Serieta Mohkamsing - Concepedia

Author

Serieta Mohkamsing

Erasmus University Rotterdam

Also Known As

S Mohkamsing, S. Mohkamsing, Serieta Mohkamsing

Publications

926

Citations

H-Index

Concepts

All Affiliations

Erasmus University Rotterdam

About

Serieta Mohkamsing is an author at Erasmus University Rotterdam specializing in medicine, fragile x premutation, and developmental delay.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	648
2	Public Health	1	1	46
3	Social Sciences	1	1	227
4	Immunology	1	1	178
5	Medical Laboratory Science	1	1	178

Serieta Mohkamsing

Publications

924

Citations

H-Index

Page 1

	Year	Citations
Screening and Diagnosis for the Fragile X Syndrome among the Mentally Retarded: An Epidemiological and Psychological Survey Bert de Vries, Ans M.W. van den Ouweland, Serieta Mohkamsing, The American Journal of Human Genetics DisabilityPsychological SurveyMental HealthDevelopmental DisabilitiesSocial Impairment	1997	227
Mental status of females with an FMR1 gene full mutation. Bert Ba de Vries, A. M. Wiegers, Apt Smits, PubMed	1996	207
Rapid antibody test for fragile X syndrome Rob Willemsen, Serieta Mohkamsing, Bert de Vries, The Lancet Autoimmune DiseaseMedicineImmunologyFragile X SpectrumPathology	1995	178
Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique Rob Willemsen, Arie Smits, Serieta Mohkamsing, Human Genetics Fragile X SyndromeRapid Antibody TestDiagnosisFragile X SpectrumPathology	1997	121
Screening for the fragile X syndrome among the mentally retarded: a clinical study. The Collaborative Fragile X Study Group. Bert B.A. de Vries, Serieta Mohkamsing, A.M.W. van den Ouweland, PubMed Genetic TestingGeneticsDisabilityGenetic EpidemiologyMolecular Biology	1999	46
Screening with the FMR1 protein test among mentally retarded males Bert B.A. de Vries, Serieta Mohkamsing, Ans M.W. van den Ouweland, Human Genetics PsychiatrySyndromic AutismGenetic DisorderGeneticsPsychiatric Genetics	1998	43
The fragile X phenotype in a mosaic male with a deletion showing expression of theFMR1 protein in 28% of the cells Esther de Graaff, Bert de Vries, Rob Willemsen, American Journal of Medical Genetics	1996	42
Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: a new appraisal. Rob Willemsen, F. J. LOS, Serieta Mohkamsing, Journal of Medical Genetics Fragile X SyndromeGenetic TestingDevelopmental BiologyAmniotic FluidGenetic Disorder	1997	33
Lack of Bcl10 mutations in testicular germ cell tumours and derived cell lines Evert M. van Schothorst, Serieta Mohkamsing, R. J. H. L. M. van Gurp, British Journal of Cancer	1999	27

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