Antoinet C.J. Gijsbers

Author

Leiden University Medical Center

Also Known As

Antoinet C J Gijsbers, Antoinet C. J. Gijsbers, Antoinet C.J. Gijsbers, Antoinet CJ Gijsbers, Antoinet Gijsbers

Publications

687

Citations

H-Index

Concepts

All Affiliations

Leiden University Medical Center University Medical Center Groningen Lange Land Ziekenhuis Hôpital Necker-Enfants Malades University of Twente

About

Antoinet C.J. Gijsbers is an author at Leiden University Medical Center specializing in medicine, genetics, and psychiatry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	309
2	Education	1	1	85
3	Public Health	1	1	75
4	Biostatistics	1	1	75
5	Cell Biology	1	1	17

Antoinet C.J. Gijsbers

Publications

645

Citations

H-Index

Page 1

	Year	Citations
Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances M. Doornbos, Birgit Sikkema‐Raddatz, Claudia A.L. Ruijvenkamp, European Journal of Medical Genetics Breakpoints 1PsychopathologyPsychiatryNine PatientsMicrodeletion 15Q11.2	2009	167
A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays first Antoinet C.J. Gijsbers, Janet YK Lew, Cathy A.J. Bosch, European Journal of Human Genetics Intellectual ImpairmentEarly DiagnosisPsychiatryDisabilityPediatrics	2009	85
Copy number variants in patients with short stature Hermine A. van Duyvenvoorde, Julian C. Lui, Sarina G. Kant, European Journal of Human Genetics Down SyndromeGenetic DisorderGeneticsGenetic EpidemiologyCopy Number Variants	2013	75
Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11 Christian Wentzel, Evica Rajcan‐Separovic, Claudia Ruivenkamp, European Journal of Human Genetics Interstitial DeletionsMedicineGeneticsGenetic DisorderPathology	2011	60
Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypes Antoinet C.J. Gijsbers, Cathy A.J. Bosch, Johannes G. Dauwerse, European Journal of Medical Genetics Intellectual ImpairmentAdditional Cryptic CnvsPsychiatryGenetic DisorderPsychiatric Genetics	2010	56
Copy Number Variants in Short Children Born Small for Gestational Age Jan M. Wit, Hermine A. van Duyvenvoorde, Jan B. van Klinken, Hormone Research in Paediatrics	2014	47
Molecular and clinical characterization of patients with a ring chromosome 11 Kerstin Hansson, Antoinet C.J. Gijsbers, Wilma Oostdijk, European Journal of Medical Genetics	2012	40
Genome-Wide SNP Array Analysis in Patients with Features of Sotos Syndrome Remco Visser, Antoinet C.J. Gijsbers, Claudia Ruivenkamp, Hormone Research in Paediatrics	2010	25
Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement of <i>FOXG1</i> appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus Gijs W.E. Santen, Yu Sun, Antoinet C.J. Gijsbers, Journal of Medical Genetics	2012	25
A terminal 3p26.3 deletion is not associated with dysmorphic features and intellectual disability in a four‐generation family Setareh Moghadasi, Arie van Haeringen, Lieke Langendonck, American Journal of Medical Genetics Part A	2014	20

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