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Suzanne Leal

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Pakistan

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TOP 3
Biao Li; Gao Wang; Suzanne M Leal
SimRare: a program to generate and analyze sequence-based data for association studies of quantitative and qualitative traits.
Dajiang J Liu; Suzanne M Leal
Estimating genetic effects and quantifying missing heritability explained by identified rare-variant associations.
Dajiang J Liu; Suzanne M Leal
SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations.

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All Publications

2012: Biao Li; Gao Wang; Suzanne M Leal
SimRare: a program to generate and analyze sequence-based data for association studies of quantitative and qualitative traits.
Bioinformatics (Oxford, England) 2012;28(20):2703-4.
2012: Dajiang J Liu; Suzanne M Leal
Estimating genetic effects and quantifying missing heritability explained by identified rare-variant associations.
American journal of human genetics 2012;91(4):585-96.
2012: Dajiang J Liu; Suzanne M Leal
SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations.
Bioinformatics (Oxford, England) 2012;28(13):1745-51.
2012: Kwanghyuk Lee; Regie Lyn P Santos-Cortez; Wasim Ahmad; Paula B Andrade; Muhammad Ansar; Bushra Khan; Suzanne M Leal
Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss.
American journal of medical genetics. Part A 2012;158A(2):315-21.
2012: Dajiang J Liu; Suzanne M Leal
A unified method for detecting secondary trait associations with rare variants: application to sequence data.
PLoS genetics 2012;8(11):e1003075.
2012: Dajiang J Liu; Suzanne M Leal
A unified framework for detecting rare variant quantitative trait associations in pedigree and unrelated individuals via sequence data.
Human heredity 2012;73(2):105-22.
2011: Ariel Brautbar; Daniel Covarrubias; Peter H Jones; Fremiet Lara-Garduno; Suzanne M Leal; Salim S Virani; John Belmont; Christie M Ballantyne
Variants in the APOA5 gene region and the response to combination therapy with statins and fenofibric acid in a randomized clinical trial of individuals with mixed dyslipidemia.
Atherosclerosis 2011;219(2):737-42.
2011: Atteeq U Rehman; Saima Riazuddin; Sheikh Amer Riazuddin; Mohsin Shahzad; Wasim Ahmad; Zubair M Ahmed; Rana A Ali; Paula B Andrade; Carmen C Brewer; Khitab Gul; Ateeq-Ul Jaleel; Saadullah Khan; Shaheen N Khan; Suzanne M Leal; Kwanghyuk Lee; Robert J Morell; Thomas B Friedman
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p.
Human genetics 2011;130(6):759-65.
2011: Steffie N Tomson; Rejnal Tushe; Nili Avidan; Molly S Bray; Suzanne M Leal; Kwanghyuk Lee; Dianna M Milewicz; Anand K Sarma; David M Eagleman
The genetics of colored sequence synesthesia: suggestive evidence of linkage to 16q and genetic heterogeneity for the condition.
Behavioural brain research 2011;223(1):48-52.
2011: Ellen S Regalado; Mark J Rieder; Regie L Santos-Cortez; Jay Shendure; Carlos Villamizar; Deborah A Nickerson; Nili Avidan; Francois Bernier; Aida M Bertoli Avella; Lorne Clarke; Dawna Gilchrist; Dong-Chuan Guo; Suzanne M Leal; Barbara McGillivray; Dianna M Milewicz
Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysms.
Circulation research 2011;109(6):680-6.
2011: Dongxu Lin; Jessica M Moore; P C Thornton; Ian B Gibson; Suzanne M Leal; Philip J Hastings
Global chromosomal structural instability in a subpopulation of starving Escherichia coli cells.
PLoS genetics 2011;7(8):e1002223.
2011: Shao-Qing Kuang; Callie Kwartler; Suzanne M Leal; Scott A LeMaire; Merry-Lynn N McDonald; Dianna M Milewicz; Siddharth K Prakash; Ellen S Regalado; Ludivine Russell; Hazim J Safi; Min Wang; John W Belmont; Jiu-Mei Cao; Joseph S Coselli; Anthony L Estrera; Kurt Fraivillig; Dong-Chuan Guo; Ralph J Johnson
Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections.
PLoS genetics 2011;7(6):e1002118.
2011: Sulman Basit; Kwanghyuk Lee; Rabia Habib; Leon Chen; Regie Lyn P Santos-Cortez; Zahid Azeem; Paula Andrade; Muhammad Ansar; Wasim Ahmad; Suzanne M Leal
DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2.
Human genetics 2011;129(4):379-85.
2011: Kwanghyuk Lee; Regie Lyn P Santos-Cortez; Wasim Ahmad; Muhammad Ansar; Saadullah Khan; Suzanne M Leal
A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families.
Genetics research international 2011;2011():368915.
2011: Kwanghyuk Lee; Regie Lyn P Santos-Cortez; Wasim Ahmad; Mohammad Amin Ud Din; Muhammad Ansar; Suzanne M Leal
Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX Gene.
Genetics research international 2011;2011():294675.
2011: Ghazanfar Ali; Paula B Andrade; Muhammad Ansar; Sulman Basit; Leon Chen; Jelani Musharraf; Kwanghyuk Lee; Regie Lyn P Santos-Cortez; Wasim Ahmad; Suzanne M Leal
Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3.
Human heredity 2011;71(2):106-12.
2010: Dajiang J Liu; Suzanne M Leal
Replication strategies for rare variant complex trait association studies via next-generation sequencing.
American journal of human genetics 2010;87(6):790-801.
2010: Siddharth K Prakash; Scott A LeMaire; Dong-Chuan Guo; Ludivine Russell; Ellen S Regalado; Hossein Golabbakhsh; Ralph J Johnson; Hazim J Safi; Anthony L Estrera; Joseph S Coselli; Molly S Bray; Suzanne M Leal; Dianna M Milewicz; John W Belmont
Rare copy number variants disrupt genes regulating vascular smooth muscle cell adhesion and contractility in sporadic thoracic aortic aneurysms and dissections.
American journal of human genetics 2010;87(6):743-56.
2010: Dajiang J Liu; Suzanne M Leal
A novel adaptive method for the analysis of next-generation sequencing data to detect complex trait associations with rare variants due to gene main effects and interactions.
PLoS genetics 2010;6(10):e1001156.
2010: Nicola Brunetti-Pierri; Ralph Lachman; Kwanghyuk Lee; Suzanne M Leal; Pasquale Piccolo; Ignatia B Van den Veyver; Carlos A Bacino
Terminal osseous dysplasia with pigmentary defects (TODPD): Follow-up of the first reported family, characterization of the radiological phenotype, and refinement of the linkage region.
American journal of medical genetics. Part A 2010;152A(7):1825-31.
2010: Philip J Hastings; Megan N Hersh; P C Thornton; Natalie C Fonville; Andrew Slack; Ryan L Frisch; Mellanie P Ray; Reuben S Harris; Suzanne M Leal; Susan M Rosenberg
Competition of Escherichia coli DNA polymerases I, II and III with DNA Pol IV in stressed cells.
PloS one 2010;5(5):e10862.
2009: Julie M Schultz; Shaheen N Khan; Zubair M Ahmed; Saima Riazuddin; Ali M Waryah; Dhananjay Chhatre; Matthew F Starost; Barbara Ploplis; Stephanie Buckley; David Velásquez; Madhulika Kabra; Kwanghyuk Lee; Muhammad J Hassan; Ghazanfar Ali; Muhammad Ansar; Manju Ghosh; Edward R Wilcox; Wasim Ahmad; Glenn Merlino; Suzanne M Leal; Sheikh Amer Riazuddin; Thomas B Friedman; Robert J Morell
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
American journal of human genetics 2009;85(1):25-39.
2009: Bingshan Li; Suzanne M Leal
Discovery of rare variants via sequencing: implications for the design of complex trait association studies.
PLoS genetics 2009;5(5):e1000481.
2009: Muhammad Salman Chishti; Kwanghyuk Lee; Merry-Lynn McDonald; Muhammad Jawad Hassan; Muhammad Ansar; Wasim Ahmad; Suzanne M Leal
Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3.
Journal of human genetics 2009;54(3):141-4.
2009: Bingshan Li; Suzanne M Leal
Deviations from hardy-weinberg equilibrium in parental and unaffected sibling genotype data.
Human heredity 2009;67(2):104-15.
2008: Bronson E Oosterhuis; K Steven LaForge; Dmitri Proudnikov; Ann Ho; David A Nielsen; Robert Gianotti; Sandra Barral; Derek Gordon; Suzanne M Leal; Jurg Ott; Mary Jeanne Kreek
Catechol-O-methyltransferase (COMT) gene variants: possible association of the Val158Met variant with opiate addiction in Hispanic women.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(6):793-8.
2008: Bingshan Li; Suzanne M Leal
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data.
American journal of human genetics 2008;83(3):311-21.
2008: Jeffrey T Vrabec; Liqian Liu; Bingshan Li; Suzanne M Leal
Sequence variants in host cell factor C1 are associated with Ménière's disease.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2008;29(4):561-6.
2008: Daniel Covarrubias; Ren-Kui Bai; Lee-Jun C Wong; Suzanne M Leal
Mitochondrial DNA variant interactions modify breast cancer risk.
Journal of human genetics 2008;53(10):924-8.
2008: Rob W J Collin; Ersan Kalay; Muhammad Tariq; Theo Peters; Bert van der Zwaag; Hanka Venselaar; Jaap Oostrik; Kwanghyuk Lee; Zubair M Ahmed; Refik Caylan; Yun Li; Henk A Spierenburg; Erol Eyupoglu; Angelien Heister; Saima Riazuddin; Elif Bahat; Muhammad Ansar; Selcuk Arslan; Bernd Wollnik; Han G Brunner; Cor W R J Cremers; Ahmet Karaguzel; Wasim Ahmad; Frans P M Cremers; Gert Vriend; Thomas B Friedman; Sheikh Amer Riazuddin; Suzanne M Leal; Hannie Kremer
Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.
American journal of human genetics 2008;82(1):125-38.
2008: M Salman Chishti; Attya Bhatti; Sana Tamim; Kwanghyuk Lee; Merry-Lynn McDonald; Suzanne M Leal; Wasim Ahmad
Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families.
Journal of human genetics 2008;53(2):101-5.
2008: Bingshan Li; Suzanne M Leal
Ignoring intermarker linkage disequilibrium induces false-positive evidence of linkage for consanguineous pedigrees when genotype data is missing for any pedigree member.
Human heredity 2008;65(4):199-208.
2007: A Wali; Ghazanfar Ali; Peter John; Kwanghyuk Lee; M Salman Chishti; Suzanne M Leal; Wasim Ahmad
Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2.
Annals of human genetics 2007;71(Pt 5):570-7.
2007: Ren-Kui Bai; Suzanne M Leal; Daniel Covarrubias; Aiyi Liu; Lee-Jun C Wong
Mitochondrial genetic background modifies breast cancer risk.
Cancer research 2007;67(10):4687-94.
2006: Muhammad Naeem; Jelani Musharraf; Kwanghyuk Lee; Ghazanfar Ali; M Salman Chishti; A Wali; Asma Gul; Peter John; Muhammad Jawad Hassan; Suzanne M Leal; Wasim Ahmad
Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12-q21.2.
The British journal of dermatology 2006;155(6):1184-90.
2006: A Wali; Peter John; Asma Gul; Kwanghyuk Lee; M Salman Chishti; Ghazanfar Ali; Muhammad Jawad Hassan; Suzanne M Leal; Wasim Ahmad
A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26.2-q26.31.
Clinical genetics 2006;70(3):233-9.
2006: Regie Lyn P Santos; Muhammad Jawad Hassan; Shaheen Sikandar; Kwanghyuk Lee; Ghazanfar Ali; Protacio E Martin; Michael Angelo L Wambangco; Wasim Ahmad; Suzanne M Leal
DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2.
Human genetics 2006;120(1):85-92.
2006: Aamira Tariq; Regie Lyn P Santos; Mohammad Nasim Khan; Kwanghyuk Lee; Muhammad Jawad Hassan; Wasim Ahmad; Suzanne M Leal
Localization of a novel autosomal recessive nonsyndromic hearing impairment locus DFNB65 to chromosome 20q13.2-q13.32.
Journal of molecular medicine (Berlin, Germany) 2006;84(6):484-90.
2006: Muhammad Naeem; Muhammad Wajid; Kwanghyuk Lee; Suzanne M Leal; Wasim Ahmad
A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type.
Journal of medical genetics 2006;43(3):274-9.
2006: Regie Lyn P Santos; Hatem El-Shanti; Shaheen Sikandar; Kwanghyuk Lee; Attya Bhatti; Kai Yan; Maria H Chahrour; Nathan McArthur; Thanh L Pham; Amjad Abdullah Mahasneh; Wasim Ahmad; Suzanne M Leal
Novel sequence variants in the TMIE gene in families with autosomal recessive nonsyndromic hearing impairment.
Journal of molecular medicine (Berlin, Germany) 2006;84(3):226-31.
2006: Regie Lyn P Santos; Franziska M Häfner; Patrick Huygen; Thomas E Linder; Albert Schinzel; Thomas Spillmann; Suzanne M Leal
Phenotypic characterization of DFNA24: prelingual progressive sensorineural hearing impairment.
Audiology & neuro-otology 2006;11(5):269-75.
2006: Peter John; Ghazanfar Ali; M Salman Chishti; Syed Muhammad S Naqvi; Suzanne M Leal; Wasim Ahmad
Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33-q27.3.
Human genetics 2006;118(5):665-7.
2006: Muhammad Jawad Hassan; Regie Lyn P Santos; Muhammad Arshad Rafiq; Maria H Chahrour; Thanh L Pham; Muhammad Wajid; Nadine Hijab; Michael Angelo L Wambangco; Kwanghyuk Lee; Muhammad Ansar; Kai Yan; Wasim Ahmad; Suzanne M Leal
A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3.
Human genetics 2006;118(5):605-10.
2005: Suzanne M Leal
Detection of genotyping errors and pseudo-SNPs via deviations from Hardy-Weinberg equilibrium.
Genetic epidemiology 2005;29(3):204-14.
2005: Regie Lyn P Santos; Muhammad Wajid; Mohammad Nasim Khan; Nathan McArthur; Thanh L Pham; Attya Bhatti; Kwanghyuk Lee; Saba Irshad; Asif Mir; Kai Yan; Maria H Chahrour; Muhammad Ansar; Wasim Ahmad; Suzanne M Leal
Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairment.
Human mutation 2005;26(4):396.
2005: Fuli Yu; Pardis C Sabeti; Paul Hardenbol; Qing Fu; Ben Fry; Xiuhua Lu; Sy Ghose; Richard Vega; Ag Perez; Shiran Pasternak; Suzanne M Leal; Thomas D Willis; David L Nelson; John W Belmont; Richard A Gibbs
Positive selection of a pre-expansion CAG repeat of the human SCA2 gene.
PLoS genetics 2005;1(3):e41.
2005: S Irshad; Regie Lyn P Santos; Dost Muhammad; Kwanghyuk Lee; Nathan McArthur; Sayedul Haque; Wasim Ahmad; Suzanne M Leal
Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB55 to chromosome 4q12-q13.2.
Clinical genetics 2005;68(3):262-7.
2005: Eugène Sobngwi; Jean-François Gautier; Jean-Philippe Kevorkian; Jean-Marie Villette; Jean-Pierre Riveline; Sumei Zhang; Patrick Vexiau; Suzanne M Leal; Christian Vaisse; Franck Mauvais-Jarvis
High prevalence of glucose-6-phosphate dehydrogenase deficiency without gene mutation suggests a novel genetic mechanism predisposing to ketosis-prone diabetes.
The Journal of clinical endocrinology and metabolism 2005;90(8):4446-51.
2005: John W Belmont; Suzanne M Leal
Complex phenotypes and complex genetics: an introduction to genetic studies of complex traits.
Current atherosclerosis reports 2005;7(3):180-7.
2005: Kim McBride; Ricardo H Pignatelli; Mark Lewin; Trang Ho; Susan D Fernbach; Andres Menesses; Wilbur Lam; Suzanne M Leal; Norman Kaplan; Paul Schliekelman; Jeffrey A Towbin; John W Belmont
Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability.
American journal of medical genetics. Part A 2005;134A(2):180-6.
2005: Muhammad Aslam; Muhammad Wajid; Maria H Chahrour; Muhammad Ansar; Sayedul Haque; Thanh L Pham; Regie P Santos; Kai Yan; Wasim Ahmad; Suzanne M Leal
A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3.
American journal of medical genetics. Part A 2005;133A(1):18-22.
2005: Asif Mir; Muhammad Ansar; Maria H Chahrour; Thanh L Pham; Muhammad Wajid; Sayedul Haque; Kai Yan; Wasim Ahmad; Suzanne M Leal
Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31.
American journal of medical genetics. Part A 2005;133A(1):23-6.
2005: Suzanne M Leal; Kai Yan; Bertram Müller-Myhsok
SimPed: a simulation program to generate haplotype and genotype data for pedigree structures.
Human heredity 2005;60(2):119-22.
2005: Regie Lyn P Santos; Muhammad Wajid; Thanh L Pham; J Hussan; Ghazanfar Ali; Wasim Ahmad; Suzanne M Leal
Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment.
Clinical genetics 2005;67(1):61-8.
2004: Franck Mauvais-Jarvis; Stuart B Smith; Cédric Le May; Suzanne M Leal; Jean-François Gautier; Mariam Molokhia; Jean-Pierre Riveline; Arun S Rajan; Jean-Philippe Kevorkian; Sumei Zhang; Patrick Vexiau; Michael S German; Christian Vaisse
PAX4 gene variations predispose to ketosis-prone diabetes.
Human molecular genetics 2004;13(24):3151-9.
2004: Vadim Yuferov; David Fussell; K Steven LaForge; David A Nielsen; Derek Gordon; Ann Ho; Suzanne M Leal; Jurg Ott; Mary Jeanne Kreek
Redefinition of the human kappa opioid receptor gene (OPRK1) structure and association of haplotypes with opiate addiction.
Pharmacogenetics 2004;14(12):793-804.
2004: M Aslam; Maria H Chahrour; A Razzaq; Sayedul Haque; Kai Yan; Suzanne M Leal; Wasim Ahmad
A novel locus for autosomal recessive form of hypotrichosis maps to chromosome 3q26.33-q27.3.
Journal of medical genetics 2004;41(11):849-52.
2004: Muhammad Arshad Rafiq; Muhammad Ansar; T Pham; Muhammad Amin-Ud-Din; M Anwar; Sayedul Haque; Maria H Chahrour; Kai Yan; Suzanne M Leal; Wasim Ahmad
Localization of a novel locus for hereditary nail dysplasia to chromosome 17q25.1-17q25.3.
Clinical genetics 2004;66(1):73-8.
2004: Muhammad Arshad Rafiq; Muhammad Ansar; Saqib Mahmood; Sayedul Haque; Muhammad Faiyaz-Ul-Haque; Suzanne M Leal; Wasim Ahmad
A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis.
The Journal of investigative dermatology 2004;123(1):247-8.
2004: Tong-Tong Li; Susana Larrucea; Shiloe Souza; Suzanne M Leal; José A López; Edward M Rubin; Bernhard Nieswandt; Paul F Bray
Genetic variation responsible for mouse strain differences in integrin alpha 2 expression is associated with altered platelet responses to collagen.
Blood 2004;103(9):3396-402.
2004: Muhammad Ansar; Maria H Chahrour; Muhammad Amin-Ud-Din; Muhammad Arshad; Sayedul Haque; Thanh L Pham; Kai Yan; Wasim Ahmad; Suzanne M Leal
DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22.
Human heredity 2004;57(4):195-9.
2003: Muhammad Wajid; Amir Ali Abbasi; Muhammad Ansar; Thanh L Pham; Kai Yan; Sayedul Haque; Wasim Ahmad; Suzanne M Leal
DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12.
European journal of human genetics : EJHG 2003;11(10):812-5.
2003: Muhammad Arshad Rafique; Muhammad Ansar; Syed Muhammad Jamal; Sajid Malik; Muhammad Sohail; Muhammad Faiyaz-Ul-Haque; Sayedul Haque; Suzanne M Leal; Wasim Ahmad
A locus for hereditary hypotrichosis localized to human chromosome 18q21.1.
European journal of human genetics : EJHG 2003;11(8):623-8.
2003: Suzanne M Leal
Genetic maps of microsatellite and single-nucleotide polymorphism markers: are the distances accurate?
Genetic epidemiology 2003;24(4):243-52.
2003: Parimal Das; Mehreen Hai; Claire Elcock; Suzanne M Leal; Donald T Brown; Alan H Brook; Pragna I Patel
Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia.
American journal of medical genetics. Part A 2003;118A(1):35-42.
2003: Muhammad Ansar; Mohammad Ramzan; Thanh L Pham; Kai Yan; Syed Muhammad Jamal; Sayedul Haque; Wasim Ahmad; Suzanne M Leal
Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from Pakistan.
Human heredity 2003;55(1):71-4.
2003: Muhammad Ansar; Mohammad Amin ud Din; Muhammad Arshad; Muhammad Sohail; Muhammad Faiyaz-Ul-Haque; Sayedul Haque; Wasim Ahmad; Suzanne M Leal
A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from Pakistan.
European journal of human genetics : EJHG 2003;11(1):77-80.
2003: Andrew T DeWan; Antonio R Parrado; Suzanne M Leal
A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval.
Clinical genetics 2003;63(1):39-45.
2002: Andrew Chen; K Steven LaForge; Ann Ho; Pauline F McHugh; Scott H Kellogg; Kathy Bell; Rosemary P Schluger; Suzanne M Leal; Mary Jeanne Kreek
Potentially functional polymorphism in the promoter region of prodynorphin gene may be associated with protection against cocaine dependence or abuse.
American journal of medical genetics 2002;114(4):429-35.
2002: Andrew T DeWan; Antonio R Parrado; Tara C Matise; Suzanne M Leal
Map error reduction: using genetic and sequence-based physical maps to order closely linked markers.
Human heredity 2002;54(1):34-44.
2002: Andrew T DeWan; Antonio R Parrado; Tara C Matise; Suzanne M Leal
The map problem: a comparison of genetic and sequence-based physical maps.
American journal of human genetics 2002;70(1):101-7.
2001: T Cigler; K Steven LaForge; Pauline F McHugh; S U Kapadia; Suzanne M Leal; Mary Jeanne Kreek
Novel and previously reported single-nucleotide polymorphisms in the human 5-HT(1B) receptor gene: no association with cocaine or alcohol abuse or dependence.
American journal of medical genetics 2001;105(6):489-97.
2001: Suzanne M Leal
Phenotypes and genetic analysis of psychiatric and neuropsychiatric traits.
American journal of medical genetics 2001;105(1):4-7.
2001: Anja Wille; Suzanne M Leal
Novel selection criteria for genome scans of complex traits.
Genetic epidemiology 2001;21 Suppl 1():S800-4.
2000: AA Salam; Franziska M Häfner; Thomas E Linder; Thomas Spillmann; Albert Schinzel; Suzanne M Leal
A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred.
American journal of human genetics 2000;66(6):1984-8.
2000: Franziska M Häfner; AA Salam; Thomas E Linder; D Balmer; Alessandra Baumer; Albert Schinzel; Thomas Spillmann; Suzanne M Leal
A novel locus (DFNA24) for prelingual nonprogressive autosomal dominant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindred.
American journal of human genetics 2000;66(4):1437-42.
2000: Suzanne M Leal; Jurg Ott
Effects of stratification in the analysis of affected-sib-pair data: benefits and costs.
American journal of human genetics 2000;66(2):567-75.
2000: Derek Gordon; Suzanne M Leal; Simon Heath; Jurg Ott
An analytic solution to single nucleotide polymorphism error-detection rates in nuclear families: implications for study design.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2000;():663-74.
1999: JD Winick; Maude L Blundell; Brandi L Galke; AA Salam; Suzanne M Leal; Maria Karayiorgou
Homozygosity mapping of the Achromatopsia locus in the Pingelapese.
American journal of human genetics 1999;64(6):1679-85.
1999: Suzanne M Leal; Simon Heath
Searching for alcoholism susceptibility genes using Markov chain Monte Carlo methods.
Genetic epidemiology 1999;17 Suppl 1():S217-22.
1998: Suzanne M Leal; F Demir Apaydin; C Barnwell; M Iber; T Kandogan; Markus Pfister; U Braendle; O Cura; Marvin N Schwalb; Hans-Peter Zenner; Emilia Vitale
A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9.
European journal of human genetics : EJHG 1998;6(4):341-4.
1997: Suzanne M Leal; Jurg Ott
Analysis of two-locus traits under heterogeneity for recessive versus dominant inheritance.
Genetic epidemiology 1997;14(6):1097-100.