G Malpuech

1.3k total citations
68 papers, 830 citations indexed

About

G Malpuech is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, G Malpuech has authored 68 papers receiving a total of 830 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 19 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in G Malpuech's work include Sexual Differentiation and Disorders (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). G Malpuech is often cited by papers focused on Sexual Differentiation and Disorders (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). G Malpuech collaborates with scholars based in France, Canada and Netherlands. G Malpuech's co-authors include P Vanlieferinghen, F Deméocq, Christine Francannet, Jean‐Bernard Palcoux, Pierre Déchelotte, Anne-Marie Pulichino, Sophie Vallette-Kasic, J. Kanold, Monique De Vroede and Thierry Brue and has published in prestigious journals such as Genes & Development, Cancer and Journal of Clinical Microbiology.

In The Last Decade

G Malpuech

64 papers receiving 798 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G Malpuech France 18 321 304 166 95 93 68 830
Gen Isshiki Japan 19 164 0.5× 267 0.9× 116 0.7× 24 0.3× 79 0.8× 70 858
Ruben van ‘t Slot Netherlands 20 580 1.8× 569 1.9× 38 0.2× 29 0.3× 163 1.8× 29 1.5k
J.M. Garnier France 14 337 1.0× 481 1.6× 67 0.4× 39 0.4× 58 0.6× 41 964
Dolores López Spain 20 68 0.2× 189 0.6× 47 0.3× 21 0.2× 83 0.9× 43 881
Melanie Scully United States 12 123 0.4× 387 1.3× 40 0.2× 23 0.2× 136 1.5× 14 1.1k
Ingrid E. Gienapp United States 19 164 0.5× 208 0.7× 39 0.2× 26 0.3× 87 0.9× 31 1.5k
Rachel A. Brown United States 15 72 0.2× 219 0.7× 34 0.2× 133 1.4× 140 1.5× 26 856
H Yabuuchi Japan 18 77 0.2× 201 0.7× 113 0.7× 16 0.2× 65 0.7× 55 805
Bach Jf France 15 96 0.3× 111 0.4× 84 0.5× 60 0.6× 151 1.6× 93 785
G Bendixen Denmark 18 286 0.9× 85 0.3× 192 1.2× 53 0.6× 210 2.3× 51 1.1k

Countries citing papers authored by G Malpuech

Since Specialization
Citations

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

Fields of papers citing papers by G Malpuech

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G Malpuech

This figure shows the co-authorship network connecting the top 25 collaborators of G Malpuech. A scholar is included among the top collaborators of G Malpuech 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 G Malpuech. G Malpuech 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.
Pélissier, Philippe, Étienne Merlin, Fabienne Prieur, et al.. (2005). Hypoplasie congénitale des surrénales : à propos de quatre observations. Archives de Pédiatrie. 12(4). 380–384. 9 indexed citations
2.
Palcoux, Jean‐Bernard, Martine De Meyer, P Jouanel, P Vanlieferinghen, & G Malpuech. (2002). Comparison of Different Treatment Regimens in a Case of Homozygous Familial Hypercholesterolemia. Therapeutic Apheresis. 6(2). 136–139. 7 indexed citations
3.
Bernard-Gallon, Dominique, et al.. (2000). BRCA1 and BRCA2 protein expressions in an ovotestis of a 46, XX true hermaphrodite. Breast Cancer Research. 3(1). 61–5. 1 indexed citations
4.
Paillard, Catherine, J. Kanold, Karima Yakouben, et al.. (2000). Two‐step immunoablative treatment with autologous peripheral blood CD34+ cell transplantation in an 8‐year‐old boy with autoimmune haemolytic anaemia. British Journal of Haematology. 110(4). 900–902. 6 indexed citations
5.
Chambon, M., Jean‐Luc Bailly, Cécile Henquell, et al.. (1999). An outbreak due to Echovirus type 30 in a neonatal unit in France in 1997: usefulness of PCR diagnosis. Journal of Hospital Infection. 43(1). 63–68. 25 indexed citations
6.
Raynaud, Martine, et al.. (1998). X‐linked mental retardation with isolated growth hormone deficiency is mapped to Xq22–Xq27.2 in one family. American Journal of Medical Genetics. 76(3). 255–261. 2 indexed citations
7.
Kanold, Justyna, Pascale Halle, Chantal Rapatel, et al.. (1998). Safe and Efficient Peripheral Blood Stem Cell Collection in the Smallest of Children. Therapeutic Apheresis. 2(1). 49–57. 18 indexed citations
8.
Cossée, Mireille, Céline Moutou, Valérie Biancalana, et al.. (1997). Le syndrome X fragile est encore méconnu: efficacité du diagnostic moléculaire chez les proposants avec retard mental. Archives de Pédiatrie. 4(3). 227–236. 1 indexed citations
9.
Kanold, J., Marc Berger, J Chassagne, et al.. (1994). Use of G‐CSF alone to mobilize peripheral blood stem cells for collection from children. British Journal of Haematology. 88(3). 633–635. 28 indexed citations
10.
Philippe, Christophe, et al.. (1994). Hypomagensemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint. Human Genetics. 93(5). 587–91. 21 indexed citations
11.
Malpuech, G, et al.. (1993). [Discovery, in neonatal screening, of 2 families carrying a syndrome of generalized resistance to thyroid hormones].. PubMed. 40(7). 396–403.
12.
Palcoux, Jean‐Bernard, Martine De Meyer, P Jouanel, et al.. (1993). Treatment of homozygous familial hypercholesterolemia by plasma exchange and LDL-apheresis. Transfusion Science. 14(4). 423–427. 3 indexed citations
13.
Labbé, Antoine, Pierre Déchelotte, Didier Lémery, & G Malpuech. (1992). Pulmonary hyperplasia in Fraser syndrome. Pediatric Pulmonology. 14(2). 131–134. 5 indexed citations
14.
Francannet, Christine, et al.. (1990). Fraser syndrome with renal agenesis in two consanguineous Turkish families. American Journal of Medical Genetics. 36(4). 477–479. 18 indexed citations
15.
Vanlieferinghen, P, et al.. (1987). [Congenital stenosis of the aqueduct of Sylvius transmitted in an autosomal recessive mode (5 cases in 2 families)].. PubMed. 35(4). 251–8. 6 indexed citations
16.
Malpuech, G, F Deméocq, Jean‐Bernard Palcoux, P Vanlieferinghen, & John M. Opitz. (1983). A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies. American Journal of Medical Genetics. 16(4). 475–480. 38 indexed citations
17.
Deméocq, F, et al.. (1980). [Association of Fanconi's anemia and growth hormone deficiency].. PubMed. 35(6). 527–32.
18.
Malpuech, G, et al.. (1976). Bilan d'une consultation d'enfants deficients auditifs au cours des trois dernieres annees: aspects génétiques. 199–206. 1 indexed citations
19.
Raynaud, Emmanuel, et al.. (1971). Ictère retentionnel néonatal revelateur de la mucoviscidose. 28(3). 210–233. 1 indexed citations
20.
Malpuech, G, et al.. (1971). Délétion complète du bras court du chromosome 18 et translocation G-18 avec dyschromie et hypothyroidie.. 28(8). 3 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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