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au.\*:("PEARSON, Peter L")

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High sibling correlation on methylphenidate response but no association with DAT1-10R homozygosity in Dutch sibpairs with ADHD : Molecular geneticsVAN DER MEULEN, Emma M; BAKKER, Steven C; PAULS, David L et al.Journal of child psychology and psychiatry and allied disciplines (Print). 2005, Vol 46, Num 10, pp 1074-1080, issn 0021-9630, 7 p.Article

CTLA4+49 A/G and CT60 polymorphisms in Dutch coeliac disease patientsVAN BELZEN, Martine J; MULDER, Chris J. J; ZHERNAKOVA, Alexandra et al.European journal of human genetics. 2004, Vol 12, Num 9, pp 782-785, issn 1018-4813, 4 p.Article

Copy number variants on the X chromosome in women with primary ovarian insufficiencyKNAUFF, Erik A. H; BLAUW, Hylke M; PEARSON, Peter L et al.Fertility and sterility. 2011, Vol 95, Num 5, pp 1584-1588, issn 0015-0282, 5 p.Article

DAT1, DRD4, and DRD5 polymorphisms are not associated with ADHD in Dutch familiesBAKKER, Steven C; VAN DER MEULEN, Emma M; OTEMAN, Nicole et al.American journal of medical genetics. 2005, Vol 132B, Num 1, pp 50-52, issn 0148-7299, 3 p.Article

No association between 12 dopaminergic genes and schizophrenia in a large dutch sampleHOOGENDOORN, Mechteld L. C; BAKKER, Steven C; SCHNACK, Hugo G et al.American journal of medical genetics. 2005, Vol 134B, Num 1, pp 6-9, issn 0148-7299, 4 p.Article

Linkage analysis of extremely discordant and concordant sibling pairs identifies quantitative trait loci influencing variation in human menopausal ageVAN ASSELT, Kristel M; KOK, Helen S; PUTTER, Hein et al.American journal of human genetics. 2004, Vol 74, Num 3, pp 444-453, issn 0002-9297, 10 p.Article

A major non-HLA locus in celiac disease maps to chromosome 19VAN BELZEN, Martine J; MEIJER, Jos W. R; SANDKUIJL, Lodewijk A et al.Gastroenterology (New York, NY. 1943). 2003, Vol 125, Num 4, pp 1032-1041, issn 0016-5085, 10 p.Article

Identification of a new copper metabolism gene by positional cloning in a purebred dog populationVAN DE SLUIS, Bart; ROTHUIZEN, Jan; PEARSON, Peter L et al.Human molecular genetics (Print). 2002, Vol 11, Num 2, pp 165-173, issn 0964-6906Article

A genomewide screen in a four-generation Dutch family with celiac disease: Evidence for linkage to chromosomes 6 and 9VAN BELZEN, Martine J; VROLIJK, Martine M; MEIJER, Jos W. R et al.The American journal of gastroenterology. 2004, Vol 99, Num 3, pp 466-471, issn 0002-9270, 6 p.Article

Accurate determination of microsatellite allele frequencies in pooled DNA samplesSCHNACK, Hugo G; BAKKER, Steven C; VAN'T SLOT, Ruben et al.European journal of human genetics. 2004, Vol 12, Num 11, pp 925-934, issn 1018-4813, 10 p.Article

Haplotype study in Dutch SCA3 and SCA6 families: evidence for common founder mutationsVERBEEK, Dineke S; PIERSMA, Sytse J; HENNEKAM, Eric F. A. M et al.European journal of human genetics. 2004, Vol 12, Num 6, pp 441-446, issn 1018-4813, 6 p.Article

Identification of a novel SCA locus (SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21VERBEEK, Dineke S; SCHELHAAS, Jurgen H; IPPEL, Elly F et al.Human genetics. 2002, Vol 111, Num 4-5, pp 388-393, issn 0340-6717Article

Towards an understanding of the genetics of human male infertility: lessons from fliesHACKSTEIN, Johannes H. P; HOCHSTENBACH, Ron; PEARSON, Peter L et al.Trends in genetics (Regular ed.). 2000, Vol 16, Num 12, pp 565-572, issn 0168-9525Article

A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17pl3.1-17pl3.3LEZIROVITZ, Karina; PEDROSA MAESTRELLI, Sylvia Regina; HENDERSON COTRIM, Nelson et al.Human genetics. 2008, Vol 123, Num 6, pp 625-631, issn 0340-6717, 7 p.Article

Heart disease risk determines menopausal age rather than the reverse. CommentaryKOK, Helen S; VAN ASSELT, Kristel M; VAN DER SCHOUW, Yvonne T et al.Journal of the American College of Cardiology. 2006, Vol 47, Num 10, pp 1976-1986, issn 0735-1097, 11 p.Article

Role of genetic analyses in cardiology Part II: Heritability estimation for gene searching in multifactorial diseasesVAN ASSELT, Kristel M; KOK, Helen S; VAN DER SCHOUW, Yvonne T et al.Circulation (New York, N.Y.). 2006, Vol 113, Num 8, pp 1136-1139, issn 0009-7322, 4 p.Article

Age at natural menopause is not linked with the follicle-stimulating hormone receptor region: a sib-pair studyKOK, Helen S; VAN ASSELT, Kristel M; PEETERS, Petra H. M et al.Fertility and sterility. 2004, Vol 81, Num 3, pp 611-616, issn 0015-0282, 6 p.Article

The recurrent translocation t(14;20)(q32;q12) in multiple myeloma results in aberrant expression of MAFB: a molecular and genetic analysis of the chromosomal breakpointBOERSMA-VREUGDENHIL, Gienke R; KUIPERS, Jeroen; VAN STRALEN, Esther et al.British journal of haematology. 2004, Vol 126, Num 3, pp 355-363, issn 0007-1048, 9 p.Article

Heritability of menopausal age in mothers and daughtersVAN ASSELT, Kristel M; KOK, Helen S; PEARSON, Peter L et al.Fertility and sterility. 2004, Vol 82, Num 5, pp 1348-1351, issn 0015-0282, 4 p.Article

Subfertility reflects accelerated ovarian ageingKOK, Helen S; VAN ASSELT, Kristel M; VAN DER SCHOUW, Yvonne T et al.Human reproduction (Oxford. Print). 2003, Vol 18, Num 3, pp 644-648, issn 0268-1161, 5 p.Article

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