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Clinton Baldwin

Research Profile

Genes & Molecular Sequences

Single Nucleotide Polymorphism

Physiology

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Fetal Hemoglobin

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Abdulrahman Alsultan; Harold Bae; Clinton T Baldwin; David H K Chui; Hong-Yuan Luo; Efthymia Melista; Zaki Nasserullah; Duyen Ngo; Paola Sebastiani; Martin H Steinberg; Ahmed M Suliman; Waleed H Albuali; Amein K Al-Ali
Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β(0) thalassemia.
Duyen Ngo; Surinder Safaya; Paola Sebastiani; Nadia Solovieff; Martin H Steinberg; Idowu Akinsheye; Muneer H Al Bagshi; Amein K Al-Ali; Waleed H Albuali; Ahmed M Al-Suliman; Harold Bae; Clinton T Baldwin; David H K Chui; John J Farrell; Lindsay A Farrer; Patrick Gallagher; Hong-Yuan Luo; Efthymia Melista; Zaki Naserullah; Abdulrahman Alsultan
Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype.
Jacqueline N Milton; Caterina P Minniti; Mehdi Nouraie ; Sohail Rana; Helen Rooks; Paola Sebastiani; James Taylor; Swee Lay Thein; Yingze Zhang; Clinton T Baldwin; Andrew Campbell; Oswaldo Castro; Emma Drasar; Mark T Gladwin; Victor R Gordeuk; Gregory R Kato; Lori Luchtman-Jones; Elizabeth L McCabe; Efthymia Melista; Martin H Steinberg
Genetic determinants of haemolysis in sickle cell anaemia.

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2013: Abdulrahman Alsultan; Harold Bae; Clinton T Baldwin; David H K Chui; Hong-Yuan Luo; Efthymia Melista; Zaki Nasserullah; Duyen Ngo; Paola Sebastiani; Martin H Steinberg; Ahmed M Suliman; Waleed H Albuali; Amein K Al-Ali
Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β(0) thalassemia.
American journal of hematology 2013;88(6):531-2.
2013: Duyen Ngo; Surinder Safaya; Paola Sebastiani; Nadia Solovieff; Martin H Steinberg; Idowu Akinsheye; Muneer H Al Bagshi; Amein K Al-Ali; Waleed H Albuali; Ahmed M Al-Suliman; Harold Bae; Clinton T Baldwin; David H K Chui; John J Farrell; Lindsay A Farrer; Patrick Gallagher; Hong-Yuan Luo; Efthymia Melista; Zaki Naserullah; Abdulrahman Alsultan
Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype.
Blood cells, molecules & diseases 2013;51(1):22-6.
2013: Jacqueline N Milton; Caterina P Minniti; Mehdi Nouraie ; Sohail Rana; Helen Rooks; Paola Sebastiani; James Taylor; Swee Lay Thein; Yingze Zhang; Clinton T Baldwin; Andrew Campbell; Oswaldo Castro; Emma Drasar; Mark T Gladwin; Victor R Gordeuk; Gregory R Kato; Lori Luchtman-Jones; Elizabeth L McCabe; Efthymia Melista; Martin H Steinberg
Genetic determinants of haemolysis in sickle cell anaemia.
British journal of haematology 2013;161(2):270-8.
2013: Badri Vardarajan; David Vergote; Jing Yang; Kunie Ando; Clinton T Baldwin; Jean-Pierre Brion; Rong Cheng; Nathalie Daude; Lindsay A Farrer; Paul E Fraser; Peter St George-Hyslop; Mahdi Ghani; André M Goffinet; Satyabrata Kar; Joseph Lee; Mark Logue; Richard Mayeux; Ekaterina Rogaeva; Beipei Shi; Fadel Tissir; David Westaway
Role of p73 in Alzheimer disease: lack of association in mouse models or in human cohorts.
Molecular neurodegeneration 2013;8():10.
2012: Harold T Bae; Clinton T Baldwin; EMILY BARRON-CASELLA; Christopher J Bean; Pallav Bhatnagar; Andrew Campbell; James F Casella; Michael R DeBaun; Melanie Garrett; Mark T Gladwin; Victor Roland Gordeuk; W Craig Hooper; Carolyn Hoppe; Gregory Kato ; JEFFREY KEEFER; Lori Luchtman-Jones; Caterina P Minniti; Paola Sebastiani; Dan E Arking; Allison Ashley-Koch; James Taylor; Marilyn J Telen; Yingze Zhang; Martin H Steinberg
Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans.
Blood 2012;120(9):1961-2.
2012: Abdulrahman Alsultan; Clinton T Baldwin; David H K Chui; John J Farrell; Lindsay Farrer; Hazem A. Ghabbour; Hong Luo; Efthymia Melista; Duyen A Ngo; Maxwell Nwaru; Surinder Safaya; Nadia Solovieff; Idowu Akinsheye; Mohammed Alabdulaali; Amein Al-Ali; Muneer Al-Baghshi; Waleed Albu-Ali; Ahmed Alsuliman; Martin H Steinberg
A functional promoter polymorphism of the δ-globin gene is a specific marker of the Arab-Indian haplotype.
American journal of hematology 2012;87(8):824-6.
2012: Scott A Melville; Antonio R Parrado; Shannon L Risacher; Andrew J. Saykin; Li Shen; Badri Vardarajan; Clinton T Baldwin; Jacqueline Buros; Charles DeCarli; Lindsay A Farrer; Gyungah Jun; Sungeun Kim; Mark W Logue; Kathryn L Lunetta
Multiple loci influencing hippocampal degeneration identified by genome scan.
Annals of neurology 2012;72(1):65-75.
2012: Porat M Erlich; Carmela R Abraham; Clinton T Baldwin; L Adrienne Cupples; Robert C Green; Kathryn L Lunetta; Lindsay A Farrer
Serum paraoxonase activity is associated with variants in the PON gene cluster and risk of Alzheimer disease.
Neurobiology of aging 2012;33(5):1015.e7-23.
2012: Jacqueline N Milton; Paola Sebastiani; Karen Soldano; Nadia Solovieff; Martin H Steinberg; Marilyn J Telen; Dan E Arking; Allison Ashley-Koch; Clinton T Baldwin; EMILY BARRON-CASELLA; Christopher J Bean; Pallav Bhatnagar; James F Casella; Michael R DeBaun; Daniel A Dworkis; Melanie E Garrett; Mark T Gladwin; Stephen W Hartley; W Craig Hooper; Elizabeth S Klings
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
PloS one 2012;7(4):e34741.
2012: Paola Sebastiani; Nadia Solovieff; Martin H Steinberg; Kyle M Walsh; Jemma B Wilk; Annibale Puca; Stacy Andersen; Clinton T Baldwin; Andrew T Dewan; Daniel A Dworkis; Stephen W Hartley; Josephine Hoh; Efthymia Melista; Monty Montano; Richard H Myers; Thomas T Perls
Genetic signatures of exceptional longevity in humans.
PloS one 2012;7(1):e29848.
2011: Mark W Logue; Kathryn L Lunetta; Thomas O Obisesan; Matthew Schu; Rhonna Shatz; Badri N Vardarajan; Clinton T Baldwin; Amy Borenstein; Jacki Buros; L Adrienne Cupples; MARGARET D FALLIN; Lindsay A Farrer; Rodney C P Go; Robert C Green; Patrick Griffith
A comprehensive genetic association study of Alzheimer disease in African Americans.
Archives of neurology 2011;68(12):1569-79.
2011: Paola Sebastiani; Nadia Solovieff; Martin H Steinberg; Jemma B Wilk; Annibale Puca; Stacy Andersen; Clinton T Baldwin; Daniel A Dworkis; Stephen W Hartley; Efthymia Melista; Monty Montano; Richard H Myers; Thomas T Perls
Retraction.
Science (New York, N.Y.) 2011;333(6041):404.
2011: Idowu Akinsheye; Abdulrahman Alsultan; Clinton T Baldwin; David H K Chui; Duyen Ngo; Paola Sebastiani; Nadia Solovieff; Martin H Steinberg
Fetal hemoglobin in sickle cell anemia.
Blood 2011;118(1):19-27.
2011: Nadia Solovieff; Stephen W Hartley; Clinton T Baldwin; Elizabeth S Klings; Mark T Gladwin; James G Taylor; Gregory Kato ; Lindsay A Farrer; Martin H Steinberg; Paola Sebastiani
Ancestry of African Americans with sickle cell disease.
Blood cells, molecules & diseases 2011;47(1):41-5.
2011: Daniel A Dworkis; Elizabeth S Klings; Nadia Solovieff; Guihua Li; Jacqueline N Milton; Stephen W Hartley; Efthymia Melista; Jason Parente; Paola Sebastiani; Martin H Steinberg; Clinton T Baldwin
Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1.
American journal of hematology 2011;86(2):220-3.
2011: Karen T Cuenco; Robert P Friedland; Clinton T Baldwin; Jianping Guo; Badri Vardarajan; Kathryn L Lunetta; L Adrienne Cupples; Robert C Green; Charles DeCarli; Lindsay A Farrer
Association of TTR polymorphisms with hippocampal atrophy in Alzheimer disease families.
Neurobiology of aging 2011;32(2):249-56.
2011: Paola Sebastiani; Martin H Steinberg; Ali Torkamani; Stacy Andersen; Clinton T Baldwin; Gary Benson; Jacqueline N Milton; Monty Montano; Phillip Pham; Alberto Riva; Eugene Scherba; Nicholas J Schork; Thomas T Perls
Whole genome sequences of a male and female supercentenarian, ages greater than 114 years.
Frontiers in genetics 2011;2():90.
2011: Richard Sherva; Clinton T Baldwin; Rivka Inzelberg; Badri Vardarajan; L Adrienne Cupples; Kathryn Lunetta; Abdalla Bowirrat; Adam Naj; Margaret Pericak-Vance; Robert P Friedland; Lindsay A Farrer
Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data.
Journal of Alzheimer's disease : JAD 2011;23(2):349-59.
2010: Paola Sebastiani; Nadia Solovieff; Martin H Steinberg; Jemma B Wilk; Annibale Puca; Stacy Andersen; Clinton T Baldwin; Daniel A Dworkis; Stephen W Hartley; Efthymia Melista; Monty Montano; Richard H Myers; Thomas T Perls
Genetic signatures of exceptional longevity in humans.
Science (New York, N.Y.) 2010;2010():.
2010: Nadia Solovieff; Jacqueline N Milton; Stephen W Hartley; Richard Sherva; Paola Sebastiani; Daniel A Dworkis; Elizabeth S Klings; Lindsay A Farrer; Melanie E Garrett; Allison Ashley-Koch; Marilyn J Telen; Supan Fucharoen; Shau-Yin Ha; Chi kong Li; David H K Chui; Clinton T Baldwin; Martin H Steinberg
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
Blood 2010;115(9):1815-22.
2010: Nadia Solovieff; Stephen W Hartley; Clinton T Baldwin; Thomas T Perls; Martin H Steinberg; Paola Sebastiani
Clustering by genetic ancestry using genome-wide SNP data.
BMC genetics 2010;11():108.
2010: Paola Sebastiani; Nadia Solovieff; Stephen W Hartley; Jacqueline N Milton; Alberto Riva; Daniel A Dworkis; Efthymia Melista; Elizabeth S Klings; Melanie E Garrett; Marilyn J Telen; Allison Ashley-Koch; Clinton T Baldwin; Martin H Steinberg
Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study.
American journal of hematology 2010;85(1):29-35.
2009: Paola Sebastiani; Monty Montano; Annibale Puca; Nadia Solovieff; Toshio Kojima; Meng C Wang; Efthymia Melista; Micah Meltzer; Sylvia E J Fischer; Stacy Andersen; Stephen H Hartley; Amanda Sedgewick; Yasumichi Arai; Aviv Bergman; Nir Barzilai; Dellara F Terry; Alberto Riva; Chiara Viviani Anselmi; Alberto Malovini; Aya Kitamoto; Motoji Sawabe; Tomio Arai; Yasuyuki Gondo; Martin H Steinberg; Nobuyoshi Hirose; Gil Atzmon; Gary Ruvkun; Clinton T Baldwin; Thomas T Perls
RNA editing genes associated with extreme old age in humans and with lifespan in C. elegans.
PloS one 2009;4(12):e8210.
2008: Karen T Cuenco; Kathryn L Lunetta; Clinton T Baldwin; Ann C McKee; Jianping Guo; L Adrienne Cupples; Robert C Green; Peter St George-Hyslop; Helena Chui; Charles DeCarli; Lindsay A Farrer
Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease.
Archives of neurology 2008;65(12):1640-8.
2008: Amanda E Sedgewick; Nadia Timofeev; Paola Sebastiani; Jason C C So; Edmond S K Ma; Li Chong Chan; Goonnapa Fucharoen; Supan Fucharoen; Cynara G Barbosa; Badri N Vardarajan; Lindsay A Farrer; Clinton T Baldwin; Martin H Steinberg; David H K Chui
BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies.
Blood cells, molecules & diseases 2008;41(3):255-8.
2008: Paola Sebastiani; Ling Wang; Vikki G Nolan; Efthymia Melista; Qianli Ma; Clinton T Baldwin; Martin H Steinberg
Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations.
American journal of hematology 2008;83(3):189-95.
2008: Zhenming Zhao; Nadia Timofeev; Stephen W Hartley; David Hk Chui; Supan Fucharoen; Thomas T Perls; Martin H Steinberg; Clinton T Baldwin; Paola Sebastiani
Imputation of missing genotypes: an empirical evaluation of IMPUTE.
BMC genetics 2008;9():85.
2008: Paola Sebastiani; Zhenming Zhao; María M Abad-Grau; Alberto Riva; Stephen W Hartley; Amanda E Sedgewick; Alessandro Doria; Monty Montano; Efthymia Melista; Dellara Terry; Thomas T Perls; Martin H Steinberg; Clinton T Baldwin
A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples.
BMC genetics 2008;9():6.
2008: D S Lee; Martin G Larson; Kathryn L Lunetta; J Dupuis; J Rong; J F Keaney; I Lipinska; Clinton T Baldwin; Ramachandran S Vasan; Emelia Benjamin
Clinical and genetic correlates of soluble P-selectin in the community.
Journal of thrombosis and haemostasis : JTH 2008;6(1):20-31.
2007: Qianli Ma; Diego F Wyszynski; John J Farrell; Abdullah Kutlar; Lindsay A Farrer; Clinton T Baldwin; Martin H Steinberg
Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.
The pharmacogenomics journal 2007;7(6):386-94.
2007: Paola Sebastiani; Vikki G Nolan; Clinton T Baldwin; María M Abad-Grau; Ling Wang; Adeboye H Adewoye; Lillian C McMahon; Lindsay A Farrer; James G Taylor; Gregory Kato ; Mark T Gladwin; Martin H Steinberg
A network model to predict the risk of death in sickle cell disease.
Blood 2007;110(7):2727-35.
2006: Dellara F Terry; Diego F Wyszynski; Vikki G Nolan; Gil Atzmon; Emily A Schoenhofen; JaeMi Pennington; Stacy L Andersen; Marsha A. Wilcox; Lindsay A Farrer; Nir Barzilai; Clinton T Baldwin; Alexzander Asea
Serum heat shock protein 70 level as a biomarker of exceptional longevity.
Mechanisms of ageing and development 2006;127(11):862-8.
2006: Abimbola Akomolafe; Kathryn L Lunetta; Porat M Erlich; L Adrienne Cupples; Clinton T Baldwin; Matthew Huyck; Robert C Green; Lindsay A Farrer
Genetic association between endothelial nitric oxide synthase and Alzheimer disease.
Clinical genetics 2006;70(1):49-56.
2006: Yan Meng; Clinton T Baldwin; Abdalla Bowirrat; Kristin Waraska; Rivka Inzelberg; Robert P Friedland; Lindsay A Farrer
Association of polymorphisms in the Angiotensin-converting enzyme gene with Alzheimer disease in an Israeli Arab community.
American journal of human genetics 2006;78(5):871-7.
2006: Porat M Erlich; Kathryn L Lunetta; L Adrienne Cupples; Matthew Huyck; Robert C Green; Clinton T Baldwin; Lindsay A Farrer
Polymorphisms in the PON gene cluster are associated with Alzheimer disease.
Human molecular genetics 2006;15(1):77-85.
2005: Christopher J Russo; Efthymia Melista; Jing Cui; Anita L DeStefano; George L Bakris; Athanasios J Manolis; Haralambos Gavras; Clinton T Baldwin
Association of NEDD4L ubiquitin ligase with essential hypertension.
Hypertension 2005;46(3):488-91.
2005: Paola Sebastiani; Marco F Ramoni; Vikki G Nolan; Clinton T Baldwin; Martin H Steinberg
Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia.
Nature genetics 2005;37(4):435-40.
2005: Abdalla Bowirrat; Jing Cui; Kristin Waraska; Robert P Friedland; Marlene Oscar-Berman; Lindsay A Farrer; Amos D Korczyn; Clinton T Baldwin
Lack of association between angiotensin-converting enzyme and dementia of the Alzheimer's type in an elderly Arab population in Wadi Ara, Israel.
Neuropsychiatric disease and treatment 2005;1(1):73-6.
2005: Xiaofeng Zhou; Jing Cui; Anita L DeStefano; Irmarie Chazaro; Lindsay A Farrer; Athanasios J Manolis; Haralambos Gavras; Clinton T Baldwin
Polymorphisms in the promoter region of catalase gene and essential hypertension.
Disease markers 2005;21(1):3-7.
2005: Jing Cui; Efthymia Melista; Irmarie Chazaro; Yuejian Zhang; Xiaofeng Zhou; Athanasios J Manolis; Clinton T Baldwin; Anita L DeStefano; Haralambos Gavras
Sequence variation of bradykinin receptors B1 and B2 and association with hypertension.
Journal of hypertension 2005;23(1):55-62.
2004: Maya Saleh; John P Vaillancourt; Graham Kyrenia Rona; Matthew Huyck; Srinivasa M Srinivasula; Emad S Alnemri; Martin H Steinberg; Vikki G Nolan; Clinton T Baldwin; Richard S Hotchkiss; Timothy G Buchman; Barbara A Zehnbauer; Michael R Hayden; Lindsay A Farrer; Sophie Roy; Donald W Nicholson
Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms.
Nature 2004;429(6987):75-9.
2004: Diego F Wyszynski; Clinton T Baldwin; M A Cleves; Y Amirault; Vikki G Nolan; John J Farrell; Alice Bisbee; Abdullah Kutlar; Lindsay A Farrer; Martin H Steinberg
Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia.
Cellular and molecular biology (Noisy-le-Grand, France) 2004;50(1):23-33.
2003: Jing Cui; Xiaofeng Zhou; Irmarie Chazaro; Anita L DeStefano; Athanasios J Manolis; Clinton T Baldwin; Haralambos Gavras
Association of polymorphisms in the promoter region of the PNMT gene with essential hypertension in African Americans but not in whites.
American journal of hypertension 2003;16(10):859-63.
2003: Porat M Erlich; Jing Cui; Irmarie Chazaro; Lindsay A Farrer; Clinton T Baldwin; Haralambos Gavras; Anita L DeStefano
Genetic variants of WNK4 in whites and African Americans with hypertension.
Hypertension 2003;41(6):1191-5.
2003: Anita L DeStefano; George A Gates; Nancy L Heard-Costa; Richard H Myers; Clinton T Baldwin
Genomewide linkage analysis to presbycusis in the Framingham Heart Study.
Archives of otolaryngology--head & neck surgery 2003;129(3):285-9.
2003: Lindsay A Farrer; Abdalla Bowirrat; Robert P Friedland; Kristin Waraska; Amos D Korczyn; Clinton T Baldwin
Identification of multiple loci for Alzheimer disease in a consanguineous Israeli-Arab community.
Human molecular genetics 2003;12(4):415-22.
2003: Lindsay A Farrer; Robert P Friedland; Abdalla Bowirrat; Kristin Waraska; Amos D Korczyn; Clinton T Baldwin
Genetic and environmental epidemiology of Alzheimer's disease in arabs residing in Israel.
Journal of molecular neuroscience : MN 2003;20(3):207-12.
2002: Lut Van Laer; Anita L DeStefano; Richard H Myers; Kris Flothmann; Sofie Thys; Erik Fransen; George A Gates; Guy Van Camp; Clinton T Baldwin
Is DFNA5 a susceptibility gene for age-related hearing impairment?
European journal of human genetics : EJHG 2002;10(12):883-6.
2002: Oscar Joost; Jemma B Wilk; L Adrienne Cupples; Michael Harmon; Amanda M Shearman; Clinton T Baldwin; George T O'Connor; Richard H Myers; Daniel J Gottlieb
Genetic loci influencing lung function: a genome-wide scan in the Framingham Study.
American journal of respiratory and critical care medicine 2002;165(6):795-9.
2002: Clinton T Baldwin; L Adrienne Cupples; Oscar Joost; Serkalem Demissie; Christine E Chaisson; JIMMY MOLYNEUX; Richard H Myers; David T Felson
Absence of linkage or association for osteoarthritis with the vitamin D receptor/type II collagen locus: the Framingham Osteoarthritis Study.
The Journal of rheumatology 2002;29(1):161-5.
2001: Saumil N Merchant; Michael J McKenna; Clinton T Baldwin; Aubrey Milunsky; Joseph B Nadol
Otopathology in a case of type I Waardenburg's syndrome.
The Annals of otology, rhinology, and laryngology 2001;110(9):875-82.
2001: Anita L DeStefano; Haralambos Gavras; Nancy L Heard-Costa; M Bursztyn; Athanasios Manolis; Lindsay A Farrer; Clinton T Baldwin; Irene Gavras; Faina Schwartz
Maternal component in the familial aggregation of hypertension.
Clinical genetics 2001;60(1):13-21.
2000: Michael Nicolaou; Anita L DeStefano; Irene Gavras; L Adrienne Cupples; Athanasios J Manolis; Clinton T Baldwin; Haralambos Gavras; Lindsay A Farrer
Genetic predisposition to stroke in relatives of hypertensives.
Stroke; a journal of cerebral circulation 2000;31(2):487-92.
1999: Faina Schwartz; Clinton T Baldwin; J Baima; Haralambos Gavras
Mitochondrial DNA mutations in patients with orthostatic hypotension.
American journal of medical genetics 1999;86(2):145-50.
1999: Clinton T Baldwin; Faina Schwartz; J Baima; M Burzstyn; Anita L DeStefano; Irene Gavras; Diane E Handy; Oscar Joost; T Martel; Athanasios Manolis; Michael Nicolaou; MR Bresnahan; Lindsay A Farrer; Haralambos Gavras
Identification of a polymorphic glutamic acid stretch in the alpha2B-adrenergic receptor and lack of linkage with essential hypertension.
American journal of hypertension 1999;12(9 Pt 1):853-7.
1999: Aubrey Milunsky; Xin Li Huang; Jeff M Milunsky; Anita L DeStefano; Clinton T Baldwin
A locus for autosomal recessive achromatopsia on human chromosome 8q.
Clinical genetics 1999;56(1):82-5.
1999: Oscar Joost; CA Taylor; CA Thomas; L Adrienne Cupples; Marie H Saint-Hilaire; Robert G Feldman; Clinton T Baldwin; Richard H Myers
Absence of effect of seven functional mutations in the CYP2D6 gene in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 1999;14(4):590-5.
1999: J Baima; Michael Nicolaou; Faina Schwartz; Anita L DeStefano; Athanasios Manolis; Irene Gavras; Cheryl L Laffer; Fernando Elijovich; Lindsay A Farrer; Clinton T Baldwin; Haralambos Gavras
Evidence for linkage between essential hypertension and a putative locus on human chromosome 17.
Hypertension 1999;34(1):4-7.
1998: Anita L DeStefano; Clinton T Baldwin; M Burzstyn; Irene Gavras; Diane E Handy; Oscar Joost; T Martel; Michael Nicolaou; Faina Schwartz; D H Streeten; Lindsay A Farrer; Haralambos Gavras
Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18q.
American journal of human genetics 1998;63(5):1425-30.
1998: Jeff M Milunsky; X L Huang; Clinton T Baldwin; M G Farah; Aubrey Milunsky
Evidence for genetic heterogeneity of the Carney complex (familial atrial myxoma syndromes).
Cancer genetics and cytogenetics 1998;106(2):173-6.
1998: Anita L DeStefano; L A Cupples; Kathleen S Arnos; JH Asher; Clinton T Baldwin; S Blanton; ML Carey; E O da Silva; Thomas B Friedman; J Greenberg; A K Lalwani; Aubrey Milunsky; Walter E Nance; Arti Pandya; Rajkumar Ramesar; A P Read; M Tassabejhi; Edward R Wilcox; Lindsay A Farrer
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations.
Human genetics 1998;102(5):499-506.
1997: Jeff M Milunsky; Anita L DeStefano; Xin Li Huang; Clinton T Baldwin; V V Michels; G Jako; Aubrey Milunsky
Familial paragangliomas: linkage to chromosome 11q23 and clinical implications.
American journal of medical genetics 1997;72(1):66-70.
1996: N T Lautenschlager; Aubrey Milunsky; Anita L DeStefano; Lindsay A Farrer; Clinton T Baldwin
A novel mutation in the MITF gene causes Waardenburg syndrome type 2.
Genetic analysis : biomolecular engineering 1996;13(2):43-4.
1996: B Bonné-Tamir; Anita L DeStefano; C E Briggs; R Adair; B Franklyn; S Weiss; Michael Korostishevsky; Moshe Frydman; Clinton T Baldwin; Lindsay A Farrer
Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.
American journal of human genetics 1996;58(6):1254-9.
1995: Clinton T Baldwin; S Weiss; Lindsay A Farrer; A L De Stefano; R Adair; B Franklyn; Kenneth K Kidd; Michael Korostishevsky; B Bonné-Tamir
Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.
Human molecular genetics 1995;4(9):1637-42.
1995: Clinton T Baldwin; C F Hoth; R A Macina; Aubrey Milunsky
Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature.
American journal of medical genetics 1995;58(2):115-22.
1995: Clinton T Baldwin; Lindsay A Farrer; R Adair; RM Dharmavaram; Sergio A Jimenez; L Anderson
Linkage of early-onset osteoarthritis and chondrocalcinosis to human chromosome 8q.
American journal of human genetics 1995;56(3):692-7.
1994: Lindsay A Farrer; K S Arnos; JH Asher; Clinton T Baldwin; S R Diehl; Thomas B Friedman; J Greenberg; K M Grundfast; C Hoth; Anil K Lalwani
Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.
American journal of human genetics 1994;55(4):728-37.
1994: Clinton T Baldwin; N R Lipsky; C F Hoth; T Cohen; W Mamuya; Aubrey Milunsky
Mutations in PAX3 associated with Waardenburg syndrome type I.
Human mutation 1994;3(3):205-11.
1993: C F Hoth; Aubrey Milunsky; N Lipsky; R Sheffer; S K Clarren; Clinton T Baldwin
Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I).
American journal of human genetics 1993;52(3):455-62.
1992: Clinton T Baldwin; C F Hoth; J A Amos; E O da-Silva; Aubrey Milunsky
An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome.
Nature 1992;355(6361):637-8.