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author = "van der Gaag, Kristiaan"
1

Found 4 documents, displaying page 1 of 1

A Worldwide Survey of Human Male Demographic History Based on Y-SNP and Y-STR Data from the HGDP–CEPH Populations

Author(s) : Shi, Wentao , Ayub, Qasim , Vermeulen, Mark , Shao, Rong-guang , Zuniga, Sofia , van der Gaag, Kristiaan , de Knijff, Peter
Description : We have investigated human male demographic history using 590 males from 51 populations in the Human Genome Diversity Project - Centre d’Étude du Polymorphisme Humain worldwide panel, typed with 37 Y-chromosomal Single Nucleotide Polymorphisms and 65 Y-chromosomal Short Tandem Repeats and analyzed w...
Repository : Europe PubMed Central
Language(s) : English

Evaluating Self-declared Ancestry of U.S. Americans with Autosomal, Y-chromosomal and Mitochondrial DNA

Author(s) : Lao, Oscar , Vallone, Peter M , Coble, Michael D , Diegoli, Toni M , van Oven, Mannis , van der Gaag, Kristiaan J , Pijpe, Jeroen
Description : The current U.S. population represents an amalgam of individuals originating mainly from four continental regions (Africa, Europe, Asia and America). To study the genetic ancestry and compare with self-declared ancestry we have analyzed paternally, maternally and bi-parentally inherited DNA markers ...
Repository : Europe PubMed Central
Language(s) : English

Worldwide Population Analysis of the 4q and 10q Subtelomeres Identifies Only Four Discrete Interchromosomal Sequence Transfers in Human Evolution

Author(s) : Lemmers, Richard J.L.F. , van der Vliet, Patrick J. , van der Gaag, Kristiaan J. , Zuniga, Sofia , Frants, Rune R.
Description : Subtelomeres are dynamic structures composed of blocks of homologous DNA sequences. These so-called duplicons are dispersed over many chromosome ends. We studied the human 4q and 10q subtelomeres, which contain the polymorphic macrosatellite repeat D4Z4 and which share high sequence similarity over ...
Repository : Europe PubMed Central
Language(s) : English

Specific Sequence Variations within the 4q35 Region Are Associated with Facioscapulohumeral Muscular Dystrophy

Author(s) : Lemmers, Richard J. L. F.  , Wohlgemuth, Mariëlle  , van der Gaag, Kristiaan J.  , van der Vliet, Patrick J. 
Description : Autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) is mainly characterized by progressive wasting and weakness of the facial, shoulder, and upper-arm muscles. FSHD is caused by contraction of the macrosatellite repeat D4Z4 on chromosome 4q35. The D4Z4 repeat is very polymorphic in leng...
Repository : Europe PubMed Central
Language(s) : English
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Found 4 documents, displaying page 1 of 1