N. J. Leschot - Concepedia

Author

N. J. Leschot

Also Known As

N J Leschot, N Leschot, N. J Leschot, N. J. LESCHOT, N. J. Leschot, N.J Leschot, N.J. (a) Leschot, N.J. Leschot, NICO J. LESCHOT, Nico J Leschot

119

Publications

3.4K

Citations

H-Index

111

Concepts

All Affiliations

University of Amsterdam Amsterdam UMC Location University of Amsterdam Leiden University Wilhelmina Children's Hospital Utrecht University

About

N. J. Leschot is an author at University of Amsterdam specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	33	1.5K
2	Public Health	12	14	518
3	Education	2	2	95
4	Natural Sciences	2	2	146
5	Health Sciences	1	1	98

N. J. Leschot

Publications

2.9K

Citations

H-Index

Page 1

	Year	Citations
Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy Edo M Hoogerwaard, Poll A. van der Wouw, Arthur A.M. Wilde, Neuromuscular Disorders Cardiac MuscleCardiomyopathyHeart FailurePhysiologyBecker Muscular Dystrophy	1999	179
Reproductive outcome after chromosome analysis in couples with two or more miscarriages: case-control study Maureen T.M. Franssen, Johanna C. Korevaar, Fulco van der Veen, BMJ	2006	158
Selective chromosome analysis in couples with two or more miscarriages: case-control study Maureen Franssen, Johanna C. Korevaar, N. J. Leschot, BMJ	2005	141
High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered J.M.N. Hoovers, M. Mannens, Rosalind M. John, Genomics Functional GenomicsHigh-resolution LocalizationMedicineGeneticsNatural Sciences	1992	131
Parental Imprinting of Human Chromosome Region 11p15.3-pter Involved in the Beckwith-Wiedemann Syndrome and Various Human Neoplasia Marcel M. A. M. Mannens, J.M.N. Hoovers, E. Redeker, European Journal of Human Genetics Beckwith-wiedemann SyndromeGenetic DisorderGeneticsPathologyMolecular Genetics	1994	108
Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells Jet Bliek, Mariëlle Alders, Saskia M. Maas, European Journal of Human Genetics Bws TwinsDevelopmental BiologyPaternal HypomethylationGenetic DisorderMedicine	2009	98
Long‐term follow‐up of infants after transcervical chorionic villus sampling and after amniocentesis to compare congenital abnormalities and health status Arty H. P. Schaap, Hans G. van der Pol, Kees Boer, Prenatal Diagnosis	2002	96
Absence of deleted in azoospermia (DAZ) genes in spermatozoa of infertile men with somatic DAZ deletions Jan W. A. de Vries, Sjoerd Repping, Robert D. Oates, Fertility and Sterility InfertilityAndrologyDevelopmental BiologyFertilityGenetics	2001	91
Jejunal atresia related to the use of methylene blue in genetic amniocentesis in twins J.G. van der Pol, Hans Wolf, Kees Boer, BJOG An International Journal of Obstetrics & Gynaecology	1992	85
Cerebral gigantism (Sotos syndrome). Compiled data of 22 cases J.M. Wit, F. A. Beemer, P. G. Barth, European Journal of Pediatrics NeuropsychologyCerebral GigantismNeurological DisorderClinical NeurologyBrain Injury	1985	84

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