Publications

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A
Weinstock JS, Gopakumar J, Burugula BBharathi, Uddin MMesbah, Jahn N, Belk JA, Bouzid H, Daniel B, Miao Z, Ly N et al..  2023.  Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.. Nature. 616(7958):755-763.
Bressler J, Davies G, Smith AV, Saba Y, Bis JC, Jian X, Hayward C, Yanek L, Smith JA, Mirza SS et al..  2021.  Association of low-frequency and rare coding variants with information processing speed.. Transl Psychiatry. 11(1):613.
Zhang Y, Liu X, Wiggins KL, Kurniansyah N, Guo X, Rodrigue AL, Zhao W, Yanek LR, Ratliff SM, Pitsillides A et al..  2023.  Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function: A Meta-analysis of Community-Based Cohorts.. Neurology. 100(18):e1930-e1943.
Bick AG, Weinstock JS, Nandakumar SK, Fulco CP, Bao EL, Zekavat SM, Szeto MD, Liao X, Leventhal MJ, Nasser J et al..  2021.  Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes.. Nature. 591(7851):E27.
Davies G, Lam M, Harris SE, Trampush JW, Luciano M, W Hill D, Hagenaars SP, Ritchie SJ, Marioni RE, Fawns-Ritchie C et al..  2019.  Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.. Nat Commun. 10(1):2068.
C
Natarajan P, Pampana A, Graham SE, Ruotsalainen SE, Perry JA, de Vries PS, Broome JG, Pirruccello JP, Honigberg MC, Aragam K et al..  2021.  Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.. Nat Commun. 12(1):2182.
Bressler J, Davies G, Smith AV, Saba Y, Bis JC, Jian X, Hayward C, Yanek L, Smith JA, Mirza SS et al..  2022.  Correction: Association of low-frequency and rare coding variants with information processing speed.. Transl Psychiatry. 12(1):88.
D
Surendran P, Feofanova EV, Lahrouchi N, Ntalla I, Karthikeyan S, Cook J, Chen L, Mifsud B, Yao C, Kraja AT et al..  2020.  Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.. Nat Genet. 52(12):1314-1332.
Ward-Caviness CK, Huffman JE, Everett K, Germain M, van Dongen J, W Hill D, Jhun MA, Brody JA, Ghanbari M, Du L et al..  2018.  DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis.. Blood. 132(17):1842-1850.
Richard MA, Huan T, Ligthart S, Gondalia R, Jhun MA, Brody JA, Irvin MR, Marioni R, Shen J, Tsai P-C et al..  2017.  DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation.. Am J Hum Genet. 101(6):888-902.
Li X, Li Z, Zhou H, Gaynor SM, Liu Y, Chen H, Sun R, Dey R, Arnett DK, Aslibekyan S et al..  2020.  Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.. Nat Genet. 52(9):969-983.
E
Yang Y, Knol MJ, Wang R, Mishra A, Liu D, Luciano M, Teumer A, Armstrong N, Bis JC, Jhun MA et al..  2023.  Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI.. Brain. 146(2):492-506.
Morrison AC, Brown A, Kardia SLR, Turner ST, Boerwinkle E.  2003.  Evaluating the context-dependent effect of family history of stroke in a genome scan for hypertension.. Stroke. 34(5):1170-5.
F
Fornage M, Mosley TH, Jack CR, de Andrade M, Kardia SLR, Boerwinkle E, Turner ST.  2007.  Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury.. Hum Genet. 120(5):671-80.
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Fuentes Lde Las, Sung YJu, Noordam R, Winkler T, Feitosa MF, Schwander K, Bentley AR, Brown MR, Guo X, Manning A et al..  2021.  Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.. Mol Psychiatry. 26(6):2111-2125.
Fuentes Lde Las, Schwander KL, Brown MR, Bentley AR, Winkler TW, Sung YJu, Munroe PB, Miller CL, Aschard H, Aslibekyan S et al..  2023.  Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.. Front Genet. 14:1235337.
Lahti J, Tuominen S, Yang Q, Pergola G, Ahmad S, Amin N, Armstrong NJ, Beiser A, Bey K, Bis JC et al..  2022.  Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning.. Mol Psychiatry. 27(11):4419-4431.
I
Bick AG, Weinstock JS, Nandakumar SK, Fulco CP, Bao EL, Zekavat SM, Szeto MD, Liao X, Leventhal MJ, Nasser J et al..  2020.  Inherited causes of clonal haematopoiesis in 97,691 whole genomes.. Nature. 586(7831):763-768.
Kelly TN, Sun X, He KY, Brown MR, Taliun SAGagliano, Hellwege JN, Irvin MR, Mi X, Brody JA, Franceschini N et al..  2022.  Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.. Hypertension. 79(8):1656-1667.
L
Day FR, Ruth KS, Thompson DJ, Lunetta KL, Pervjakova N, Chasman DI, Stolk L, Finucane HK, Sulem P, Bulik-Sullivan B et al..  2015.  Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.. Nat Genet. 47(11):1294-1303.
He KY, Li X, Kelly TN, Liang J, Cade BE, Assimes TL, Becker LC, Beitelshees AL, Bress AP, Chang Y-PChristy et al..  2019.  Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data.. Hum Genet. 138(2):199-210.
M
Ward-Caviness CK, de Vries PS, Wiggins KL, Huffman JE, Yanek LR, Bielak LF, Giulianini F, Guo X, Kleber ME, Kacprowski T et al..  2019.  Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease.. PLoS One. 14(5):e0216222.
Sun D, Richard M, Musani SK, Sung YJu, Winkler TW, Schwander K, Chai JFang, Guo X, Kilpeläinen TO, Vojinovic D et al..  2021.  Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits.. HGG Adv. 2(1)
de Vries PS, Brown MR, Bentley AR, Sung YJ, Winkler TW, Ntalla I, Schwander K, Kraja AT, Guo X, Franceschini N et al..  2019.  Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.. Am J Epidemiol. 188(6):1033-1054.
Bentley AR, Sung YJ, Brown MR, Winkler TW, Kraja AT, Ntalla I, Schwander K, Chasman DI, Lim E, Deng X et al..  2019.  Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.. Nat Genet. 51(4):636-648.