Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study von Carty, C.L., Spencer, K.L., Setiawan, V.W., Fernandez-Rhodes, L., Malinowski, J., Buyske, S., Young, A., Jorgensen, N.W., Cheng, I., Carlson, C.S., Brown-Gentry, K., Goodloe, R., Park, A., Parikh, N.I., Henderson, B., Le Marchand, L., Wactawski-Wende, J., Fornage, M., Matise, T.C., Hindorff, L.A., Arnold, A.M., Haiman, C.A., Franceschini, N., Peters, U., Crawford, D.C.

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Common VKORC1 variants are not associated with arterial or venous thrombosis von HINDORFF, L. A., HECKBERT, S. R., SMITH, N., MARCIANTE, K. D., PSATY, B. M.

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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits von Hindorff, Lucia A, Sethupathy, Praveen, Junkins, Heather A, Ramos, Erin M, Mehta, Jayashri P, Collins, Francis S, Manolio, Teri A

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Genetic determinants of age-related macular degeneration in diverse populations from the PAGE study von Restrepo, Nicole A, Spencer, Kylee L, Goodloe, Robert, Garrett, Tiana A, Heiss, Gerardo, Bůžková, Petra, Jorgensen, Neal, Jensen, Richard A, Matise, Tara C, Hindorff, Lucia A, Klein, Barbara E K, Klein, Ronald, Wong, Tien Y, Cheng, Ching-Yu, Cornes, Belinda K, Tai, E-Shyong, Ritchie, Marylyn D, Haines, Jonathan L, Crawford, Dana C

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The use of phenome-wide association studies (PheWAS) for exploration of novel genotype-phenotype relationships and pleiotropy discovery von Pendergrass, S.A., Brown-Gentry, K., Dudek, S.M., Torstenson, E.S., Ambite, J.L., Avery, C.L., Buyske, S., Cai, C., Fesinmeyer, M.D., Haiman, C., Heiss, G., Hindorff, L.A., Hsu, C.-N., Jackson, R.D., Kooperberg, C., Le Marchand, L., Lin, Y., Matise, T.C., Moreland, L., Monroe, K., Reiner, A.P., Wallace, R., Wilkens, L.R., Crawford, D.C., Ritchie, M.D.

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Polymorphisms of coagulation factor XIII subunit A and risk of nonfatal hemorrhagic stroke in young white women von Reiner, A P, Schwartz, S M, Frank, M B, Longstreth, Jr, W T, Hindorff, L A, Teramura, G, Rosendaal, F R, Gaur, L K, Psaty, B M, Siscovick, D S

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Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations von Yoneyama, S, Yao, J, Guo, X, Fernandez-Rhodes, L, Lim, U, Boston, J, Buzková, P, Carlson, C S, Cheng, I, Cochran, B, Cooper, R, Ehret, G, Fornage, M, Gong, J, Gross, M, Gu, C C, Haessler, J, Haiman, C A, Henderson, B, Hindorff, L A, Houston, D, Irvin, M R, Jackson, R, Kuller, L, Leppert, M, Lewis, C E, Li, R, Le Marchand, L, Matise, T C, Nguyen, K-DH, Chakravarti, A, Pankow, J S, Pankratz, N, Pooler, L, Ritchie, M D, Bien, S A, Wassel, C L, Chen, Y-DI, Taylor, K D, Allison, M, Rotter, J I, Schreiner, P J, Schumacher, F, Wilkens, L, Boerwinkle, E, Kooperberg, C, Peters, U, Buyske, S, Graff, M, North, K E

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Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI von Gong, J, Nishimura, K K, Fernandez-Rhodes, L, Haessler, J, Bien, S, Graff, M, Lim, U, Lu, Y, Gross, M, Fornage, M, Yoneyama, S, Isasi, C R, Buzkova, P, Daviglus, M, Lin, D-Y, Tao, R, Goodloe, R, Bush, W S, Farber-Eger, E, Boston, J, Dilks, H H, Ehret, G, Gu, C C, Lewis, C E, Nguyen, K-D H, Cooper, R, Leppert, M, Irvin, M R, Bottinger, E P, Wilkens, L R, Haiman, C A, Park, L, Monroe, K R, Cheng, I, Stram, D O, Carlson, C S, Jackson, R, Kuller, L, Houston, D, Kooperberg, C, Buyske, S, Hindorff, L A, Crawford, D C, Loos, R J F, Le Marchand, L, Matise, T C, North, K E, Peters, U

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Family history of diabetes as a potential public health tool von Harrison, Tabitha A, Hindorff, Lucia A, Kim, Helen, Wines, Roberta C.M, Bowen, Deborah J, McGrath, Barbara B, Edwards, Karen L

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Expression of a Cloned Cyclopropane Fatty Acid Synthase Gene Reduces Solvent Formation in Clostridium acetobutylicum ATCC 824 von YINSUO ZHAO, HINDORFF, Lucia A, CHUANG, Amy, MONROE-AUGUSTUS, Melanie, LYRISTIS, Michael, HARRISON, Mary L, RUDOLPH, Frederick B, BENNETT, George N

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Use of Factor V Leiden genetic testing in practice and impact on management von Laberge, Anne-Marie, Psaty, Bruce M, Hindorff, Lucia A, Burke, Wylie

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Angiotensin II type 1 receptor polymorphisms in the cardiovascular health study: relation to blood pressure, ethnicity, and cardiovascular events von Hindorff, Lucia A, Heckbert, Susan R, Tracy, Russell, Tang, Zhonghua, Psaty, Bruce M, Edwards, Karen L, Siscovick, David S, Kronmal, Richard A, Nazar-Stewart, Valle

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1- and  2-Adrenergic Receptor Gene Variation,  -Blocker Use and Risk of Myocardial Infarction and Stroke von Lemaitre, R. N., Heckbert, S. R., Sotoodehnia, N., Bis, J. C., Smith, N. L., Marciante, K. D., Hindorff, L. A., Lange, L. A., Lumley, T. S., Rice, K. M., Wiggins, K. L., Psaty, B. M.

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Genetic risk factors for body mass index and obesity in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemiology (PAGE) Study von Fesinmeyer, MD, North, KE, Ritchie, MD, Lim, U, Franceschini, N, Wilkens, LR, Gross, MD, Bůžková, P, Glenn, K, Quibrera, PM, Fernández-Rhodes, L, Li, Q, Fowke, JH, Li, R, Carlson, CS, Prentice, RL, Kuller, LH, Manson, JE, Matise, TC, Cole, SA, Chen, CTL, Howard, BV, Kolonel, LN, Henderson, BE, Monroe, KR, Crawford, DC, Hindorff, LA, Buyske, S, Haiman, CA, Le Marchand, L, Peters, U

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Genetic variants of coagulation factor XIII, postmenopausal estrogen therapy, and risk of nonfatal myocardial infarction von Reiner, Alexander P., Heckbert, Susan R., Vos, Hans L., Ariëns, Robert A.S., Lemaitre, Rozenn N., Smith, Nicholas L., Lumley, Thomas, Rea, Thomas D., Hindorff, Lucia A., Schellenbaum, Gina D., Rosendaal, Frits R., Siscovick, David S., Psaty, Bruce M.

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Genetic risk factors for body mass index and obesity in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemiology (PAGE) Study von Fesinmeyer, MD, North, KE, Ritchie, MD, Lim, U, Franceschini, N, Wilkens, LR, Gross, MD, Bůžková, P, Glenn, K, Quibrera, PM, Fernández-Rhodes, L, Li, Q, Fowke, JH, Li, R, Carlson, CS, Prentice, RL, Kuller, LH, Manson, JE, Matise, TC, Cole, SA, Chen, CTL, Howard, BV, Kolonel, LN, Henderson, BE, Monroe, KR, Crawford, DC, Hindorff, LA, Buyske, S, Haiman, CA, Le Marchand, L, Peters, U

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Common Genetic Variation in the Prothrombin Gene, Hormone Therapy, and Incident Nonfatal Myocardial Infarction in Postmenopausal Women von Hindorff, Lucia A., Psaty, Bruce M., Carlson, Christopher S., Heckbert, Susan R., Lumley, Thomas, Smith, Nicholas L., Lemaitre, Rozenn N., Rieder, Mark J., Nickerson, Deborah A., Reiner, Alexander P.

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Beta2-adrenergic receptor polymorphisms and risk of incident cardiovascular events in the elderly von Heckbert, Susan R, Hindorff, Lucia A, Edwards, Karen L, Psaty, Bruce M, Lumley, Thomas, Siscovick, David S, Tang, Zhonghua, Durda, J Peter, Kronmal, Richard A, Tracy, Russell P

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Polymorphisms of Coagulation Factor XIII Subunit A and Risk of Nonfatal Hemorrhagic Stroke in Young White Women Editorial Comment von Reiner, A. P., Schwartz, S. M., Frank, M. B., Longstreth, W.T., Hindorff, L. A., Teramura, G., Rosendaal, F. R., Gaur, L. K., Psaty, B. M., Siscovick, D. S., Leclerc, J. R.

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The Association of PAI-1 Promoter 4G/5G Insertion/Deletion Polymorphism with Myocardial Infarction and Stroke in Young Women von Hindorff, Lucia A., Schwartz, Stephen M., Siscovick, David S., Psaty, Bruce M., Longstreth, W.T., Reiner, Alexander P.

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