Mauricette Jamar - Concepedia

Author

Mauricette Jamar

Centre Hospitalier Universitaire de Liège

Also Known As

M Jamar, Mauricette Jamar

Publications

860

Citations

H-Index

Concepts

All Affiliations

Centre Hospitalier Universitaire de Liège University of Liège Institute of Pathology and Genetics KU Leuven UCLouvain

About

Mauricette Jamar is an author at Centre Hospitalier Universitaire de Liège specializing in medicine, pathology, and down syndrome.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	208
2	Public Health	2	2	115
3	Health Sciences	1	1	19
4	Epidemiology	1	1	98
5	Obstetrics	1	1	17

Mauricette Jamar

Publications

819

Citations

H-Index

Page 1

	Year	Citations
Gigantism and Acromegaly Due to Xq26 Microduplications and <i>GPR101</i> Mutation Giampaolo Trivellin, Adrian Daly, Fábio R. Faucz, New England Journal of Medicine	2014	329
Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes Mariluce Riegel, Alessandra Baumer, Mauricette Jamar, Human Genetics Developmental AnomalyPediatricsPathologySubmicroscopic Terminal DeletionsUnclassified Malformation Syndromes	2001	129
Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test? Alain Verloès, Y. Gillerot, Lionel Van Maldergem, European Journal of Human Genetics Down SyndromeFertilityReproductive HealthPediatricsGenetic Epidemiology	2001	98
Improved detection of chromosomal abnormalities in chronic lymphocytic leukemia by conventional cytogenetics using CpG oligonucleotide and interleukin‐2 stimulation: A Belgian multicentric study Natalie Put, Peter Könings, Katrina Rack, Genes Chromosomes and Cancer	2009	54
GOMBO syndrome: Another ?pseudorecessive? disorder due to a cryptic translocation Alain Verloès, Sylviane Lesenfants, Mauricette Jamar, American Journal of Medical Genetics Down SyndromePathologyNeuropathologyMedicineGombo Syndrome	2000	51
The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Prenatal Diagnosis	2018	29
Morphology, cytogenetics, and survival in myelodysplasia with del(20q) or ider(20q): a multicenter study François Mullier, Sylvie Daliphard, Richard Garand, Annals of Hematology Hematological MalignancyCytogeneticsGeneticsHematologyMyeloid Neoplasia	2011	19
Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome Christian Herens, Mauricette Jamar, Maria-Luz Alvarez-Gonzalez, American Journal of Medical Genetics	1997	17
A low rate of trisomy 21 in twin-pregnancies: a cytogenetics retrospective study of 278 cases. Mauricette Jamar, C. Lemarchal PubMed Down SyndromeDevelopmental AnomalyInfertilityCytogenetics Retrospective StudyFertility	2003	17
Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies Annette Uwineza, Jean‐Hubert Caberg, Janvier Hitayezu, BMC Medical Genetics	2014	16

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