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Peter Propping · Study

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Peter Propping

9 works· latest 2010· 2 institutionscluster: provisional

h-index9

i109

Citations767

Works here9

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Most cited in this library

Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia2005 · 236 citations
Evidence for Linkage of Spelling Disability to Chromosome 151998 · 171 citations
Genetic Contribution to Variation in Cognitive Function: An fMRI Study in Twins2009 · 105 citations
Developmental Dyslexia – Recurrence Risk Estimates from a German Bi-Center Study Using the Single Proband Sib Pair Design2005 · 56 citations
Association analysis of the dopamine D2receptor gene in Tourette's syndrome using the haplotype relative risk method1994 · 52 citations

Works

9 shown

Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21

American Journal of Medical Genetics Part B Neuropsychiatric Genetics·2010·16 authors

29citations

Genetic Contribution to Variation in Cognitive Function: An fMRI Study in Twins

Science·2009·6 authors·Open access

105citations

Interrelationship and Familiality of Dyslexia Related Quantitative Measures

Annals of Human Genetics·2006·12 authors

44citations

Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia

The American Journal of Human Genetics·2005·20 authors·Open access

236citations

Linkage analyses of chromosomal region 18p11-q12 in dyslexia

Journal of Neural Transmission·2005·14 authors

23citations

Developmental Dyslexia – Recurrence Risk Estimates from a German Bi-Center Study Using the Single Proband Sib Pair Design

Human Heredity·2005·11 authors

56citations

Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15

European Child & Adolescent Psychiatry·1999·8 authors

51citations

Evidence for Linkage of Spelling Disability to Chromosome 15

The American Journal of Human Genetics·1998·8 authors·Open access

171citations

Association analysis of the dopamine D2receptor gene in Tourette's syndrome using the haplotype relative risk method

American Journal of Medical Genetics·1994·13 authors

52citations