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A.J. Pakstis
Researcher at Yale University
Publications - 39
Citations - 2886
A.J. Pakstis is an academic researcher from Yale University. The author has contributed to research in topics: Locus (genetics) & Linkage disequilibrium. The author has an hindex of 21, co-authored 39 publications receiving 2814 citations.
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Journal ArticleDOI
Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins
Sarah A. Tishkoff,E. Dietzsch,William C. Speed,A.J. Pakstis,Judith R. Kidd,Kei-Hoi Cheung,Batsheva Bonne-Tamir,A. S. Santachiara-Benerecetti,Pedro Moral,Matthias Krings,Svante Pääbo,Elizabeth Watson,Neil Risch,Trefor Jenkins,Kenneth K. Kidd +14 more
TL;DR: A global pattern of haplotype variation and linkage disequilibrium suggests a common and recent African origin for all non-African human populations.
Journal ArticleDOI
An international two-stage genome-wide search for schizophrenia susceptibility genes.
Hans W. Moises,Liu Yang,H. Kristbjarnarson,Claudia Wiese,William Byerley,Fabio Macciardi,Volker Arolt,Douglas Blackwood,X. Liu,Barbro Sjögren,Harald N. Aschauer,Hai-Gwo Hwu,K. Jang,W.J. Livesley,James L. Kennedy,Tómas Zoega,O. Ivarsson,M.-T. Bui,M.-H. Yu,B. Havsteen,Daniel Commenges,Jean Weissenbach,Eberhard Schwinger,Irving I. Gottesman,A.J. Pakstis,Lennart Wetterberg,Kenneth K. Kidd,Tómas Helgason +27 more
TL;DR: The results of a two-stage genome-wide search for genes conferring susceptibility to schizophrenia were reported in this article. But none of these genes have been found to be associated with the HLA region on chromosome 6p.
Journal ArticleDOI
Population studies of polymorphisms of the serotonin transporter protein gene.
TL;DR: Allele frequencies for both systems show significant global variation, and consequently so do haplotype frequencies, which document a large potential for population stratification in association studies of either of these SLC6A4 polymorphisms.
Journal ArticleDOI
A Global Haplotype Analysis of the Myotonic Dystrophy Locus: Implications for the Evolution of Modern Humans and for the Origin of Myotonic Dystrophy Mutations
Sarah A. Tishkoff,A Goldman,Francesc Calafell,William C. Speed,Amos S. Deinard,Batsheva Bonne-Tamir,Judith R. Kidd,A.J. Pakstis,Trefor Jenkins,Kenneth K. Kidd +9 more
TL;DR: The pattern of haplotype diversity and linkage disequilibrium observed supports a recent African-origin model of modern human evolution and suggests that the original mutation event that gave rise to DM-causing alleles arose in a population ancestral to non-Africans prior to migration of modern humans out of Africa.
Journal ArticleDOI
Genome-wide association study of Tourette's syndrome
Jeremiah M. Scharf,Jeremiah M. Scharf,Dongmei Yu,Carol A. Mathews,Benjamin M. Neale,Benjamin M. Neale,S. E. Stewart,S. E. Stewart,Jesen Fagerness,Patrick Evans,Eric R. Gamazon,Christopher K. Edlund,Anna Tikhomirov,Lisa Osiecki,Cornelia Illmann,Anna Pluzhnikov,Anuar Konkashbaev,Lea K. Davis,Buhm Han,Jacquelyn Crane,Priya Moorjani,Priya Moorjani,Andrew Crenshaw,Melissa Parkin,Victor I. Reus,Thomas L. Lowe,Martha Rangel-Lugo,Sylvain Chouinard,Yves Dion,Simon Girard,Danielle C. Cath,Danielle C. Cath,J.H. Smit,Robert A. King,Thomas V. Fernandez,James F. Leckman,Kenneth K. Kidd,J.R. Kidd,A.J. Pakstis,Matthew W. State,Luis Diego Herrera,Roxana Romero,Eduardo Fournier,Paul Sandor,Cathy L. Barr,N. Phan,Varda Gross-Tsur,Fortu Benarroch,Yehuda Pollak,Cathy L. Budman,Cathy L. Budman,Ruth D. Bruun,Ruth D. Bruun,Gerald Erenberg,Allan L. Naarden,P. C. Lee,Nicholas T. Weiss,Barbara Kremeyer,Barbara Kremeyer,Gabriel Bedoya Berrío,Desmond Campbell,Desmond Campbell,J. C. Cardona Silgado,William Cornejo Ochoa,S. C. Mesa Restrepo,H. Müller,A. V. Valencia Duarte,A. V. Valencia Duarte,Gholson J. Lyon,Gholson J. Lyon,Mark Leppert,Jubel Morgan,Robert B. Weiss,Marco A. Grados,K. Anderson,S. Davarya,Harvey S. Singer,John T. Walkup,Joseph Jankovic,Jay A. Tischfield,Gary A. Heiman,Donald L. Gilbert,Pieter J. Hoekstra,Pieter J. Hoekstra,Mary M. Robertson,Mary M. Robertson,R. Kurlan,Chunyu Liu,J. R. Gibbs,AB Singleton,John Hardy,Eric Strengman,Eric Strengman,Roel A. Ophoff,Roel A. Ophoff,Michael Wagner,Rainald Moessner,Daniel B. Mirel,Danielle Posthuma,Danielle Posthuma,Chiara Sabatti,Eskin E,David V. Conti,James A. Knowles,Andres Ruiz-Linares,Guy A. Rouleau,Shaun Purcell,Shaun Purcell,Shaun Purcell,Peter Heutink,Ben A. Oostra,William M. McMahon,Nelson B. Freimer,Nancy J. Cox,David L. Pauls +114 more
TL;DR: This study lays the groundwork for the eventual identification of common TS susceptibility variants in larger cohorts and helps to provide a more complete understanding of the full genetic architecture of this disorder.