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Publication Index
As in PubMed
As in Google Scholar
As in ResearcherID
Cheng YC, Anderson CD, Bione S, Keene K, Maguire JM, Nalls M, Rasheed A,
Zeginigg M, Attia J, Baker R, Barlera S, Biffi A, Bookman E, Brott TG,
Brown RD Jr, Chen F, Chen WM, Ciusani E, Cole JW, Cortellini L,
Danesh J, Doheny K, Ferrucci L, Grazia Franzosi M, Frossard P, Furie KL,
Golledge J, Hankey GJ, Hernandez D, Holliday EG, Hsu FC, Jannes J, Kamal
A, Khan MS, Kittner SJ, Koblar SA, Lewis M, Lincz L, Lisa A, Matarin M,
Moscato P, Mychaleckyj JC, Parati EA, Parolo S, Pugh E, Rost NS, Schallert
M, Schmidt H, Scott RJ, Sturm JW, Yadav S, Zaidi M, Boncoraglio GB, Levi
CR, Meschia JF, Rosand J, Sale M, Saleheen D, Schmidt R, Sharma P, Worrall
B, Mitchell BD; GARNET Collaborative Research Group; GENEVA Consortium;
International Stroke Genetics Consortium. (2012) Are myocardial
infarction-associated single-nucleotide polymorphisms associated with
ischemic stroke? Stroke 43(4):980-986
Manichaikul A, Palmas W, Rodriguez CJ, Peralta CA, Divers J, Guo X, Chen WM, Wong Q, Williams K, Kerr KF, Taylor KD, Tsai MY, Goodarzi MO, Sale MM, Diez-Roux AV, Rich SS,
Rotter JI, Mychaleckyj JC (2012) Population Structure of Hispanics in the United States: The Multi-Ethnic Study of Atherosclerosis. PLoS
Genet 8(4): e1002640 [PDF]
Manichaikul A, Chen WM, Williams K, Wong Q, Sale MM, Pankow JS,
Tsai MY, Rotter JI, Rich SS, Mychaleckyj JC. (2012) Analysis of family-
and population-based samples in cohort genome-wide association studies.
Hum Genet 131(2):275-287
Chen WM, Manichaikul A, Rich SS. (2011) Identifying variants
that contribute to linkage for dichotomous and quantitative traits in
extended pedigrees. BMC Proceedings 5(Suppl 9):S68 [PDF]
Chen WM, Allen EK, Mychaleckyj JC, Chen F, Hou X, Rich SS, Daly KA, Sale MM.
(2011) Fine mapping and further evaluation of linkage at chromosome 19q
for chronic otitis media with effusion and/or recurrent otitis media.
BMC Medical Genetics Sep 26;12:124
Sale MM, Chen WM, Weeks DE, Mychaleckyj JC, Hou X, Segade F, Casselbrant ML, Mandel EM, Ferrell RE, Rich SS, Daly KA.
(2011) Evaluation of 15 functional candidate genes for association with chronic otitis media with
effusion and/or recurrent otitis media (COME/ROM). PLoS ONE 6(8):e22297
Hsu FC, Sides E, Mychaleckyj J, Worrall BB, Elias G, Liu Y, Chen WM, Coull BM, Toole JF, Rich S, Furie KL, Sale MM. (2011) Transcobalamin 2
variant associated with post-stroke homocysteine modifies recurrent stroke
risk. Neurology 2011 Oct 18;77(16):1543-1550
Morahan G, Mehta M, James I, Chen WM, Akolkar B, Erlich HA, Hilner JE, Julier C, Nerup J,
Nierras C, Pociot F, Todd JA, Rich SS. (2011) Tests for genetic
interactions in type 1 diabetes: linkage and stratification analyses of
4,422 affected sib-pairs. Diabetes 60(3):1030-1040
Manichaikul A, Mychaleckyj JC, Rich SS, Daly K, Sale M, Chen WM
(2010) Robust relationship inference in genome-wide association studies.
Bioinformatics 26(22):2867-2873 [Abstract]
[PDF] [Software KING]
[Citation]
Terracciano A, Sanna S, Uda M, Deiana B, Usala G, Busonero F, Maschio A, Scally M, Patriciu N, Chen WM, Boomsma
DI,
Distel MA, Slagboom EP, Villafuerte S, Sliwerska E, Burmeister M, Amin N, Janssens AC, van Duijn CM , Schlessinger D,
Abecasis
G, Costa P (2010) Genome-wide association scan for five major dimensions
of personality. Mol Psychiatry 15(6):647-656 [PDF]
Divers J, Sale MM, Lu L, Chen WM, Lok KH, Spruill IJ, Fernandes
JK, Langefeld CD, Garvey WT (2010) The genetic architecture of lipoprotein
subclasses in Gullah-speaking
African American families enriched for type 2 diabetes: The Sea Islands
Genetic African American Registry (Project SuGAR). J Lipid Res
51:586-597 [PDF]
Chen WM, Manichaikul A, Rich SS (2009) A generalized
family-based association test for dichotomized traits. Am J Hum
Genet 85:364-376 [PDF] [Software]
Sale MM, Mychaleckyj JC, Chen WM (2009) Planning and executing a genome wide
association study (GWAS). Methods Mol Biol 590:403-418
[PDF]
Concannon P, Chen WM, Julier C, Morahan G, Akolkar B, Erlich HA, Hilner JE, Nerup J, Nierras C, Pociot F, Todd JA, Rich SS,and the
Type 1 Diabetes Genetics Consortium (2009) Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes
Genetics Consortium. Diabetes 58(4):1018-1022 [PDF]
Blackman JA, Gurka MJ, Bao Y, Dragulev BP, Chen WM, Romness MJ
(2009) Apolipoprotein E and functional motor severity in cerebral palsy.
J Pediatr Rehabil Med 2:67-74
Liang L, Chen WM, Sham PC, Abecasis GR (2009) Variance components linkage analysis with repeated measurements. Hum
Hered 67:237-247 [PDF]
Prokopenko I, Langenberg C, Florez JC, Saxena R, Soranzo N, Thorleifsson G, Loos RJ, Manning AK, Jackson AU, Aulchenko Y, Potter SC, Erdos MR, Sanna S, Hottenga JJ, Wheeler
E, Kaakinen M, Lyssenko V, Chen WM, Ahmadi K, Beckmann JS, Bergman RN, Bochud M, Bonnycastle LL, Buchanan TA, Cao A, Cervino A, Coin L, Collins FS, Crisponi L, de
Geus EJ,
Dehghan A, Deloukas P, Doney AS, Elliott P, Freimer N, Gateva V, Herder C, Hofman A, Hughes TE, Hunt S, Illig T, Inouye M, Isomaa B, Johnson T, Kong A, Krestyaninova M,
Kuusisto J, Laakso M, Lim N, Lindblad U, Lindgren CM, McCann OT, Mohlke KL, Morris AD, Naitza S, Orru M, Palmer CN, Pouta A, Randall J, Rathmann W, Saramies J, Scheet P,
Scott LJ, Scuteri A, Sharp S, Sijbrands E, Smit JH, Song K, Steinthorsdottir V, Stringham HM, Tuomi T, Tuomilehto J, Uitterlinden AG, Voight BF, Waterworth D, Wichmann HE,
Willemsen G, Witteman JC, Yuan X, Zhao JH, Zeggini E, Schlessinger D, Sandhu M, Boomsma DI, Uda M, Spector TD, Penninx BW, Altshuler D, Vollenweider P, Jarvelin MR, Lakatta
E, Waeber G, Fox CS, Peltonen L, Groop LC, Mooser V, Cupples LA, Thorsteinsdottir U, Boehnke M, Barroso I, Van Duijn C, Dupuis J, Watanabe RM, Stefansson K, McCarthy MI,
Wareham NJ, Meigs JB and Abecasis GR (2009) Variants in MTNR1B influence fasting glucose levels.
Nat Genet 41(1):77-81 [PDF]
Concannon P, Onengut-Gumuscu S, Todd JA, Smyth DJ, Pociot F, Bergholdt R, Akolkar B, Erlich HA, Hilner JE, Julier C,
Morahan G, Nerup J, Nierras CR, Chen WM, Rich SS; the Type 1 Diabetes Genetics Consortium (2008) A human type 1 diabetes susceptibility
locus maps to chromosome 21q22.3. Diabetes 57(10):2858-2861 [PDF]
Chen WM, Erdos MR, Jackson AU, Saxena R, Sanna S, Silver KD, Timpson NJ, Hansen T, Orru M, Grazia Piras M, Bonnycastle LL, Willer CJ, Lyssenko V, Shen H, Kuusisto J,
Ebrahim S, Sestu N, Duren WL, Spada MC, Stringham HM, Scott LJ, Olla N, Swift AJ, Najjar S, Mitchell BD, Lawlor DA, Smith GD, Ben-Shlomo Y, Andersen G, Borch-Johnsen K,
Jorgensen T, Saramies J, Valle TT, Buchanan TA, Shuldiner AR, Lakatta E, Bergman RN, Uda M, Tuomilehto J, Pedersen O, Cao A, Groop L, Mohlke KL, Laakso M, Schlessinger D,
Collins FS, Altshuler D, Abecasis GR, Boehnke M, Scuteri A and Watanabe RM (2008)
Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels.
J Clin Invest 118(7):2620-2628 [PDF]
[Citation]
Sanna S, Jackson AU, Nagaraja R, Willer CJ, Chen WM, Bonnycastle LL, Shen H, Timpson N,
Lettre G, Usala G, Chines PS, Stringham HM, Scott LJ, Dei M, Lai S, Albai G, Crisponi
L, Naitza S, Doheny KF, Pugh EW, Shlomo YB, Ebrahim S, Lawlor DA, Bergman RN,
Watanabe RM, Uda M, Tuomilehto J, Coresh J, Hirschhorn JN, Shuldiner AR, Schlessinger
D, Collins FS, Smith GD, Boerwinkle E, Cao A, Boehnke M, Abecasis GR, Mohlke KL
(2008) Common variants in the GDF5 - UQCC region are associated with variation in
human height. Nat Genet 40(2):198-203 [PDF]
Willer CJ, Sanna S, Jackson AU, Scuteri A, Bonnycastle LL, Clarke R, Heath SC, Timpson NJ, Najjar SS, Stringham HM,
Strait J, Duren WL, Maschio A, Busonero F, Mulas A, Albai G, Swift AJ, Morken MA, Narisu N, Bennett D, Parish S, Shen
H, Galan P, Meneton P, Hercberg S, Zelenika D, Chen WM, Li Y, Scott LJ, Scheet PA, Sundvall J, Watanabe RM, Nagaraja R, Ebrahim S,
Lawlor DA, Ben-Shlomo Y, Davey-Smith G, Shuldiner AR, Collins R, Bergman RN, Uda M, Tuomilehto J, Cao A, Collins FS, Lakatta
E, Lathrop GM, Boehnke M, Schlessinger D, Mohlke KL, Abecasis GR (2008) Newly identified loci that influence lipid concentrations and risk of coronary artery disease.
Nat Genet 40(2):161-169 [PDF]
Uda M, Galanello R, Sanna S, Lettre G, Sankaran VG, Chen W, Usala G, Busonero F, Maschio A, Albai G, Piras MG, Sestu N, Lai S, Dei
M, Mulas A, Crisponi L, Naitza S, Asunis I, Deiana M, Nagaraja R, Perseu L, Satta S, Cipollina MD, Sollaino C, Moi P, Hirschhorn JN, Orkin
SH, Abecasis GR, Schlessinger D, Cao A (2008) Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and
amelioration of the phenotype of beta-thalassemia. Proc Natl Acad Sci 105(5):1620-1625 [PDF]
Li S, Sanna S, Maschio A, Busonero F, Usala G, Mulas A, Lai S, Dei M, Orru M, Albai G, Bandinelli S, Schlessinger D, Lakatta E, Scuteri A, Najjar SS, Jack G,
Naitza S, Crisponi L, Cao A, Abecasis GR, Ferrucci L, Uda M, Chen WM, Nagaraja1 R (2007)
The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti Cohorts.
PLoS Genet 3(11):e194 [PDF]
Chen WM, Abecasis GR (2007) Family-based association tests for genomewide association scans. Am J Hum Genet
81:913-926
[Abstract]
[PDF]
[Citation]
Scuteri A, Sanna S, Chen WM, Uda M, Albai G, Strait J, Najjar S, Nagaraja R, Orru M, Usala G, Dei M, Lai S, Maschio A, Busonero F,
Mulas A, Ehret GB, Fink AA, Weder AB, Cooper RS, Galan P, Chakravarti A, Schlessinger D, Cao A, Lakatta E, Abecasis GR (2007)
Genome wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. PLoS Genet 3(7):e115 [PDF]
Burdick JT, Chen WM, Abecasis GR, Cheung VG (2006) In silico
method for inferring genotypes in pedigrees. Nat Genet 38:1002-4 [PDF]
[Citation]
Pilia G, Chen WM, et al. (2006) Heritability of cardiovascular and personality traits in 6,148 Sardinians.
PLoS Genet 2(8):e132 [PDF]
Chen WM, Abecasis GR (2006) Estimating the power of variance component linkage analysis in large pedigrees. Genet
Epidemiol 30:471-84 [PDF]
[Citation]
Chen WM, Broman KW and Liang KY
(2005).
Power and robustness of linkage tests for quantitative traits in general pedigrees.
Genet Epidemiol 28:11-23
[Abstract]
[PDF]
[Citation]
Chen WM, Broman KW and Liang KY
(2004).
Quantitative trait linkage analysis by generalized estimating equations: unification of variance components and Haseman-Elston regression.
Genet Epidemiol 26:265-72
[Abstract]
[PDF]
[Citation]
Fallin D, Beaty T, Liang KY and Chen W
(2002).
"Power comparisons for genotypic vs. allelic TDT methods with >2 alleles".
Genet Epidemiol 23:458-61; author reply 462-4
[PDF]
Deng HW, Chen WM and Recker RR
(2002).
Transmission disequilibrium test with discordant sib pairs when parents are available.
Hum Genet 110:451-61
[Abstract]
[PDF]
Chen WM and Deng HW
(2001).
A general and accurate approach for computing the statistical power of the transmission disequilibrium test for
complex disease genes.
Genet Epidemiol 21:53-67
[Abstract]
[PDF]
[Citation]
[Software]
Deng HW and Chen WM
(2001).
The power of the transmission disequilibrium test (TDT) with both case-parent and control-parent trios.
Genet Res 78:289-302
[Abstract]
[PDF]
Deng HW, Chen WM and Recker RR
(2001).
Population admixture: detection by Hardy-Weinberg test and its quantitative effects on linkage-disequilibrium methods for localizing genes underlying complex traits.
Genetics 157:885-97
[Abstract]
[PDF]
Deng HW, Chen WM, Conway T, Zhou Y, Davies KM, Stegman MR, Deng H and Recker RR
(2000).
Determination of bone mineral density of the hip and spine in human pedigrees by genetic and life-style factors.
Genet Epidemiol 19:160-77
[Abstract]
[PDF]
Deng HW, Chen WM, Recker S, Stegman MR, Li JL, Davies KM, Zhou Y, Deng H, Heaney R and Recker RR
(2000).
Genetic determination of Colles' fracture and differential bone mass in women with and without Colles' fracture.
J Bone Miner Res 15:1243-52
[Abstract]
[PDF]
Deng HW, Chen WM and Recker RR
(2000).
QTL fine mapping by measuring and testing for Hardy-Weinberg and linkage disequilibrium at a series of linked marker loci in extreme samples of populations.
Am J Hum Genet 66:1027-45
[Abstract]
[PDF]
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