P Colombiès

558 total citations
64 papers, 438 citations indexed

About

P Colombiès is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, P Colombiès has authored 64 papers receiving a total of 438 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 14 papers in Hematology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in P Colombiès's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (10 papers) and Acute Myeloid Leukemia Research (7 papers). P Colombiès is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (10 papers) and Acute Myeloid Leukemia Research (7 papers). P Colombiès collaborates with scholars based in France, Switzerland and Italy. P Colombiès's co-authors include G. Bourrouillou, Nicole Dastugue, J Ducos, J Pris, J Miguérès, Yves Cambefort, J Ruffié, Patrick Calvas, J Ducos and A Mansat and has published in prestigious journals such as Nature, The Lancet and British Journal of Haematology.

In The Last Decade

P Colombiès

56 papers receiving 401 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
P Colombiès France	12	150	127	121	93	75	64	438
Sparkes Rs United States	11	132 0.9×	143 1.1×	122 1.0×	72 0.8×	42 0.6×	30	382
J. P. M. Geraedts Netherlands	11	153 1.0×	104 0.8×	95 0.8×	105 1.1×	77 1.0×	22	422
Leonard E. Reisman United States	9	151 1.0×	106 0.8×	144 1.2×	76 0.8×	39 0.5×	15	412
KarinE. Buckton United Kingdom	6	137 0.9×	178 1.4×	103 0.9×	37 0.4×	61 0.8×	8	542
Gerald E. Bloom United States	10	137 0.9×	146 1.1×	120 1.0×	57 0.6×	35 0.5×	17	444
Nataline B. Kardon United States	13	329 2.2×	232 1.8×	85 0.7×	281 3.0×	108 1.4×	26	640
Lourdes Badı́a Spain	10	110 0.7×	111 0.9×	156 1.3×	53 0.6×	39 0.5×	28	325
Bruna Tedeschi Italy	16	209 1.4×	287 2.3×	79 0.7×	115 1.2×	64 0.9×	37	620
J Insley United Kingdom	14	199 1.3×	135 1.1×	39 0.3×	120 1.3×	41 0.5×	29	461
G Fugazza Italy	8	86 0.6×	82 0.6×	259 2.1×	38 0.4×	21 0.3×	14	389

Countries citing papers authored by P Colombiès

Since Specialization

Citations

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

Fields of papers citing papers by P Colombiès

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P Colombiès

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Ged, Cécile, François Moreau‐Gaudry, Laurence Taine, et al.. (1996). PRENATAL DIAGNOSIS IN CONGENITAL ERYTHROPOIETIC PORPHYRIA BY METABOLIC MEASUREMENT AND DNA MUTATION ANALYSIS. Prenatal Diagnosis. 16(1). 83–86. 22 indexed citations

Ducos, J, et al.. (1996). [IDENTIFICATION OF MINUTE BLOOD STAINS BY DEMONSTRATION OF GMA AND GMX ANTIGENS].. PubMed. 45. 141–4.

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

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

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

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

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

Dastugue, Nicole, J Pris, & P Colombiès. (1990). Translocation t(3;21)(q26;q22) in acute myeloblastic leukemia secondary to polycythemia vera. Cancer Genetics and Cytogenetics. 44(2). 275–276. 18 indexed citations

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

10.

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

11.

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

12.

Bourrouillou, G., A Mansat, Patrick Calvas, F Pontonnier, & P Colombiès. (1987). [Chromosome anomalies and male infertility. A study of 1,444 subjects].. PubMed. 71(215). 29–31. 14 indexed citations

13.

Bourrouillou, G., P Colombiès, & Nicole Dastugue. (1986). Chromosome studies in 2136 couples with spontaneous abortions. Human Genetics. 74(4). 399–401. 31 indexed citations

14.

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

15.

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

16.

Cambefort, Yves, et al.. (1976). Topographies des bandes chromosomiques chez Papio hamadryas. Annales de Génétique. 19(4). 14 indexed citations

17.

Bonaïti‐Pellié, Catherine, et al.. (1975). [Prevalence of etinoblastoma in the Midi-Pyrenées area].. PubMed. 18(4). 223–6. 3 indexed citations

18.

Corberand, J, et al.. (1973). [Aberrant erythrocyte indices provided by the model S Coulter Couter in patients with cold agglutinins].. PubMed. 21(5). 549–53. 1 indexed citations

19.

Ducos, J, et al.. (1970). LYMPHOCYTE RESPONSE TO P.H.A. IN PATIENTS WITH LUNG CANCER. The Lancet. 295(7656). 1111–1112. 70 indexed citations

20.

Ruffié, J, et al.. (1965). [Chromosomal anomalies and disappearance of the substance H in a patient of the O group suffering from myeloblastic leukosis].. PubMed. 5(3). 501–7. 1 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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