mireille Claustres, P. Sardá, Franck Pellestor	39
10	Alpha linolenic acid in cholesterol esters: a marker of alphalinolenic acid intake in newborns 2000 ·European Journal of Clinical Nutrition ·(unknown), A. Rodríguez, P. Sardá, (unknown), F. Mendy, B. Descomps	12
11	Longitudinal Multicentric Study of Plasma and Red Blood Cell Fatty Acids and Lipids in Preterm Newborns Fed Human Milk 1999 ·Neonatology ·(unknown), P. Sardá, Dominique Bouglé, Claude Billeaud, (unknown), Nicole Combe, A. Nouvelot, B. Descomps, B. Entressangles, A. Crastes de Paulet, F. Mendy	1
12	Clinical profile of multiple sclerosis in Bengal. 1999 ·PubMed ·(unknown), (unknown), P. Sardá, (unknown), Prasanta Kumar Gangopadhyay, T Roy, (unknown)	27
13	Pallister-Killian syndrome [i(12p)]: first pre-natal diagnosis using cordocentesis in the second trimester confirmed by in situ hybridization 1998 ·Clinical Genetics ·Jean Chiésa, M. Hoffet, (unknown), (unknown), P. Sardá, P. Marès, (unknown)	25
14	Pallister—Killian syndrome [i(12p)]: first pre‐natal diagnosis using cordocentesis in the second trimester confirmed by in situ hybridization 1998 ·Clinical Genetics ·Jean Chiésa, M. Hoffet, (unknown), (unknown), P. Sardá, P. Marès, (unknown)	10
15	Effects of preterm infant formula supplementation with α-linolenic acid with a linoleate/α-linolenate ratio of 6: a multicentric study 1997 ·European Journal of Clinical Nutrition ·Claude Billeaud, Dominique Bouglé, P. Sardá, Nicole Combe, (unknown), (unknown), B. Entressangles, B. Descomps, A. Nouvelot, F. Mendy	22
16	Interstitial deletion of chromosome 1 del (1) (q32 q42): case report and review of the literature 1992 ·Clinical Genetics ·P. Sardá, G. Lefort, Sylvie Taviaux, C. Humeau, D Rieu	2
17	Favourable outcome in 33 triplet pregnancies managed between 1985–1990 1992 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·P. Boulot, B. Hédon, (unknown), P. Sardá, F. Montoya, P. Marès, C. Humeau, (unknown), F Laffargue, (unknown)	26
18	Epidemiology of diaphragmatic hernia in Languedoc-Roussillon. 1991 ·PubMed ·P. Sardá, Pierre Devaux, G. Lefort, C. Humeau, D Rieu	6
19	[Limitations of prenatal treatment of congenital toxoplasmosis with a sulfadiazine-pyrimethamine combination]. 1990 ·PubMed ·P. Boulot, Francine Pratlong, P. Sardá, (unknown), B. Hédon, F Laffargue, (unknown)	7
20	Reductions par le zinc en presence d'acides—II 1975 ·Tetrahedron ·(unknown), P. Sardá	5

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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