Mauricette Jamar

866 total citations
17 papers, 268 citations indexed

About

Mauricette Jamar is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mauricette Jamar has authored 17 papers receiving a total of 268 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mauricette Jamar's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Chromosomal and Genetic Variations (3 papers). Mauricette Jamar is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Chromosomal and Genetic Variations (3 papers). Mauricette Jamar collaborates with scholars based in Belgium, Rwanda and France. Mauricette Jamar's co-authors include Christian Herens, Alain Verloès, Alessandra Baumer, Mariluce Riegel, Albert Schinzel, Vinciane Dideberg, L Koulischer, Vincent Bours, Lionel Van Maldergem and Roland Schoos and has published in prestigious journals such as Human Genetics, European Journal of Human Genetics and Genes Chromosomes and Cancer.

In The Last Decade

Mauricette Jamar

17 papers receiving 254 citations

Peers

Countries citing papers authored by Mauricette Jamar

Since Specialization

Citations

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

Fields of papers citing papers by Mauricette Jamar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mauricette Jamar

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Genomic studies of multiple myeloma reveal an association between X chromosome alterations and genomic profile complexity 2016 ·Genes Chromosomes and Cancer ·(unknown), Jean‐Hubert Caberg, Stéphane Wenric, Christophe Poulet, Christian Herens, Mauricette Jamar, Claire Josse, (unknown), (unknown), Yves Béguin, André Gothot, Jo Caers, Vincent Bours	3
2	Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies 2015 ·Journal of Tropical Pediatrics ·Annette Uwineza, (unknown), Mauricette Jamar, Jean‐Hubert Caberg, (unknown), (unknown), Vincent Bours, Léon Mutesa	4
3	Pattern of congenital heart diseases in Rwandan children with genetic defects 2014 ·Pan African Medical Journal ·(unknown), Annette Uwineza, Yvan Butera, (unknown), (unknown), (unknown), (unknown), Anne‐Cecile Hellin, Mauricette Jamar, Jean‐Hubert Caberg, (unknown), Joseph Mucumbitsi, Emmanuel Rusingiza, Léon Mutesa	7
4	Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies 2014 ·BMC Medical Genetics ·Annette Uwineza, Jean‐Hubert Caberg, (unknown), (unknown), Mauricette Jamar, Vinciane Dideberg, Emmanuel Rusingiza, Vincent Bours, Léon Mutesa	11
5	A new 48, XXYY/47, XYY syndrome associated with multiple skeletal abnormalities, congenital heart disease and mental retardation 2012 ·Indian journal of human genetics ·Léon Mutesa, Mauricette Jamar, (unknown), Geneviève Pierquin, Vincent Bours	6
6	Morphology, cytogenetics, and survival in myelodysplasia with del(20q) or ider(20q): a multicenter study 2011 ·Annals of Hematology ·François Mullier, Sylvie Daliphard, Richard Garand, (unknown), (unknown), Isabelle Luquet, Pascaline Talmant, Steven Richebourg, Mauricette Jamar, Jean-Michel Dogné, C Chatelain, Lucienne Michaux, Bernard Châtelain	10
7	Improved detection of chromosomal abnormalities in chronic lymphocytic leukemia by conventional cytogenetics using CpG oligonucleotide and interleukin‐2 stimulation: A Belgian multicentric study 2009 ·Genes Chromosomes and Cancer ·(unknown), Peter Könings, Katrina Rack, Mauricette Jamar, Nadine Van Roy, (unknown), (unknown), (unknown), Geneviève Ameye, Frank Speleman, Christian Herens, Hélène A. Poirel, Yves Moreau, Anne Hagemeijer, Peter Vandenberghe, Lucienne Michaux	36
8	Deletions of the 3′ BCR and 5′ ABL regions in patients with Philadelphia-positive chronic myeloid leukemia: a one-step process occurring in about 10% of the cases without any evidence of genetic instability in the target cells 2005 ·Cancer Genetics and Cytogenetics ·(unknown), (unknown), Mauricette Jamar, Vincent Bours, Christian Herens	9
9	Subtle trisomy 12q24.3 and subtle monosomy 22q13.3: Three new cases and review 2003 ·American Journal of Medical Genetics Part A ·Laura Rodríguez, N. Martínez Guardia, Christian Herens, Mauricette Jamar, Alain Verloès, (unknown), (unknown), María Luisa Martínez‐Frías	6
10	A low rate of trisomy 21 in twin-pregnancies: a cytogenetics retrospective study of 278 cases. 2003 ·PubMed ·Mauricette Jamar, (unknown), (unknown), (unknown), (unknown)	12
11	Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test? 2001 ·European Journal of Human Genetics ·Alain Verloès, Y. Gillerot, Lionel Van Maldergem, Roland Schoos, Christian Herens, Mauricette Jamar, Vinciane Dideberg, (unknown), L Koulischer	37
12	Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes 2001 ·Human Genetics ·Mariluce Riegel, Alessandra Baumer, Mauricette Jamar, (unknown), Christian Herens, Alain Verloès, Albert Schinzel	76
13	GOMBO syndrome: Another ?pseudorecessive? disorder due to a cryptic translocation 2000 ·American Journal of Medical Genetics ·Alain Verloès, (unknown), Mauricette Jamar, Vinciane Dideberg, Christian Herens	12
14	GOMBO syndrome: Another “pseudorecessive” disorder due to a cryptic translocation 2000 ·American Journal of Medical Genetics ·Alain Verloès, (unknown), Mauricette Jamar, Vinciane Dideberg, Christian Herens	6
15	Translocation (2;3)(p21;q26) as the Sole Anomaly in a Case of Primary Myelofibrosis 1999 ·Cancer Genetics and Cytogenetics ·Christian Herens, (unknown), (unknown), (unknown), Albert Thiry, Mauricette Jamar, Nicole Schaaf‐Lafontaine, (unknown), L Koulischer	3
16	Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome 1997 ·American Journal of Medical Genetics ·Christian Herens, Mauricette Jamar, (unknown), (unknown), Jacques Lombet, (unknown), L Koulischer, Alain Verloès	15
17	Monosomy 11q: Report of two familial cases and review of the literature 1993 ·American Journal of Medical Genetics ·Roland Hustinx, Alain Verloès, (unknown), Christian Herens, Mauricette Jamar, (unknown), (unknown), L Koulischer	15

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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