A. Pakstis

K. Kidd, J. Kidd, A. Pakstis, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Global survey of haplotype frequencies and linkage disequilibrium at the RET locus

K. Kidd, J. Kidd, A. Pakstis, 2003, European Journal of Human Genetics.

A proline-threonine substitution in codon 351 of ADH1C is common in Native Americans.

K. Kidd, J. Kidd, A. Pakstis, 2002, Alcoholism, clinical and experimental research.

Reply to Whitfield

K. Kidd, J. Kidd, A. Pakstis, 2002 .

SNPsand interpopulation genotype reconstruction from tagging

Michael W. Mahoney, K. Kidd, Petros Drineas, 2007 .

The dopamine transporter protein gene (SLC6A3): primary linkage mapping and linkage studies in Tourette syndrome.

K. Kidd, A. Pakstis, G. Uhl, 1995, Genomics.

Gene variants associated with antisocial behaviour: a latent variable approach.

E. Grigorenko, A. Pakstis, Haiqun Lin, 2013, Journal of child psychology and psychiatry, and allied disciplines.

Linkage studies on Gilles de la Tourette syndrome: what is the strategy of choice?

A. Pakstis, B. V. D. van de Wetering, P. Heutink, 1995, American journal of human genetics.

Detection of a large CTG/CAG trinucleotide repeat expansion in a Danish schizophrenia kindred.

D. Levy, K. Kidd, G. Sirugo, 1997, American journal of medical genetics.

ALFRED: An Allele Frequency Database for Microevolutionary Studies

K. Kidd, J. Kidd, A. Pakstis, 2005, Evolutionary bioinformatics online.

Haplotype block structures show significant variation among populations

Hongyu Zhao, Nianjun Liu, Anthony J Brookes, 2004, Genetic epidemiology.

North Asian population relationships in a global context

K. Kidd, J. Kidd, A. Pakstis, 2022, Scientific Reports.

Exploring interactive effects of genes and environments in etiology of individual differences in reading comprehension

E. Grigorenko, A. Pakstis, C. DeYoung, 2007, Development and Psychopathology.

Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene

K. Kidd, J. Kidd, A. Pakstis, 2008, The Pharmacogenomics Journal.

D10S20, a previously unmapped RFLP (OS-3), is located on 10q near D10S4.

J. Kidd, A. Pakstis, Y. Chen, 1988, Genomics.

Abstracts of workshop presentations (Part 6 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

Haplotype structure and positive selection at TLR1

Michael P. Snyder, K. Kidd, A. Pakstis, 2013, European Journal of Human Genetics.

Gene frequency estimates for samples of black and white twins from the Philadelphia metropolitan area

S. Scarr, A. Pakstis, H. Polesky, 1978, Human Genetics.

Multiplexed SNP detection panels for human identification

K. Kidd, J. Kidd, A. Pakstis, 2009 .

SNPs for individual identification

K. Kidd, J. Kidd, A. Pakstis, 2008 .

A global view of the OCA2-HERC2 region and pigmentation

K. Kidd, E. Grigorenko, P. Paschou, 2011, Human Genetics.

The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10.

K. Kidd, Jingshi Wu, J. Kidd, 1990, American journal of human genetics.

Metabolic diversity in human populations and correlation with genetic and ancestral geographic distances

K. Kidd, A. Pakstis, C. Scharfe, 2022, Molecular genetics and metabolism.

Assignment of the norepinephrine transporter protein (NET1) locus to chromosome 16.

K. Kidd, A. Pakstis, J. Gelernter, 1993, Genomics.

State of the Art for Microhaplotypes

K. Kidd, A. Pakstis, 2022, Genes.

Single nucleotide polymorphisms and haplotypes in Native American populations.

K. Kidd, C. Nievergelt, J. Kidd, 2011, American journal of physical anthropology.

Abstracts of workshop presentations (Part 2 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

Exclusion of close linkage of Tourette's syndrome to D1 dopamine receptor.

A. Pakstis, D. Grandy, J. Kennedy, 1993, The American journal of psychiatry.

Abstracts of workshop presentations (Part 12 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

The accuracy of statistical methods for estimation of haplotype frequencies: an example from the CD4 locus.

K K Kidd, A J Pakstis, S. Tishkoff, 2000, American journal of human genetics.

Two RFLPs at the HOX2G locus.

K. Kidd, A. Pakstis, C. Castiglione, 1991, Nucleic acids research.

Global patterns of linkage disequilibrium in Homo sapiens

Hongyu Zhao, K. Kidd, J. Kidd, 2001 .

The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus

K. Kidd, J. Kidd, A. Pakstis, 1996, Human Genetics.

Searching for a major genetic locus for affective disorder in the Old Order Amish.

K. Kidd, J. Kidd, A. Pakstis, 1987, Journal of psychiatric research.

Genetic and physical mapping and population studies of a fibronectin receptor beta-subunit-like sequence on human chromosome 19.

J. Kidd, A. Pakstis, D. Ward, 1990, Genomics.

A global view of the OCA2-HERC2 region and pigmentation

K. Kidd, E. Grigorenko, P. Paschou, 2011, Human Genetics.

Abstracts of workshop presentations pp. 1106-1116

R. L. Miller, D. Cox, D. Ledbetter, 1989 .

Abstracts of workshop presentations (Part 10 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

Vibratory Urticaria Associated with a Missense Variant in ADGRE2.

K. Kidd, J. Mullikin, A. Pakstis, 2016, The New England journal of medicine.

Genetic variation in Tunisia in the context of human diversity worldwide

K. Kidd, J. Kidd, A. Pakstis, 2016, American journal of physical anthropology.

Absence of a relationship between degree of white ancestry and intellectual skills within a black population

S. Scarr, A. Pakstis, S. Katz, 1977, Human Genetics.

Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree

K. Kidd, L. Cavalli-Sforza, J. Kidd, 1988, Nature.

Linkage disequilibrium patterns vary substantially among populations

Anthony J Brookes, Sarah L Sawyer, Kenneth K Kidd, 2005, European Journal of Human Genetics.

Bitter receptor gene (TAS2R38), 6-n-propylthiouracil (PROP) bitterness and alcohol intake.

K. Kidd, J. Kidd, A. Pakstis, 2004, Alcoholism, clinical and experimental research.

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.

Dan J Stein, F. A. Schroeder, S. E. Stewart, 2014, Journal of the American Academy of Child and Adolescent Psychiatry.

Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins.

K K Kidd, J R Kidd, A J Pakstis, 2000, American journal of human genetics.

An international two–stage genome–wide search for schizophrenia susceptibility genes

J. Weissenbach, K. Kidd, A. Pakstis, 1995, Nature Genetics.

Status of the search for a major genetic locus for affective disorder in the Old Order Amish

K. Kidd, J. Kidd, A. Pakstis, 1991, Human Genetics.

Molecular genetic studies in schizophrenia.

K. Kidd, L. Cavalli-Sforza, J. Kidd, 1989, Schizophrenia bulletin.

Progress in a genome scan for linkage in schizophrenia in a large Swedish kindred.

L. Bierut, A. Pakstis, C. Wadelius, 1994, American journal of medical genetics.

The distribution and most recent common ancestor of the 17q21 inversion in humans.

Jong Jin Kim, K. Kidd, E. Grigorenko, 2010, American journal of human genetics.

Diversification of the ADH1B Gene during Expansion of Modern Humans

Li Jin, Kenneth K Kidd, Judith R Kidd, 2011, Annals of human genetics.

Variant in the glucokinase regulatory protein (GCKR) gene is associated with fatty liver in obese children and adolescents

Hongyu Zhao, L. Groop, A. Pakstis, 2012, Hepatology.

Close linkage of MT2P1 with GC on chromosome 4.

K. Kidd, J. Kidd, A. Pakstis, 1986, Cytogenetics and cell genetics.

Linkage study of a susceptibility locus for schizophrenia in the pseudoautosomal region.

K. Kidd, J. Kidd, A. Pakstis, 1994, Schizophrenia bulletin.

Genome scan for Tourette disorder in affected-sibling-pair and multigenerational families.

S. E. Stewart, C. Sabatti, W. McMahon, 2007, American journal of human genetics.

Worldwide genetic analysis of the CFTR region.

K. Kidd, J. Kidd, A. Pakstis, 2001, American journal of human genetics.

ALFRED: An allele frequency database for anthropology.

Kei-Hoi Cheung, Kenneth K Kidd, Judith R Kidd, 2002, American journal of physical anthropology.

A Distinctive Pattern of Diversity for the TAS2R38 Gene in North Africa

K. Kidd, A. Pakstis, Sarra Elkamel, 2022, Human Biology.

Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations.

Jonathan Scott Friedlaender, K K Kidd, J R Kidd, 2000, American journal of human genetics.

Progress in the search for genetic linkage with Tourette syndrome: an exclusion map covering more than 50% of the autosomal genome.

J. Kidd, A. Pakstis, B. V. D. van de Wetering, 1991, American journal of human genetics.

Abstracts of workshop presentations (Part 11 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

Eliminating mitochondrial DNA competition for nuclear DNA primers.

K. Kidd, A. Pakstis, J. Kennedy, 1993, PCR methods and applications.

Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations

Kenneth K Kidd, Judith R Kidd, William C Speed, 2007, European Journal of Human Genetics.

Report of the nomenclature committee and the 1989 catalog of mapped genes.

A. Pakstis, T. Shows, C. Boucheix, 1989, Cytogenetics and cell genetics.

New Insight into the human genetic diversity in North African populations by genotyping of SNPs in DRD3 , CSMD1 and NRG1 genes

K. Kidd, A. Pakstis, S. Boussetta, 2022, Molecular genetics & genomic medicine.

The population genetics characteristics of a 90 locus panel of microhaplotypes

K. Kidd, A. Pakstis, M. Murtha, 2021, Human Genetics.

HAPLOT: a graphical comparison of haplotype blocks, tagSNP sets and SNP variation for multiple populations

Kenneth K. Kidd, Andrew J. Pakstis, Sheng Gu, 2005, Bioinform..

STAT3 polymorphisms in North Africa and its implication in breast cancer

K. Kidd, A. Pakstis, Sarra Elkamel, 2021, Molecular genetics & genomic medicine.

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

S. E. Stewart, C. Sabatti, N. Freimer, 2015, The American journal of psychiatry.

COMT haplotypes suggest P2 promoter region relevance for schizophrenia

K K Kidd, W Speed, J R Kidd, 2004, Molecular Psychiatry.

Genetic relationships of European, Mediterranean, and SW Asian populations using a panel of 55 AISNPs

Eida Khalaf Almohammed, K. Kidd, J. Kidd, 2019, European Journal of Human Genetics.

Abstracts of workshop presentations (Part 1 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

Understanding human DNA sequence variation.

K K Kidd, J R Kidd, A J Pakstis, 2004, The Journal of heredity.

Candidate SNPs for a universal individual identification panel

K. Kidd, J. Kidd, A. Pakstis, 2007, Human Genetics.

Conservative evolution in duplicated genes of the primate Class I ADH cluster.

K. Kidd, J. Kidd, A. Pakstis, 2007, Gene.

Genome scan for linkage to Gilles de la Tourette syndrome.

K. Kidd, L. Tsui, A. Pakstis, 1994, American journal of medical genetics.

ALFRED: an allele frequency resource for research and teaching

Kenneth K. Kidd, Haseena Rajeevan, Judith R. Kidd, 2011, Nucleic Acids Res..

Aggressive behavior, related conduct problems, and variation in genes affecting dopamine turnover.

E. Grigorenko, A. Pakstis, L. Oreland, 2010, Aggressive behavior.

Assessing linkage disequilibrium in a complex genetic system. I. Overall deviation from random association

J. Kidd, A. Pakstis, H. Zhao, 1999, Annals of human genetics.

Evaluating 130 microhaplotypes across a global set of 83 populations.

K. Kidd, A. Pakstis, R. Lagacé, 2017, Forensic science international. Genetics.

Abstracts of workshop presentations (Part 13 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

ALFRED: the ALelle FREquency Database. Update

Kei-Hoi Cheung, Perry L. Miller, Kenneth K. Kidd, 2003, Nucleic Acids Res..

Gilles de la Tourette syndrome is not linked to D2-dopamine receptor.

K. Kidd, A. Pakstis, D. Grandy, 1990, Archives of general psychiatry.

One Form of Bipolar Affective Disorder is Mapped to Chromosome 11

K. Kidd, J. Kidd, A. Pakstis, 1989 .

Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.

K. Kidd, P. Paschou, J. Kidd, 2004, American journal of human genetics.

Linkage relationships of the gene for the beta subunit of nerve growth factor (NGFB) with other chromosome 1 marker loci.

E. Shooter, H. Cann, J. Kidd, 1985, Cytogenetics and cell genetics.

Obsessive‐compulsive symptom dimensions in affected sibling pairs diagnosed with Gilles de la Tourette syndrome

W. McMahon, K. Kidd, A. Pakstis, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Exclusion of a major susceptibility locus for schizophrenia in the pseudo-autosomal region in a large Swedish kindred

J. Kidd, A. Pakstis, L. Wetterberg, 1993, Schizophrenia Research.

Segregation and linkage analyses of Tourette's syndrome and related disorders.

K. Kidd, J. Kidd, A. Pakstis, 1990, Journal of the American Academy of Child and Adolescent Psychiatry.

One large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map.

K. Kidd, J. Kidd, A. Pakstis, 1987, Henry Ford Hospital medical journal.

Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group‐specific loci: Use of restriction fragment length polymorphisms extends exclusion region

K. Kidd, J. Kidd, A. Pakstis, 1986, Genetic epidemiology.

Population variation in linkage disequilibrium across the COMT gene considering promoter region and coding region variation

K. Kidd, E. Grigorenko, J. Kidd, 2002, Human Genetics.

Population studies of polymorphisms of the serotonin transporter protein gene.

K K Kidd, J R Kidd, A J Pakstis, 1999, American journal of medical genetics.

The distinctive geographic patterns of common pigmentation variants at the OCA2 gene

K. Kidd, P. Paschou, A. Pakstis, 2020, Scientific Reports.

Tyrosine hydroxylase maps to the short arm of chromosome 11 proximal to the insulin and HRAS1 loci.

K. Kidd, J. Kidd, A. Pakstis, 1988, Genomics.

Haplotype Evolution of SLITRK 1 , a Candidate Gene for Gilles de la Tourette Syndrome

B. O’Roak, K. Kidd, A. Pakstis, 2008 .

Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmission-disequilibrium test.

J. Buxbaum, K. Kidd, A. Pakstis, 1996, American journal of human genetics.

Abstracts of workshop presentations (Part 3 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

Genetic Polymorphisms Associated with Endometriosis in Pakistani Women

A. Pakstis, H. Taylor, I. Liaqat, 2013 .

The dopamine D4 receptor gene (DRD4) is not associated with alcoholism in three Taiwanese populations: Six polymorphisms tested separately and as haplotypes

K. Kidd, A. Pakstis, H. Ko, 1997, Biological Psychiatry.

Origin and dispersal of atypical aldehyde dehydrogenase ALDH2487Lys.

K. Kidd, A. Pakstis, Ya-ping Zhang, 2009, Gene.

Considerable haplotype diversity within the 23kb encompassing the ADH7 gene.

K. Kidd, E. Grigorenko, J. Kidd, 2005, Alcoholism, clinical and experimental research.

No association between DRD2 locus and alcoholism after controlling the ADH and ALDH genotypes in Chinese Han population.

K. Kidd, A. Pakstis, H. Ko, 1999, Alcoholism, clinical and experimental research.

Microhaplotype loci are a powerful new type of forensic marker

Nnamdi E. Ihuegbu, K. Kidd, A. Pakstis, 2013 .

ALFRED: an allele frequency database for diverse populations and DNA polymorphisms

Kei-Hoi Cheung, Perry L. Miller, Kenneth K. Kidd, 2000, Nucleic Acids Res..

Abstracts of workshop presentations (Part 12 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

ALFRED: a Web-accessible allele frequency database.

P L Miller, K K Kidd, K H Cheung, 1999, Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing.

The 1985 Catalog of Mapped Genes and report of the Nomenclature Committee.

R. L. Miller, A. Pakstis, T. Shows, 1985, Cytogenetics and cell genetics.

The 1988 catalog of mapped genes and report of the nomenclature committee.

A. Pakstis, T. Shows, C. Boucheix, 1988, Cytogenetics and cell genetics.

Genetic diversity of the North African population revealed by the typing of SNPs in the DRD2/ANKK1 genomic region.

K. Kidd, A. Pakstis, Sarra Elkamel, 2021, Gene.

Abstracts of workshop presentations (Part 4 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

Variation in the catechol-O-methyltransferase Val158Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents

E. Grigorenko, A. Pakstis, C. DeYoung, 2010, Psychiatric genetics.

No association between alcoholism and multiple polymorphisms at the dopamine D2 receptor gene (DRD2) in three distinct taiwanese populations

K. Kidd, J. Kidd, A. Pakstis, 1996, Biological Psychiatry.

A multipurpose panel of microhaplotypes for casework

K. Kidd, A. Pakstis, C. Scharfe, 2022, Forensic Science International: Genetics Supplement Series.

A multipurpose panel of microhaplotypes for use with STR markers in casework.

K. Kidd, A. Pakstis, C. Scharfe, 2022, Forensic science international. Genetics.

Validation of novel forensic DNA markers using multiplex microhaplotype sequencing

K. Kidd, A. Pakstis, C. Scharfe, 2020, Forensic science international. Genetics.

Evidence of positive selection on a class I ADH locus.

Kenneth K Kidd, Judith R Kidd, William C Speed, 2007, American journal of human genetics.

Presymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A.

K. Kidd, J. Kidd, A. Pakstis, 1992, The Journal of clinical endocrinology and metabolism.

Reply to Dr. Goodman

K. Kidd, G. Sirugo, A. Pakstis, 1998 .

Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette Syndrome

B. O’Roak, K. Kidd, A. Pakstis, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Mini-haplotypes as lineage informative SNPs and ancestry inference SNPs

K. Kidd, J. Kidd, A. Pakstis, 2012, European Journal of Human Genetics.

DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism research.

K. Kidd, J. Kidd, A. Pakstis, 1996, Alcoholism, clinical and experimental research.

Expanding data and resources for forensic use of SNPs in individual identification.

Kenneth K Kidd, Judith R Kidd, William C Speed, 2012, Forensic science international. Genetics.

Linkage mapping of serotonin transporter protein gene SLC6A4 on chromosome 17

K. Kidd, A. Pakstis, J. Gelernter, 1995, Human Genetics.

ALFRED: an allele frequency database for diverse populations and DNA polymorphisms - an update

Perry L. Miller, Kei-Hoi Cheung, Kenneth K. Kidd, 2001, Nucleic Acids Res..

An historical perspective on “The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus”

K. Kidd, A. Pakstis, L. Yun, 2014, Human Genetics.