Nicolas Gruchy

1.5k total citations
31 papers, 572 citations indexed

About

Nicolas Gruchy is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Nicolas Gruchy has authored 31 papers receiving a total of 572 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 19 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Nicolas Gruchy's work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (7 papers) and Genetic Syndromes and Imprinting (5 papers). Nicolas Gruchy is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (7 papers) and Genetic Syndromes and Imprinting (5 papers). Nicolas Gruchy collaborates with scholars based in France, Japan and United Kingdom. Nicolas Gruchy's co-authors include Nathalie Leporrier, Hervé Mittre, Nicolas Richard, Marie‐Laure Kottler, Philippe Galéra, Marie‐France Portnoï, Nadia Coudray, Joris Andrieux, Florence Legendre and Sandrine Marlin and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Nicolas Gruchy

29 papers receiving 539 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nicolas Gruchy France 15 328 285 137 75 69 31 572
Rita Fischetto Italy 15 538 1.6× 486 1.7× 219 1.6× 27 0.4× 61 0.9× 33 837
Yolande van Bever Netherlands 18 441 1.3× 297 1.0× 191 1.4× 56 0.7× 218 3.2× 46 871
A. David France 13 230 0.7× 326 1.1× 64 0.5× 42 0.6× 115 1.7× 42 579
R M Winter United Kingdom 14 402 1.2× 276 1.0× 94 0.7× 26 0.3× 165 2.4× 32 683
Koh‐ichiro Yoshiura Japan 14 170 0.5× 181 0.6× 185 1.4× 37 0.5× 58 0.8× 35 549
Kenneth McElreavey France 12 221 0.7× 309 1.1× 62 0.5× 38 0.5× 101 1.5× 30 555
Luciani R. Carvalho Brazil 17 409 1.2× 486 1.7× 75 0.5× 13 0.2× 116 1.7× 52 1.0k
Azzedine Aboura France 17 525 1.6× 311 1.1× 258 1.9× 18 0.2× 41 0.6× 40 767
Ying‐Xia Cui China 15 264 0.8× 256 0.9× 46 0.3× 49 0.7× 47 0.7× 68 533
Norma Leonard Canada 14 103 0.3× 279 1.0× 68 0.5× 28 0.4× 78 1.1× 30 520

Countries citing papers authored by Nicolas Gruchy

Since Specialization
Citations

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

Fields of papers citing papers by Nicolas Gruchy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicolas Gruchy

This figure shows the co-authorship network connecting the top 25 collaborators of Nicolas Gruchy. A scholar is included among the top collaborators of Nicolas Gruchy 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 Nicolas Gruchy. Nicolas Gruchy 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.
Colson, Cindy, et al.. (2023). Phenotypic and genotypic characterization of 1q21.1 copy number variants: A report of 34 new individuals and literature review. American Journal of Medical Genetics Part A. 194(3). e63457–e63457. 6 indexed citations
2.
Kishikawa, Shotaro, Vijay Gupta, Natalia T. Leach, et al.. (2023). A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome. Scientific Reports. 13(1). 12984–12984. 2 indexed citations
3.
Benmoussa, Abderrahim, Émilie Brotin, Françoise Rédiní, et al.. (2023). MiR-4270 acts as a tumor suppressor by directly targeting Bcl-xL in human osteosarcoma cells. Frontiers in Oncology. 13. 1220459–1220459. 1 indexed citations
4.
5.
Socha, Magdalena, Anna Sowińska‐Seidler, Uirá Souto Melo, et al.. (2021). Position effects at the FGF8 locus are associated with femoral hypoplasia. The American Journal of Human Genetics. 108(9). 1725–1734. 7 indexed citations
6.
Bieth, Éric, Juliette Nectoux, Anne Girardet, et al.. (2020). Genetic counseling for cystic fibrosis: A basic model with new challenges. Archives de Pédiatrie. 27. eS30–eS34. 5 indexed citations
7.
Colson, Cindy, Matthieu Décamp, Nicolas Gruchy, et al.. (2019). High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B. Bone. 123. 145–152. 18 indexed citations
8.
Legendre, Florence, David Ollitrault, Tangni Gómez-Leduc, et al.. (2017). Enhanced chondrogenesis of bone marrow-derived stem cells by using a combinatory cell therapy strategy with BMP-2/TGF-β1, hypoxia, and COL1A1/HtrA1 siRNAs. Scientific Reports. 7(1). 3406–3406. 38 indexed citations
9.
Gómez-Leduc, Tangni, Magalie Hervieu, Florence Legendre, et al.. (2016). Chondrogenic commitment of human umbilical cord blood-derived mesenchymal stem cells in collagen matrices for cartilage engineering. Scientific Reports. 6(1). 32786–32786. 38 indexed citations
10.
Gruchy, Nicolas, et al.. (2016). Immunoanalytical characteristics of unconjugated estriol: indications and analytical performances. Annales de biologie clinique. 74(6). 717–723.
11.
Gruchy, Nicolas, Nicolas Bigot, Corinne Pasquier, et al.. (2014). Involvement and alteration of the Sonic Hedgehog pathway is associated with decreased cholesterol level in trisomy 18 and SLO amniocytes. Molecular Genetics and Metabolism. 112(2). 177–182. 6 indexed citations
12.
Molin, Arnaud, G. Benoist, Corinne Jeanne‐Pasquier, et al.. (2013). 12q21 Microdeletion in a fetus with Meckel syndrome involving CEP290/MKS4. European Journal of Medical Genetics. 56(10). 580–583. 11 indexed citations
13.
Richard, Nicolas, Nadia Coudray, Hervé Mittre, et al.. (2012). A New Deletion Ablating NESP55 Causes Loss of Maternal Imprint of A/BGNASand Autosomal Dominant Pseudohypoparathyroidism Type Ib. The Journal of Clinical Endocrinology & Metabolism. 97(5). E863–E867. 71 indexed citations
14.
Gruchy, Nicolas, Matthieu Décamp, Nicolas Richard, et al.. (2011). Array CGH analysis in high‐risk pregnancies: comparing DNA from cultured cells and cell‐free fetal DNA. Prenatal Diagnosis. 32(4). 383–388. 29 indexed citations
15.
Devillard, Françoise, Vincent Guinchat, Daniel Moreno‐De‐Luca, et al.. (2010). Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism. American Journal of Medical Genetics Part A. 152A(9). 2346–2354. 14 indexed citations
16.
17.
Gruchy, Nicolas, Marine Lebrun, M. Herlicoviez, et al.. (2008). Supernumerary marker chromosomes management in prenatal diagnosis. American Journal of Medical Genetics Part A. 146A(21). 2770–2776. 23 indexed citations
18.
Gruchy, Nicolas, Marie‐Line Jacquemont, Stanislas Lyonnet, et al.. (2007). Recurrent inverted duplication of 2p with terminal deletion in a patient with the classical phenotype of trisomy 2p23‐pter. American Journal of Medical Genetics Part A. 143A(20). 2417–2422. 16 indexed citations
19.
Portnoï, Marie‐France, Nicolas Gruchy, Sandrine Marlin, et al.. (2007). Midline defects in deletion 18p syndrome: clinical and molecular characterization of three patients. Clinical Dysmorphology. 16(4). 247–252. 34 indexed citations
20.
Portnoï, Marie‐France, Nicolas Gruchy, Valérie Malan, et al.. (2005). 22q11.2 duplication syndrome: Two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes. American Journal of Medical Genetics Part A. 137A(1). 47–51. 74 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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