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KAO, WEN

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Publications

  • 1.

    2009

    Malhotra Alka; Igo Robert P; Thameem Farook; Kao W H Linda; Abboud Hanna E; Adler Sharon G; Arar Nedal H; Bowden Donald W; Duggirala Ravindranath; Freedman Barry I; Goddard Katrina A B; Ipp Eli; Iyengar Sudha K; Kimmel Paul L; Knowler William C; Kohn Orly; Leehey David; Meoni Lucy A; Nelson Robert G; Nicholas Susanne B; Parekh Rulan S; Rich Stephen S; Chen Yii-Der I; Saad Mohammed F; Scavini Marina; Schelling Jeffrey R; Sedor John R; Shah Vallabh O; Taylor Kent D; Thornley-Brown Denyse; Zager Philip G; Horvath Amanda; Hanson Robert L;

    Genome-wide linkage scans for type 2 diabetes mellitus in four ethnically diverse populations-significant evidence for linkage on chromosome 4q in African Americans: the family investigation of nephropathy and diabetes research group.

    Diabetes/metabolism research and reviews 2009;25(8):740-7.

  • 2.

    2009

    Naj Adam C; Kao Wen-Hong L; O'Connell Jeffrey R; Mitchell Braxton D; Silver Kristi D

    Sequence variation in IGF1R is associated with differences in insulin levels in nondiabetic old order Amish.

    Diabetes/metabolism research and reviews 2009;25(8):773-9.

  • 3.

    2009

    Benjamin Emelia J; Rice Kenneth M; Arking Dan E; Pfeufer Arne; van Noord Charlotte; Smith Albert V; Schnabel Renate B; Bis Joshua C; Boerwinkle Eric; Sinner Moritz F; Dehghan Abbas; Lubitz Steven A; D'Agostino Ralph B; Lumley Thomas; Ehret Georg B; Heeringa Jan; Aspelund Thor; Newton-Cheh Christopher; Larson Martin G; Marciante Kristin D; Soliman Elsayed Z; Rivadeneira Fernando; Wang Thomas J; Eiríksdottir Gudny; Levy Daniel; Psaty Bruce M; Li Man; Chamberlain Alanna M; Hofman Albert; Vasan Ramachandran S; Harris Tamara B; Rotter Jerome I; Kao W H Linda; Agarwal Sunil K; Stricker Bruno H Ch; Wang Ke; Launer Lenore J; Smith Nicholas L; Chakravarti Aravinda; Uitterlinden André G; Wolf Philip A; Sotoodehnia Nona; Köttgen Anna; van Duijn Cornelia M; Meitinger Thomas; Mueller Martina; Perz Siegfried; Steinbeck Gerhard; Wichmann H-Erich; Lunetta Kathryn L; Heckbert Susan R; Gudnason Vilmundur; Alonso Alvaro; Kääb Stefan; Ellinor Patrick T; Witteman Jacqueline C M

    Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.

    Nature genetics 2009;41(8):879-81.

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Most Frequent Journals

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    Publications
  • Diabetes care
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  • Diabetes
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  • Journal of the American S...
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  • Nature genetics
    4
  • American journal of kidne...
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