G. Bourrouillou

1.0k total citations
40 papers, 587 citations indexed

About

G. Bourrouillou is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, G. Bourrouillou has authored 40 papers receiving a total of 587 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 10 papers in Pediatrics, Perinatology and Child Health and 10 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in G. Bourrouillou's work include Prenatal Screening and Diagnostics (10 papers), Alkaline Phosphatase Research Studies (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). G. Bourrouillou is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Alkaline Phosphatase Research Studies (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). G. Bourrouillou collaborates with scholars based in France, Belgium and United Kingdom. G. Bourrouillou's co-authors include Nicole Dastugue, P Colombiès, Patrick Calvas, Louis Bujan, M. Rolland, Marc Fellous, Jean Pierre Siffroi, Ken McElreavey, Patrick Calvas and Lluís Quintana‐Murci and has published in prestigious journals such as Human Molecular Genetics, Human Reproduction and British Journal of Haematology.

In The Last Decade

G. Bourrouillou

39 papers receiving 540 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. Bourrouillou France 14 398 279 147 146 95 40 587
Paolo Guanciali Franchi Italy 14 298 0.7× 220 0.8× 98 0.7× 80 0.5× 71 0.7× 31 484
Paolo Guanciali‐Franchi Italy 10 144 0.4× 222 0.8× 71 0.5× 154 1.1× 37 0.4× 24 443
Didier Theophile France 11 413 1.0× 310 1.1× 55 0.4× 127 0.9× 31 0.3× 15 703
Alida C. Knegt Netherlands 14 257 0.6× 271 1.0× 74 0.5× 232 1.6× 37 0.4× 35 652
Tracy N. Hadnott United States 7 507 1.3× 333 1.2× 65 0.4× 107 0.7× 140 1.5× 11 752
Gregor Schlüter Germany 13 186 0.5× 246 0.9× 151 1.0× 37 0.3× 29 0.3× 25 486
Ulrike Mau Germany 8 356 0.9× 349 1.3× 176 1.2× 454 3.1× 25 0.3× 10 777
Daniela Bettio Italy 12 277 0.7× 169 0.6× 39 0.3× 235 1.6× 45 0.5× 35 535
Anahita Mohseni Meybodi Iran 15 250 0.6× 267 1.0× 248 1.7× 67 0.5× 46 0.5× 66 582
Jean‐Louis Taillemite France 12 247 0.6× 193 0.7× 25 0.2× 80 0.5× 98 1.0× 15 368

Countries citing papers authored by G. Bourrouillou

Since Specialization
Citations

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

Fields of papers citing papers by G. Bourrouillou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Bourrouillou

This figure shows the co-authorship network connecting the top 25 collaborators of G. Bourrouillou. A scholar is included among the top collaborators of G. Bourrouillou 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. Bourrouillou. G. Bourrouillou 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.
Plaisancié, Julie, Laurence Bouneau, Claude Cancès, et al.. (2013). Distal 10q monosomy: New evidence for a neurobehavioral condition?. European Journal of Medical Genetics. 57(1). 47–53. 30 indexed citations
2.
Dupé, Valérie, Lucie Rochard, Sandra Mercier, et al.. (2010). NOTCH, a new signaling pathway implicated in holoprosencephaly. Human Molecular Genetics. 20(6). 1122–1131. 37 indexed citations
3.
Édouard, Thomas, C. Prost‐Squarcioni, Yves Dulac, et al.. (2009). Polyvalvular heart disease with joint hypermobility, characteristic facies, and particular skin abnormalities: New cases of “polyvalvular heart disease syndrome” or new association?. European Journal of Medical Genetics. 53(1). 29–34.
4.
Chassaing, Nicolas, P. De Mas, Sophie Julia, et al.. (2004). Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy‐like phenotype. American Journal of Medical Genetics Part A. 128A(4). 410–413. 21 indexed citations
5.
Caignec, Cédric Le, P. De Mas, Marie‐Claire Vincent, et al.. (2004). Subtelomeric 6p deletion: Clinical, FISH, and array CGH characterization of two cases. American Journal of Medical Genetics Part A. 132A(2). 175–180. 32 indexed citations
6.
Farge, F. De La, et al.. (2002). Maternal serum urea resistant alkaline phosphatase in Down syndrome pregnancy. Early Human Development. 67(1-2). 55–59. 5 indexed citations
7.
8.
Siffroi, Jean Pierre, Csilla Krausz, Sandrine Barbaux, et al.. (2000). Sex chromosome mosaicism in males carrying Y chromosome long arm deletions. Human Reproduction. 15(12). 2559–2562. 109 indexed citations
9.
Denier, Colette, et al.. (1999). Expression of a liver/bone–intestinal hybrid of alkaline phosphatase in neutrophils of Down's syndrome patients. Clinica Chimica Acta. 279(1-2). 167–173. 3 indexed citations
10.
Vergnes, Hugues, et al.. (1994). Changes in Immunological Properties of Neutrophil Alkaline Phosphatase in Trisomy 21 Pregnancies. Acta Haematologica. 92(3). 113–118. 2 indexed citations
11.
Bourrouillou, G., et al.. (1993). Biochemical and immunological characteristics of neutrophil alkaline phosphatase in Down's syndrome. Clinica Chimica Acta. 218(1). 105–112. 2 indexed citations
12.
Marguery, M.C., Flavio Giordano, M Parant, et al.. (1993). Fabry’s Disease: Heterozygous Form of Different Expression in Two Monozygous Twin Sisters. Dermatology. 187(1). 9–15. 24 indexed citations
13.
Dastugue, Nicole, Alain Robert, Catherine Payen, et al.. (1992). Prognostic significance of karyotype in a twelve-year follow-up in childhood acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 64(1). 49–55. 11 indexed citations
14.
Bourrouillou, G., Louis Bujan, Patrick Calvas, et al.. (1992). [Role and contribution of karyotyping in male infertility].. PubMed. 2(2). 189–95. 17 indexed citations
15.
Vergnes, Hugues, R Biermé, G. Bourrouillou, et al.. (1991). Difference in activity properties and subcellular distribution of neutrophil alkaline phosphatase between normal individuals and patients with trisomy 21. British Journal of Haematology. 77(3). 282–286. 3 indexed citations
16.
Dastugue, Nicole, Cécile Demur, R. Bugat, et al.. (1988). Association of the Philadelphia chromosome and 5q− in secondary blood disorder. Cancer Genetics and Cytogenetics. 30(2). 253–259. 13 indexed citations
17.
Vergnes, Hugues, et al.. (1988). An Enzymatic Marker in Mothers of Trisomy 21 Children:Neutrophil Alkaline Phosphatase. Enzyme. 39(3). 174–180. 6 indexed citations
18.
Vergnes, Hugues, et al.. (1988). Heat resistance, immunological and quantitative changes of neutrophil alkaline phosphatase in trisomy 21 pregnancies. Human Genetics. 78(3). 240–243. 5 indexed citations
19.
Arnaud, M. B., G. Bourrouillou, M. Rolland, et al.. (1984). [Trisomy 12(pter----q12) and monosomy 21(pter----q21). A propos of a case].. PubMed. 32(5). 369–75. 3 indexed citations
20.
Rolland, M., et al.. (1977). [Partial trisomy 10p of paternal origin. 2 new cases in 2 different families].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 20(3). 209–13. 6 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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