L. Sandkuijl - Concepedia

Author

L. Sandkuijl

Also Known As

L A Sandkuijl, L SANDKUIJL, L Sandkuijl, L. A. Sandkuijl, L. Sandkuijl, L.A. Sandkuijl, LA Sandkuijl, La Sandkuijl, Sandkuijl, L, Sandkuijl, LA

Publications

Citations

H-Index

Concepts

All Affiliations

Leiden University Erasmus University Rotterdam Utrecht University Leiden University Medical Center Erasmus MC - Sophia Children’s Hospital

About

L. Sandkuijl is an author at Leiden University specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	1.4K
2	Public Health	2	2	333
3	Natural Sciences	1	1	112
4	Biostatistics	1	1	31
5	Diabetes	1	1	302

L. Sandkuijl

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36 Cornelia M. van Duijn, Marieke Dekker, Vincenzo Bonifati, The American Journal of Human Genetics Neurodegenerative DiseasesMendelian DisorderGenetic DisorderGeneticsParkinson Disease	2001	377
Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling M.G.E.M. Ausems, J. R. Verbiest, MMP Hermans, European Journal of Human Genetics Genetic TestingMendelian DisorderInherited Metabolic DiseaseGenetic EpidemiologyDiabetes	1999	302
Genetic Heterogeneity of Polycystic Kidney Disease in Europe1 Dorien J.M. Peters, L. Sandkuijl Contributions to nephrology Renal DiseaseMedicineGenetic EpidemiologyHuman PolymorphismPathology	2015	285
Involvement of the <i>CACNA1A</i> gene containing region on 19p13 in migraine with and without aura Gisela M. Terwindt, Roel A. Ophoff, Ronald van Eijk, Neurology	2001	135
Linkage-Disequilibrium Mapping of Disease Genes by Reconstruction of Ancestral Haplotypes in Founder Populations Susan K. Service, Datian Lang, Nelson B. Freimer, The American Journal of Human Genetics Haplotype DeterminationLinkage DisequilibriumGenotype-phenotype AssociationFounder PopulationsGenetics	1999	112
Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family Carolien G. F. de Kovel, Frans A. Hol, J. G. A. M. Heister, Journal of Medical Genetics	2004	74
Glycogen Storage Disease Type II: Birth Prevalence Agrees with Predicted Genotype Frequency Margreet G.E.M. Ausems, K. ten Berg, M.A. Kroos, Public Health Genomics	1999	73
Incorrect specification of marker allele frequencies: effects on linkage analysis. Nelson B. Freimer, L. Sandkuijl, Sally Blower PubMed	1993	68
Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneity. Peter Heutink, T. Haitjema, Guido J. Breedveld, Journal of Medical Genetics Mendelian DisorderGenetic DisorderGeneticsHematologyClinical Genetics	1994	68
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter. Cisca Wijmenga, L. Sandkuijl, Petra Moerer, PubMed	1992	64

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