M. J. Grégoire

488 total citations
14 papers, 302 citations indexed

About

M. J. Grégoire is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, M. J. Grégoire has authored 14 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in M. J. Grégoire's work include Sarcoma Diagnosis and Treatment (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). M. J. Grégoire is often cited by papers focused on Sarcoma Diagnosis and Treatment (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). M. J. Grégoire collaborates with scholars based in France and Switzerland. M. J. Grégoire's co-authors include Philippe Jonveaux, Violaine Bourdon, Ruud Berger, Cécile Arnould, Christophe Philippe, S Gilgenkrantz, C Pernot, Emmanuel Raffo, Bruno Leheup and Céline Bonnet and has published in prestigious journals such as Human Molecular Genetics, Human Genetics and American Journal of Medical Genetics.

In The Last Decade

M. J. Grégoire

13 papers receiving 296 citations

Peers

Countries citing papers authored by M. J. Grégoire

Since Specialization

Citations

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

Fields of papers citing papers by M. J. Grégoire

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. J. Grégoire. 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 M. J. Grégoire. The network helps show where M. J. Grégoire may publish in the future.

Co-authorship network of co-authors of M. J. Grégoire

This figure shows the co-authorship network connecting the top 25 collaborators of M. J. Grégoire. A scholar is included among the top collaborators of M. J. Grégoire 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 M. J. Grégoire. M. J. Grégoire 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:

14 of 14 papers shown

#	Work	Indexed citations
1	Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene 2008 ·Journal of Human Genetics ·Céline Bonnet, M. J. Grégoire, (unknown), Emmanuel Raffo, Bruno Leheup, Philippe Jonveaux	15
2	Pure de-novo 5 Mb duplication at Xp11.22–p11.23 in a male: phenotypic and molecular characterization 2006 ·Journal of Human Genetics ·Céline Bonnet, M. J. Grégoire, (unknown), Emmanuel Raffo, Bruno Leheup, Philippe Jonveaux	29
3	The Signal Transducer and Activator of Transcription STAT5b Gene Is a New Partner of Retinoic Acid Receptor in Acute Promyelocytic-Like Leukaemia 1999 ·Human Molecular Genetics ·Cécile Arnould, Christophe Philippe, Violaine Bourdon, M. J. Grégoire, Ruud Berger, Philippe Jonveaux	186
4	A new case of myxoid liposarcoma with complex rearrangement including the t(12;16)(q13;p11) 1991 ·Cancer Genetics and Cytogenetics ·(unknown), M. J. Grégoire, Claude Barlier, (unknown), M. Chery, S Gilgenkrantz	1
5	Comparative study of two X breakpoints in two cases of Synovial sarcoma with translocation (X;18)(p11.2;q11.2) 1991 ·Cancer Genetics and Cytogenetics ·S Gilgenkrantz, (unknown), (unknown), M. Chery, (unknown), M. J. Grégoire, Olga Haus, Claude Turc‐Carel	1
6	Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2; q11.2) primary change in synovial sarcomas. 1990 ·PubMed ·S Gilgenkrantz, M. Chery, (unknown), (unknown), (unknown), M. J. Grégoire, (unknown), (unknown), André Hanauer	12
7	Translocation (X;18) and loss of the other X in synovial sarcoma with rearrangement of the timp oncogene 1989 ·Cancer Genetics and Cytogenetics ·M. J. Grégoire, (unknown), (unknown), M. Chery, (unknown), S Gilgenkrantz, J. Champigneulle, (unknown), Clemens A. Schmitt	1
8	Karyotype, Immunophenotype, and Clinical Outcome: Correlations in Childhood Acute Lymphoblastic Leukemia 1987 ·Hämatologie und Bluttransfusion ·M. J. Grégoire, Marie Peeters, Marie C. Béné, Pierre Bordigoni, G Fauré, S Gilgenkrantz, D Olive, F Streiff, J Duheille	2
9	Site fragile sur le chromosome 2 (q11) dans un cas de lymphohistiocytose familiale. 1984 ·S Gilgenkrantz, M. J. Grégoire, M. Chery, Pierre Bordigoni, D Olive	0
10	Chromosome 11 et cancer. 1983 ·M. J. Grégoire, C Pernot, (unknown), M Pierson, S Gilgenkrantz	2
11	Congenital acute lymphoblastic leukemia with chromosomal abnormalities including a translocation (1;4;22) 1983 ·Cancer Genetics and Cytogenetics ·S Gilgenkrantz, (unknown), (unknown), Jacqueline Buisine, M. J. Grégoire, D Olive, (unknown), F Streiff	10
12	Association of del(11)(p15.1p12), aniridia, catalase deficiency, and cardiomyopathy 1982 ·American Journal of Medical Genetics ·S Gilgenkrantz, Clara Vigneron, M. J. Grégoire, C Pernot, (unknown), John M. Opitz	21
13	Duplication 15q22�15qter and its phenotypic expression 1981 ·Human Genetics ·M. J. Grégoire, J Boué, Claudine Junien, C Pernot, S Gilgenkrantz, L Zergollern	19
14	Proximal trisomy 13. A family with balanced reciprocal translocation t(8;13) in seven members and Robertsonian translocation t(13;14) in three members 1981 ·Human Genetics ·S Gilgenkrantz, (unknown), (unknown), M. J. Grégoire	3

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.

Explore authors with similar magnitude of impact