G. Bourrouillou

999 citations
39 papers · 580 · h-index 13

Impact in

    • Sperm and Testicular Function
  • Genetics top 5%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genomic variations and chromosomal abnormalities

Papers in

G. Bourrouillou

36 papers receiving 533 citations

Peers

G. Bourrouillou
Comparison fields: 5 of 50
  • Reproductive Medicine 123
  • Genetics 367
  • Pediatrics, Perinatology and Child Health 126
  • Molecular Biology 236
  • Hematology 36
Replace J L Watt with:
J L Watt United Kingdom
Sofia Dória Portugal
Ulrike Mau Germany
Daniela Bettio Italy
Bela Patel United States
Tracy N. Hadnott United States
Gregor Schlüter Germany
Cherie A. Kessler United States
Philip N. Mowrey United States
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Citations per field
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Citations per year

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-authors

The 25 scholars most cited alongside G. Bourrouillou, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with G. Bourrouillou Line = papers co-authored together G. Bourrouillou links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 39 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2000116
2 198579
3
22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypes.
199942
4 201040
5 200432
6 201332
7 198631
8 200430
9 200422
10
[Role and contribution of karyotyping in male infertility].
199217
11
[Chromosome anomalies and male infertility. A study of 1,444 subjects].
198715
12 198813
13
A case of trisomy 12 mosaicism with pituitary malformation and polycystic ovary syndrome.
200613
14 199211
15 199211
16 198410
17
[Secondary 18q2 due to a paternal double translocation].
19839
18 20097
19
[Partial trisomy 10p of paternal origin. 2 new cases in 2 different families].
19776
20
[Partial monosomy 10p in a case investigated with tomodensitometry (author's transl)].
19816

About G. Bourrouillou

G. Bourrouillou is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Endocrinology, Diabetes and Metabolism, Molecular Biology and Surgery, having authored 39 papers that have together received 580 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (9 papers), Alkaline Phosphatase Research Studies (9 papers), Acute Myeloid Leukemia Research (4 papers), Chronic Myeloid Leukemia Treatments (4 papers), Pancreatitis Pathology and Treatment (4 papers), Congenital heart defects research (3 papers) and Connective tissue disorders research (3 papers). The work is most often cited by research in Reproductive Medicine (123 citations), Genetics (367 citations), Pediatrics, Perinatology and Child Health (126 citations), Molecular Biology (236 citations) and Hematology (36 citations). G. Bourrouillou has collaborated with scholars based in France, Belgium and United States. Frequent co-authors include Nicole Dastugue, P Colombiès, Patrick Calvas, Louis Bujan, M. Rolland, Ken McElreavey, Hassan Rouba, Jean Pierre Siffroi, D Boucher and J. P. Dadoune. Their work appears in journals such as Human Genetics, Early Human Development, Acta Haematologica, Clinica Chimica Acta and European Journal of Medical Genetics.

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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