Works matching AU Baldwin, Clinton

Results: 56

Rarity of the Alzheimer Disease-Protective APP A673T Variant in the United States.

Published in:

JAMA Neurology, 2015, v. 72, n. 2, p. 209, doi. 10.1001/jamaneurol.2014.2157

By:

Li-San Wang;
Naj, Adam C.;
Graham, Robert R.;
Crane, Paul K.;
Kunkle, Brian W.;
Cruchaga, Carlos;
Murcia, Josue D. Gonzalez;
Cannon-Albright, Lisa;
Baldwin, Clinton T.;
Zetterberg, Henrik;
Blennow, Kaj;
Kukull, Walter A.;
Faber, Kelley M.;
Schupf, Nicole;
Norton, Maria C.;
Tschanz, JoAnn T.;
Munger, Ronald G.;
Corcoran, Christopher D.;
Rogaeva, Ekaterina;
Chiao-Feng Lin

Publication type:

Article

Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease.

Published in:

JAMA Neurology, 2014, v. 71, n. 11, p. 1394, doi. 10.1001/jamaneurol.2014.1491

By:

Naj, Adam C.;
Gyungah Jun;
Reitz, Christiane;
Kunkle, Brian W.;
Perry, William;
Yo Son Park;
Beecham, Gary W.;
Rajbhandary, Ruchita A.;
Hamilton-Nelson, Kara L.;
Li-San Wang;
Kauwe, John S. K.;
Huentelman, Matthew J.;
Myers, Amanda J.;
Bird, Thomas D.;
Boeve, Bradley F.;
Baldwin, Clinton T.;
Jarvik, Gail P.;
Crane, Paul K.;
Rogaeva, Ekaterina;
Barmada, M. Michael

Publication type:

Article

Is DFNA5 a susceptibility gene for age-related hearing impairment?

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 12, p. 883, doi. 10.1038/sj.ejhg.5200878

By:

Van Laer, Lut;
DeStefano, Anita L;
Myers, Richard H;
Flothmann, Kris;
Thys, Sofie;
Fransen, Erik;
Gates, George A;
Van Camp, Guy;
Baldwin, Clinton T

Publication type:

Article

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.

Published in:

Nature Genetics, 2012, v. 44, n. 12, p. 1349, doi. 10.1038/ng.2466

By:

Whitcomb, David C;
LaRusch, Jessica;
Krasinskas, Alyssa M;
Klei, Lambertus;
Smith, Jill P;
Brand, Randall E;
Neoptolemos, John P;
Lerch, Markus M;
Tector, Matt;
Sandhu, Bimaljit S;
Guda, Nalini M;
Orlichenko, Lidiya;
Albert, Marilyn S;
Albin, Roger L;
Apostolova, Liana G;
Arnold, Steven E;
Baldwin, Clinton T;
Barber, Robert;
Barnes, Lisa L;
Beach, Thomas G

Publication type:

Article

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease.

Published in:

Nature Genetics, 2007, v. 39, n. 2, p. 168, doi. 10.1038/ng1943

By:

Rogaeva, Ekaterina;
Yan Meng;
Lee, Joseph H.;
Yongjun Gu;
Kawarai, Toshitaka;
Fanggeng Zou;
Katayama, Taiichi;
Baldwin, Clinton T.;
Cheng, Rong;
Hasegawa, Hiroshi;
Fusheng Chen;
Shibata, Nobuto;
Lunetta, Kathryn L.;
Pardossi-Piquard, Raphaelle;
Bohm, Christopher;
Wakutani, Yosuke;
Cupples, L. Adrienne;
Cuenco, Karen T.;
Green, Robert C.;
Pinessi, Lorenzo

Publication type:

Article

Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia.

Published in:

Nature Genetics, 2005, v. 37, n. 4, p. 435, doi. 10.1038/ng1533

By:

Sebastiani, Paola;
Ramoni, Marco F;
Nolan, Vikki;
Baldwin, Clinton T;
Steinberg, Martin H

Publication type:

Article

Absence of effect of seven functional mutations in the cyp2d6 gene in Parkinson's disease.

Published in:

Movement Disorders, 1999, v. 14, n. 4, p. 590, doi. 10.1002/1531-8257(199907)14:4<590::AID-MDS1007>3.0.CO;2-2

By:

Joost, Oscar;
Taylor, Catherine A.;
Thomas, Catherine A.;
Cupples, L. Adrienne;
Saint-Hilaire, Marie H.;
Feldman, Robert G.;
Baldwin, Clinton T.;
Myers, Richard H.

Publication type:

Article

Genome-Wide Meta-Analysis of Systolic Blood Pressure in Children with Sickle Cell Disease.

Published in:

PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0074193

By:

Bhatnagar, Pallav;
Barron-Casella, Emily;
Bean, Christopher J.;
Milton, Jacqueline N.;
Baldwin, Clinton T.;
Steinberg, Martin H.;
DeBaun, Michael;
Casella, James F.;
Arking, Dan E.

Publication type:

Article

A Genome-Wide Association Study of Total Bilirubin and Cholelithiasis Risk in Sickle Cell Anemia.

Published in:

PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0034741

By:

Milton, Jacqueline N.;
Sebastiani, Paola;
Solovieff, Nadia;
Hartley, Stephen W.;
Bhatnagar, Pallav;
Arking, Dan E.;
Dworkis, Daniel A.;
Casella, James F.;
Barron-Casella, Emily;
Bean, Christopher J.;
Hooper, W. Craig;
DeBaun, Michael R.;
Garrett, Melanie E.;
Soldano, Karen;
Telen, Marilyn J.;
Ashley-Koch, Allison;
Gladwin, Mark T.;
Baldwin, Clinton T.;
Steinberg, Martin H.;
Klings, Elizabeth S.

Publication type:

Article

Genetic Signatures of Exceptional Longevity in Humans.

Published in:

PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0029848

By:

Sebastiani, Paola;
Solovieff, Nadia;
DeWan, Andrew T.;
Walsh, Kyle M.;
Puca, Annibale;
Hartley, Stephen W.;
Melista, Efthymia;
Andersen, Stacy;
Dworkis, Daniel A.;
Wilk, Jemma B.;
Myers, Richard H.;
Steinberg, Martin H.;
Montano, Monty;
Baldwin, Clinton T.;
Hoh, Josephine;
Perls, Thomas T.

Publication type:

Article

Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.

Published in:

2013

By:

Reitz, Christiane;
Jun, Gyungah;
Naj, Adam;
Rajbhandary, Ruchita;
Vardarajan, Badri Narayan;
Wang, Li-San;
Valladares, Otto;
Lin, Chiao-Feng;
Larson, Eric B;
Graff-Radford, Neill R;
Evans, Denis;
De Jager, Philip L;
Crane, Paul K;
Buxbaum, Joseph D;
Murrell, Jill R;
Raj, Towfique;
Ertekin-Taner, Nilufer;
Logue, Mark;
Baldwin, Clinton T;
Green, Robert C

Publication type:

journal article

Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ε4 and the Risk of Late-Onset Alzheimer Disease in African Americans.

Published in:

JAMA: Journal of the American Medical Association, 2013, v. 309, n. 14, p. 1483, doi. 10.1001/jama.2013.2973

By:

Reitz, Christiane;
Jun, Gyungah;
Naj, Adam;
Rajbhandary, Ruchita;
Vardarajan, Badri Narayan;
Li-San Wang;
Valladares, Otto;
Chiao-Feng Lin;
Larson, Eric B.;
Graff-Radford, Neill R.;
Evans, Denis;
De Jager, Philip L.;
Crane, Paul K.;
Buxbaum, Joseph D.;
Murrell, Jill R.;
Raj, Towfique;
Ertekin-Taner, Nilufer;
Logue, Mark;
Baldwin, Clinton T.;
Green, Robert C.

Publication type:

Article

Identification of a dominant MYH11 causal variant in chronic intestinal pseudo‐obstruction: Results of whole‐exome sequencing.

Published in:

Clinical Genetics, 2019, v. 96, n. 5, p. 473, doi. 10.1111/cge.13617

By:

Dong, Weilai;
Baldwin, Clinton;
Choi, Jungmin;
Milunsky, Jeff M.;
Zhang, Junhui;
Bilguvar, Kaya;
Lifton, Richard P.;
Milunsky, Aubrey

Publication type:

Article

Protective variant for hippocampal atrophy identified by whole exome sequencing.

Published in:

Annals of Neurology, 2015, v. 77, n. 3, p. 547, doi. 10.1002/ana.24349

By:

Nho, Kwangsik;
Kim, Sungeun;
Risacher, Shannon L.;
Shen, Li;
Corneveaux, Jason J.;
Swaminathan, Shanker;
Lin, Hai;
Ramanan, Vijay K.;
Liu, Yunlong;
Foroud, Tatiana M.;
Inlow, Mark H.;
Siniard, Ashley L.;
Reiman, Rebecca A.;
Aisen, Paul S.;
Petersen, Ronald C.;
Green, Robert C.;
Jack, Clifford R.;
Weiner, Michael W.;
Baldwin, Clinton T.;
Lunetta, Kathryn L.

Publication type:

Article

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.

Published in:

Human Molecular Genetics, 1995, v. 4, n. 9, p. 1637

By:

Baldwin, Clinton T.;
Weiss, Sari;
Farrer, Lindsay A.;
De Stefano, Anita L.;
Adair, Ronald;
Franklyn, Barbara;
Kidd, Kenneth K.;
Korostishevsky, Michael;
Bonné-Tamir, Batsheva

Publication type:

Article

Cloning of Full-length Elastin cDNAs from a Human Skin Fibroblast Recombinant cDNA Library: Further Elucidation of Alternative Splicing Utilizing Exon-specific Oligonucleotides.

Published in:

Journal of Investigative Dermatology, 1988, v. 91, n. 5, p. 458, doi. 10.1111/1523-1747.ep12476591

By:

Fazio, Michael J.;
Olsen, David R.;
Kauh, Eunkyung A.;
Baldwin, Clinton T.;
Indik, Zena;
Ornstein-Goldstein, Norma;
Yeh, Helena;
Rosenbloom, Joel;
Uitto, Jouni

Publication type:

Article

Multiple loci influencing hippocampal degeneration identified by genome scan.

Published in:

Annals of Neurology, 2012, v. 72, n. 1, p. 65, doi. 10.1002/ana.23644

By:

Melville, Scott A.;
Buros, Jacqueline;
Parrado, Antonio R.;
Vardarajan, Badri;
Logue, Mark W.;
Shen, Li;
Risacher, Shannon L.;
Kim, Sungeun;
Jun, Gyungah;
DeCarli, Charles;
Lunetta, Kathryn L.;
Baldwin, Clinton T.;
Saykin, Andrew J.;
Farrer, Lindsay A.

Publication type:

Article

Genome-wide association study of Alzheimer's-related brain MRI traits identifies several loci influencing degeneration of the hippocampus

Published in:

2012

By:

Melville, Scott;
Buros, Jacqueline;
Parrado, Tony;
Vardarajan, Badri;
Shen, Li;
Risacher, Shannon;
Kim, Sungeun;
Jun, Gyungah;
DeCarli, Charles;
Lunetta, Kathryn;
Baldwin, Clinton;
Saykin, Andrew;
Farrer, Lindsay

Publication type:

Abstract

Candidate gene study in the endosome-to-Golgi retrieval pathway reveals association of retromer genes with Alzheimer's disease

Published in:

2010

By:

Vardarajan, Badri N.;
Logue, Mark;
Cupples, Adrienne;
Lunetta, Kathryn;
Jun, Gyungah;
Buros, Jacki;
Seaman, Matthew;
Baldwin, Clinton;
Farrer, Lindsay

Publication type:

Abstract

O2-06-08: Distinct variants in SORL1 are associated with cerebrovascular and neurodegenerative changes related to Alzheimer's disease

Published in:

2008

By:

Farrer, Lindsay A.;
Cuenco, Karen T.;
Lunetta, Kathryn;
Baldwin, Clinton T.;
McKee, Ann C.;
Guo, Jianping;
Cupples, L. Adrienne;
Green, Robert C.;
St. George-Hyslop, Peter H.;
Chui, Helena;
DeCarli, Charles

Publication type:

Abstract

Polymorphisms in paraoxonase genes PON1, PON2 and PON3 are associated with late onset Alzheimer disease

Published in:

2005

By:

Erlich, Porat M.;
Lunetta, Kathryn L.;
Cupples, L. Adrienne;
Green, Robert C.;
Baldwin, Clinton T.;
Farrer, Lindsay A.

Publication type:

Abstract

Genetic and environmental epidemiology of Alzheimer’s disease in arabs residing in Israel.

Published in:

Journal of Molecular Neuroscience, 2003, v. 20, n. 3, p. 207, doi. 10.1385/JMN:20:3:207

By:

Farrer, Lindsay;
Friedland, Robert;
Bowirrat, Abdalla;
Waraska, Kristin;
Korczyn, Amos;
Baldwin, Clinton

Publication type:

Article

Genetic and environmental risk factors for alzheimer’s disease in israeli arabs.

Published in:

Journal of Molecular Neuroscience, 2002, v. 19, n. 1/2, p. 239, doi. 10.1007/s12031-002-0040-4

By:

Bowirrat, Abdalla;
Friedland, Robert;
Farrer, Lindsay;
Baldwin, Clinton;
Korczyn, Amos

Publication type:

Article

Polymorphisms in the PON gene cluster are associated with Alzheimer disease.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 1, p. 77, doi. 10.1093/hmg/ddi428

By:

Erlich, Porat M.;
Lunetta, Kathryn L.;
Adrienne Cupples, L.;
Huyck, Matthew;
Green, Robert C.;
Baldwin, Clinton T.;
Farrer, Lindsay A.

Publication type:

Article

Identification of multiple loci for Alzheimer disease in a consanguineous Israeli–Arab community.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 4, p. 415, doi. 10.1093/hmg/ddg037

By:

Farrer, Lindsay A.;
Bowirrat, Abdalla;
Friedland, Robert P.;
Waraska, Kristin;
Korczyn, Amos D.;
Baldwin, Clinton T.

Publication type:

Article

Association of Polymorphisms of IGF1R and Genes in the Transforming Growth Factor--β/Bone Morphogenetic Protein Pathway with Bacteremia in Sickle Cell Anemia.

Published in:

Clinical Infectious Diseases, 2006, v. 43, n. 5, p. 593, doi. 10.1086/506356

By:

Adewoye, Adeboye H.;
Nolan, Vikki G.;
Qianli Ma;
Baldwin, Clinton;
Wyszynski, Diego F.;
Farrell, John J.;
Farrer, Lindsay A.;
Steinberg, Martin H.

Publication type:

Article

Role of p73 in Alzheimer disease: lack of association in mouse models or in human cohorts.

Published in:

Molecular Neurodegeneration, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1326-8-10

By:

Vardarajan, Badri;
Vergote, David;
Tissir, Fadel;
Logue, Mark;
Jing Yang;
Daude, Nathalie;
Ando, Kunie;
Rogaeva, Ekaterina;
Lee, Joseph;
Cheng, Rong;
Brion, Jean-Pierre;
Ghani, Mahdi;
Shi, Beipei;
Baldwin, Clinton T.;
Kar, Satyabrata;
Mayeux, Richard;
Fraser, Paul;
Goffinet, André M.;
George-Hyslop, Peter St;
Farrer, Lindsay A.

Publication type:

Article

Prenatal diagnosis of chronic intestinal pseudo-obstruction and paternal somatic mosaicism for the ACTG2 pathogenic variant.

Published in:

2017

By:

Milunsky, Aubrey;
Lazier, Joanna;
Baldwin, Clinton;
Young, Carmen;
Primack, Daniel;
Milunsky, Jeff M.

Publication type:

journal article

Genetic determinants of haemolysis in sickle cell anaemia.

Published in:

British Journal of Haematology, 2013, v. 161, n. 2, p. 270, doi. 10.1111/bjh.12245

By:

Milton, Jacqueline N.;
Rooks, Helen;
Drasar, Emma;
McCabe, Elizabeth L.;
Baldwin, Clinton T.;
Melista, Efi;
Gordeuk, Victor R.;
Nouraie, Mehdi;
Kato, Gregory R.;
Minniti, Caterina;
Taylor, James;
Campbell, Andrew;
Luchtman‐Jones, Lori;
Rana, Sohail;
Castro, Oswaldo;
Zhang, Yingze;
Thein, Swee Lay;
Sebastiani, Paola;
Gladwin, Mark T.;
Steinberg, Martin H.

Publication type:

Article

Clustering by genetic ancestry using genome-wide SNP data.

Published in:

BMC Genetics, 2010, v. 11, p. 108, doi. 10.1186/1471-2156-11-108

By:

Solovieff, Nadia;
Hartley, Stephen W.;
Baldwin, Clinton T.;
Perls, Thomas T.;
Steinberg, Martin H.;
Sebastiani, Paola

Publication type:

Article

A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples.

Published in:

BMC Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2156-9-6

By:

Sebastiani, Paola;
Zhenming Zhao;
Abad-Grau, Maria M.;
Riva, Alberto;
Hartley, Stephen W.;
Sedgewick, Amanda E.;
Doria, Alessandro;
Montano, Monty;
Melista, Efthymia;
Terry, Dellara;
Perls, Thomas T.;
Steinberg, Martin H.;
Baldwin, Clinton T.

Publication type:

Article

Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms.

Published in:

Nature, 2004, v. 429, n. 6987, p. 75, doi. 10.1038/nature02451

By:

Saleh, Maya;
Vaillancourt, John P.;
Graham, Rona K.;
Huyck, Matthew;
Srinivasula, Srinivasa M.;
Alnemri, Emand S.;
Steinberg, Martin H.;
Nolan, Vikki;
Baldwin, Clinton T.;
Hotchkiss, Richard S.;
Buchman, Timothy G.;
Zehnbauer, Barbara A.;
Hayden, Michael R.;
Farrer, Lindsay A.;
Roy, Sophie;
Nicholson, Donald W.

Publication type:

Article

The Dopamine D3 Receptor Gene and Posttraumatic Stress Disorder.

Published in:

Journal of Traumatic Stress, 2014, v. 27, n. 4, p. 379, doi. 10.1002/jts.21937

By:

Wolf, Erika J.;
Mitchell, Karen S.;
Logue, Mark W.;
Baldwin, Clinton T.;
Reardon, Annemarie F.;
Aiello, Alison;
Galea, Sandro;
Koenen, Karestan C.;
Uddin, Monica;
Wildman, Derek;
Miller, Mark W.

Publication type:

Article

Identification of Novel Candidate Genes for Alzheimer's Disease by Autozygosity Mapping using Genome Wide SNP Data.

Published in:

Journal of Alzheimer's Disease, 2011, v. 23, n. 2, p. 349, doi. 10.3233/JAD-2010-100714

By:

Sherva, Richard;
Baldwin, Clinton T.;
Inzelberg, Rivka;
Vardarajan, Badri;
Cupples, L. Adrienne;
Lunetta, Kathryn;
Bowirrat, Abdalla;
Naj, Adam;
Pericak-Vance, Margaret;
Friedland, Robert P.;
Farrer, Lindsay A.

Publication type:

Article

Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data.

Published in:

2011

By:

Sherva R;
Baldwin CT;
Inzelberg R;
Vardarajan B;
Cupples LA;
Lunetta K;
Bowirrat A;
Naj A;
Pericak-Vance M;
Friedland RP;
Farrer LA;
Sherva, Richard;
Baldwin, Clinton T;
Inzelberg, Rivka;
Vardarajan, Badri;
Cupples, L Adrienne;
Lunetta, Kathryn;
Bowirrat, Abdalla;
Naj, Adam;
Pericak-Vance, Margaret

Publication type:

journal article

A locus for autosomal recessive achromatopsia on human chromosome 8q.

Published in:

Clinical Genetics, 1999, v. 56, n. 1, p. 82, doi. 10.1034/j.1399-0004.1999.560112.x

By:

Milunsky, Aubrey;
Huang, Xin-Li;
Milunsky, Jeff;
DeStefano, Anita;
Baldwin, Clinton T

Publication type:

Article

A GENOME-WIDE ASSOCIATION STUDY OF CLINICAL SYMPTOMS OF DISSOCIATION IN A TRAUMA-EXPOSED SAMPLE.

Published in:

Depression & Anxiety (1091-4269), 2014, v. 31, n. 4, p. 352, doi. 10.1002/da.22260

By:

Wolf, Erika J.;
Rasmusson, Ann M.;
Mitchell, Karen S.;
Logue, Mark W.;
Baldwin, Clinton T.;
Miller, Mark W.

Publication type:

Article

Corticotropin releasing hormone receptor 2 (CRHR-2) gene is associated with decreased risk and severity of posttraumatic stress disorder in women.

Published in:

2013

By:

Wolf, Erika J;
Mitchell, Karen S;
Logue, Mark W;
Baldwin, Clinton T;
Reardon, Annemarie F;
Humphries, Donald E;
Miller, Mark W

Publication type:

journal article

CORTICOTROPIN RELEASING HORMONE RECEPTOR 2 ( CRHR-2) GENE IS ASSOCIATED WITH DECREASED RISK AND SEVERITY OF POSTTRAUMATIC STRESS DISORDER IN WOMEN.

Published in:

Depression & Anxiety (1091-4269), 2013, v. 30, n. 12, p. 1161, doi. 10.1002/da.22176

By:

Wolf, Erika J.;
Mitchell, Karen S.;
Logue, Mark W.;
Baldwin, Clinton T.;
Reardon, Annemarie F.;
Humphries, Donald E.;
Miller, Mark W.

Publication type:

Article

Diagnosis of Chronic Intestinal Pseudo-obstruction and Megacystis by Sequencing the ACTG2 Gene.

Published in:

2017

By:

Milunsky, Aubrey;
Baldwin, Clinton;
Xiaoying Zhang;
Primack, Daniel;
Curnow, Adrian;
Milunsky, Jeff;
Zhang, Xiaoying

Publication type:

journal article

Association of polymorphisms in the promoter region of the PNMT gene with essential hypertension in African Americans but not in whites

Published in:

American Journal of Hypertension, 2003, v. 16, n. 10, p. 859, doi. 10.1016/S0895-7061(03)01026-4

By:

Cui, Jing;
Zhou, Xiaofeng;
Chazaro, Irmarie;
DeStefano, Anita L.;
Manolis, Athanasios J.;
Baldwin, Clinton T.;
Gavras, Haralambos

Publication type:

Article

Identification of a polymorphic glutamic acid stretch in the α2b-adrenergic receptor and lack of linkage with essential hypertension.

Published in:

American Journal of Hypertension, 1999, v. 12, n. 9, p. 853, doi. 10.1016/S0895-7061(99)00070-9

By:

Baldwin, Clinton T.;
Schwartz, Faina;
Baima, Jader;
Burzstyn, Michael;
DeStefano, Anita L.;
Gavras, Irene;
Handy, Diane E.;
Joost, Oscar;
Martel, Timothy;
Manolis, Athanasios;
Nicolaou, Michael;
Bresnahan, Margaret;
Farrer, Lindsay;
Gavras, Haralambos

Publication type:

Article

Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF- β/BMP pathway.

Published in:

British Journal of Haematology, 2006, v. 133, n. 5, p. 570, doi. 10.1111/j.1365-2141.2006.06074.x

By:

Nolan, Vikki G.;
Adewoye, Adeboye;
Baldwin, Clinton;
Wang, Ling;
Ma, Qianli;
Wyszynski, Diego F.;
Farrell, John J.;
Sebastiani, Paola;
Farrer, Lindsay A.;
Steinberg, Martin H.

Publication type:

Article

Association of single nucleotide polymorphisms inklothowith priapism in sickle cell anaemia.

Published in:

British Journal of Haematology, 2005, v. 128, n. 2, p. 266, doi. 10.1111/j.1365-2141.2004.05295.x

By:

Nolan, Vikki G.;
Baldwin, Clinton;
Ma, Qianli;
Wyszynski, Diego F.;
Amirault, Yvonne;
Farrell, John J.;
Bisbee, Alice;
Embury, Stephen H.;
Farrer, Lindsay A.;
Steinberg, Martin H.

Publication type:

Article

Mutations in PAX3 associated with waardenburg syndrome type I.

Published in:

Human Mutation, 1994, v. 3, n. 3, p. 205, doi. 10.1002/humu.1380030306

By:

Baldwin, Clinton T.;
Lipsky, Nina R.;
Hoth, Christopher F.;
Cohen, Tirza;
Mamuya, Wilfred;
Milunsky, Aubrey

Publication type:

Article

Detection of sequence variants in the gene for human type II procollagen (COL2A1) by direct sequencing of polymerase chain reaction-amplified genomic DNA.

Published in:

Human Mutation, 1992, v. 1, n. 5, p. 403, doi. 10.1002/humu.1380010510

By:

Williams, Charlene J.;
Harrison, David A.;
Hopkinson, Ian;
Baldwin, Clinton T.;
Ahmad, N. Nina;
Ala-Kokko, Leena;
Korn, Richard M.;
Buxton, Paul G.;
Dimascio, Jeffrey;
Considine, Eileen L.;
Prockop, Darwin J.

Publication type:

Article

The genetics of hemoglobin A2 regulation in sickle cell anemia.

Published in:

American Journal of Hematology, 2014, v. 89, n. 11, p. 1019, doi. 10.1002/ajh.23811

By:

Griffin, Paula J.;
Sebastiani, Paola;
Edward, Heather;
Baldwin, Clinton T.;
Gladwin, Mark T.;
Gordeuk, Victor R.;
Chui, David H.K.;
Steinberg, Martin H.

Publication type:

Article

Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β0 thalassemia.

Published in:

American Journal of Hematology, 2013, v. 88, n. 6, p. 531, doi. 10.1002/ajh.23434

By:

Alsultan, Abdulrahman;
Ngo, Duyen;
Bae, Harold;
Sebastiani, Paola;
Baldwin, Clinton T.;
Melista, Efthymia;
Suliman, Ahmed M.;
Albuali, Waleed H.;
Nasserullah, Zaki;
Luo, Hong-yuan;
Chui, David H.K.;
Steinberg, Martin H.;
Al-Ali, Amein K.

Publication type:

Article

A functional promoter polymorphism of the δ-globin gene is a specific marker of the Arab-Indian haplotype.

Published in:

American Journal of Hematology, 2012, v. 87, n. 8, p. 824, doi. 10.1002/ajh.23239

By:

Alsultan, Abdulrahman;
Ngo, Duyen A.;
Farrell, John J.;
Akinsheye, Idowu;
Solovieff, Nadia;
Ghabbour, Hazem A.;
Al-Ali, Amein;
Alsuliman, Ahmed;
Al-Baghshi, Muneer;
Albu-Ali, Waleed;
Alabdulaali, Mohammed;
Baldwin, Clinton T.;
Farrer, Lindsay A.;
Luo, Hong;
Melista, Efthymia;
Safaya, Surinder;
Nwaru, Maxwell;
Chui, David H.K.;
Steinberg, Martin H.

Publication type:

Article

Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans.

Published in:

American Journal of Hematology, 2011, v. 86, n. 7, p. 612, doi. 10.1002/ajh.22032

By:

Alsultan, Abdulrahman;
Solovieff, Nadia;
Aleem, Aamer;
AlGahtani, Farjah H.;
Al-Shehri, Ali;
Elfaki Osman, Mohamed;
Kurban, Kadijah;
Bahakim, Hasan;
Kareem Al-Momen, Abdul;
Baldwin, Clinton T.;
Chui, David H.K.;
Steinberg, Martin H.

Publication type:

Article