Jacques Puechberty

2.3k total citations
43 papers, 729 citations indexed

About

Jacques Puechberty is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, Jacques Puechberty has authored 43 papers receiving a total of 729 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 22 papers in Plant Science and 18 papers in Molecular Biology. Recurrent topics in Jacques Puechberty's work include Genomic variations and chromosomal abnormalities (24 papers), Chromosomal and Genetic Variations (22 papers) and Prenatal Screening and Diagnostics (14 papers). Jacques Puechberty is often cited by papers focused on Genomic variations and chromosomal abnormalities (24 papers), Chromosomal and Genetic Variations (22 papers) and Prenatal Screening and Diagnostics (14 papers). Jacques Puechberty collaborates with scholars based in France, Germany and Iran. Jacques Puechberty's co-authors include Franck Pellestor, Geneviève Lefort, Gérard Roizès, G. Lefort, Thomas Liehr, P. Sardá, Vincent Gâtinois, T. Anahory, B. Hédon and Pierre Sarda and has published in prestigious journals such as Human Reproduction, Fertility and Sterility and Human Reproduction Update.

In The Last Decade

Jacques Puechberty

41 papers receiving 711 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jacques Puechberty France 17 458 355 311 221 50 43 729
Elke Back Germany 15 576 1.3× 456 1.3× 247 0.8× 138 0.6× 25 0.5× 36 829
Chansonette Harvard Canada 17 417 0.9× 294 0.8× 85 0.3× 185 0.8× 45 0.9× 19 681
Maxine J. Sutcliffe United States 13 375 0.8× 316 0.9× 129 0.4× 130 0.6× 136 2.7× 27 676
Carolina Sismani Cyprus 19 735 1.6× 515 1.5× 184 0.6× 266 1.2× 29 0.6× 75 984
Danuta Galetzka Germany 13 229 0.5× 445 1.3× 91 0.3× 130 0.6× 53 1.1× 39 626
Azzedine Aboura France 17 525 1.1× 311 0.9× 110 0.4× 258 1.2× 100 2.0× 40 767
Herman E. Wyandt United States 15 359 0.8× 205 0.6× 108 0.3× 169 0.8× 17 0.3× 40 517
Ercole Rao Germany 12 777 1.7× 763 2.1× 178 0.6× 46 0.2× 24 0.5× 19 1.1k
Sandra Monfort Spain 13 364 0.8× 264 0.7× 50 0.2× 94 0.4× 39 0.8× 41 530
Zhenhai Du China 11 328 0.7× 1.5k 4.3× 337 1.1× 170 0.8× 180 3.6× 15 1.7k

Countries citing papers authored by Jacques Puechberty

Since Specialization
Citations

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

Fields of papers citing papers by Jacques Puechberty

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacques Puechberty

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

All Works

20 of 20 papers shown
1.
Schneider, Anouck, Marie‐Claire Vincent, Christine Coubes, et al.. (2024). Confined placental mosaicism is a diagnostic pitfall in dystrophinopathies: a clinical report. European Journal of Human Genetics. 34(1). 161–164.
2.
Ranisavljevic, Noémie, et al.. (2021). Whole-genome analysis of a putative rare and complex interchromosomal reciprocal insertion: thorough investigations for a straightforward interpretation. Reproductive BioMedicine Online. 44(4). 636–640. 1 indexed citations
3.
Gâtinois, Vincent, Nicole Bigi, E. Mousty, et al.. (2019). Mosaic complete tetrasomy 21 in a fetus with complete atrioventricular septal defect and minor morphological variations. Molecular Genetics & Genomic Medicine. 7(11). e00895–e00895.
4.
Busa, Tiffany, Dominique P. Germain, Gwenaël Nadeau, et al.. (2017). The role of CNVs in the etiology of rare autosomal recessive disorders: the example of TRAPPC9-associated intellectual disability. European Journal of Human Genetics. 26(1). 143–148. 22 indexed citations
5.
Guissart, Claire, Caroline Raynal, Anne Girardet, et al.. (2016). Non-invasive prenatal diagnosis (NIPD) of cystic fibrosis: an optimized protocol using MEMO fluorescent PCR to detect the p.Phe508del mutation. Journal of Cystic Fibrosis. 16(2). 198–206. 12 indexed citations
6.
Schneider, Anouck, Jacques Puechberty, Bee Ling Ng, et al.. (2015). 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. 167(12). 3031–3037. 8 indexed citations
7.
Pellestor, Franck, Vincent Gâtinois, Jacques Puechberty, David Geneviève, & Geneviève Lefort. (2014). Chromothripsis: potential origin in gametogenesis and preimplantation cell divisions. A review. Fertility and Sterility. 102(6). 1785–1796. 49 indexed citations
8.
Gâtinois, Vincent, Jacques Puechberty, Geneviève Lefort, David Geneviève, & Franck Pellestor. (2014). Les remaniements chromosomiques complexes. médecine/sciences. 30(1). 55–63. 2 indexed citations
9.
Kluger, Nicolas, et al.. (2014). Congenital Linear Streaks on the Face and Neck and Microphthalmia in an Infant Girl. Acta Dermato Venereologica. 94(3). 342–343. 3 indexed citations
10.
Pinson, Lucile, Linda Mannini, Marjolaine Willems, et al.. (2013). CEP57 mutation in a girl with mosaic variegated aneuploidy syndrome. American Journal of Medical Genetics Part A. 164(1). 177–181. 20 indexed citations
11.
Bhatt, Samarth, Marina Manvelyan, Kamran Moradkhani, et al.. (2013). Inverted Segment Size and the Presence of Recombination Hot Spot Clusters Matter in Sperm Segregation Analysis. Cytogenetic and Genome Research. 142(2). 145–149. 6 indexed citations
12.
Vincent, Marie, Corinne Collet, Alain Verloès, et al.. (2013). Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability. European Journal of Human Genetics. 22(1). 52–56. 15 indexed citations
13.
Pellestor, Franck, Jacques Puechberty, Anja Weise, et al.. (2011). Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier. Fertility and Sterility. 95(7). 2433.e17–2433.e22. 31 indexed citations
14.
15.
16.
Pellestor, Franck, B. Andréo, Jacques Puechberty, Geneviève Lefort, & Pierre Sarda. (2006). Analysis of Sperm Aneuploidy by PRINS. Humana Press eBooks. 334. 49–60. 7 indexed citations
17.
Moradkhani, Kamran, Jacques Puechberty, Samarth Bhatt, et al.. (2006). Meiotic segregation of rare Robertsonian translocations: sperm analysis of three t(14q;22q) cases. Human Reproduction. 21(5). 1166–1171. 19 indexed citations
18.
Puechberty, Jacques, et al.. (1999). Hypothesis: For the Worst and for the Best, L1Hs Retrotransposons Actively Participate in the Evolution of the Human Centromeric Alphoid Sequences. Chromosome Research. 7(4). 305–317. 21 indexed citations
19.
Puechberty, Jacques, Sylvie Gimenez, Alain Billault, et al.. (1999). Genetic and Physical Analyses of the Centromeric and Pericentromeric Regions of Human Chromosome 5: Recombination across 5cen. Genomics. 56(3). 274–287. 40 indexed citations
20.
Puechberty, Jacques, et al.. (1998). Informative Genetic Polymorphic Markers within the Centromeric Regions of Human Chromosomes 17 (D17S2205) and 11 (D11S4975). Genomics. 52(2). 166–172. 5 indexed citations

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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