A DNA methylation biomarker of alcohol consumption
Liu, C, Marioni, R E, Hedman, Å K, Pfeiffer, L, Tsai, P-C, Reynolds, L M, Just, A C, Duan, Q, Boer, C G, Tanaka, T, Elks, C E, Aslibekyan, S, Brody, J A, Kühnel, B, Herder, C, Almli, L M, Zhi, D, Wang, Y, Huan, T, Yao, C, Mendelson, M M, Joehanes, R, Liang, L, Love, S-A, Guan, W, Shah, S, McRae, A F, Kretschmer, A, Prokisch, H, Strauch, K, Peters, A, Visscher, P M, Wray, N R, Guo, X, Wiggins, K L, Smith, A K, Binder, E B, Ressler, K J, Irvin, M R, Absher, D M, Hernandez, D, Ferrucci, L, Bandinelli, S, Lohman, K, Ding, J, Trevisi, L, Gustafsson, S, Sandling, J H, Stolk, L, Uitterlinden, A G, Yet, I, Castillo-Fernandez, J E, Spector, T D, Schwartz, J D, Vokonas, P, Lind, L, Li, Y, Fornage, M, Arnett, D K, Wareham, N J, Sotoodehnia, N, Ong, K K, van Meurs, J B J, Conneely, K N, Baccarelli, A A, Deary, I J, Bell, J T, North, K E, Liu, Y, Waldenberger, M, London, S J, Ingelsson, E, Levy, D
Published in Molecular psychiatry (01.02.2018)
Published in Molecular psychiatry (01.02.2018)
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Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat
Sung, Y J, Pérusse, L, Sarzynski, M A, Fornage, M, Sidney, S, Sternfeld, B, Rice, T, Terry, J G, Jacobs, Jr, D R, Katzmarzyk, P, Curran, J E, Jeffrey Carr, J, Blangero, J, Ghosh, S, Després, J-P, Rankinen, T, Rao, D C, Bouchard, C
Published in International Journal of Obesity (01.04.2016)
Published in International Journal of Obesity (01.04.2016)
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A genotype risk score predicts type 2 diabetes from young adulthood: the CARDIA study
Vassy, J. L., Durant, N. H., Kabagambe, E. K., Carnethon, M. R., Rasmussen-Torvik, L. J., Fornage, M., Lewis, C. E., Siscovick, D. S., Meigs, J. B.
Published in Diabetologia (01.10.2012)
Published in Diabetologia (01.10.2012)
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Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease
Schmidt, Helena, Zeginigg, Marion, Wiltgen, Marco, Freudenberger, Paul, Petrovic, Katja, Cavalieri, Margherita, Gider, Pierre, Enzinger, Christian, Fornage, Myriam, Debette, Stephanie, Rotter, Jerome I., Ikram, Mohammad A., Launer, Lenore J., Schmidt, Reinhold
Published in Brain (London, England : 1878) (01.11.2011)
Published in Brain (London, England : 1878) (01.11.2011)
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The Alzheimer's Disease Sequencing Project: Study design and sample selection
Beecham, Gary W, Bis, J C, Martin, E R, Choi, S-H, DeStefano, A L, van Duijn, C M, Fornage, M, Gabriel, S B, Koboldt, D C, Larson, D E, Naj, A C, Psaty, B M, Salerno, W, Bush, W S, Foroud, T M, Wijsman, E, Farrer, L A, Goate, A, Haines, J L, Pericak-Vance, Margaret A, Boerwinkle, E, Mayeux, R, Seshadri, S, Schellenberg, G
Published in Neurology. Genetics (01.10.2017)
Published in Neurology. Genetics (01.10.2017)
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Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study
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.
Published in Human reproduction (Oxford) (01.06.2013)
Published in Human reproduction (Oxford) (01.06.2013)
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Association of 25-Hydroxyvitamin D status and genetic variation in the vitamin D metabolic pathway with FEV1 in the Framingham Heart Study
Hansen, J G, Gao, W, Dupuis, J, O'Connor, G T, Tang, W, Kowgier, M, Sood, A, Gharib, S A, Palmer, L J, Fornage, M, Heckbert, S R, Psaty, B M, Booth, S L, Cassano, Patricia A
Published in Respiratory research (01.07.2015)
Published in Respiratory research (01.07.2015)
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Association of coagulation‐related and inflammation‐related genes and factor VIIc levels with stroke: the Cardiovascular Health Study
ZAKAI, N. A., LANGE, L., LONGSTRETH, W. T., O’MEARA, E. S., KELLEY, J. L., FORNAGE, M., NIKERSON, D., CUSHMAN, M., REINER, A. P.
Published in Journal of thrombosis and haemostasis (01.02.2011)
Published in Journal of thrombosis and haemostasis (01.02.2011)
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SNP-by-fitness and SNP-by-BMI interactions from seven candidate genes and incident hypertension after 20 years of follow-up: the CARDIA Fitness Study
SARZYNSKI, M. A, RANKINEN, T, STERNFELD, B, FORNAGE, M, SIDNEY, S, BOUCHARD, C
Published in Journal of human hypertension (01.08.2011)
Published in Journal of human hypertension (01.08.2011)
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Association between patterns of nucleotide variation across the three fibrinogen genes and plasma fibrinogen levels: the Coronary Artery Risk Development in Young Adults (CARDIA) study
REINER, A. P., CARTY, C. L., CARLSON, C. S., WAN, J. Y., RIEDER, M. J., SMITH, J. D., RICE, K., FORNAGE, M., JAQUISH, C. E., WILLIAMS, O. D., TRACY, R. P., LEWIS, C. E., SISCOVICK, D. S., BOERWINKLE, E., NICKERSON, D. A.
Published in Journal of thrombosis and haemostasis (01.06.2006)
Published in Journal of thrombosis and haemostasis (01.06.2006)
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Lack of association between a biallelic polymorphism in the adducin gene and blood pressure in whites and African Americans
Schork, Nicholas J, Chakravarti, Aravinda, Thiel, Bonnie, Fornage, Myriam, Jacob, Howard J, Cai, Robin, Rotimi, Charles N, Cooper, Richard S, Weder, Alan B
Published in American journal of hypertension (01.06.2000)
Published in American journal of hypertension (01.06.2000)
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Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation
Longchamps, R. J., Yang, S. Y., Castellani, C. A., Shi, W., Lane, J., Grove, M. L., Bartz, T. M., Sarnowski, C., Liu, C., Burrows, K., Guyatt, A. L., Gaunt, T. R., Kacprowski, T., Yang, J., De Jager, P. L., Yu, L., Bergman, A., Xia, R., Fornage, M., Feitosa, M. F., Wojczynski, M. K., Kraja, A. T., Province, M. A., Amin, N., Rivadeneira, F., Tiemeier, H., Uitterlinden, A. G., Broer, L., Van Meurs, J. B. J., Van Duijn, C. M., Raffield, L. M., Lange, L., Rich, S. S., Lemaitre, R. N., Goodarzi, M. O., Sitlani, C. M., Mak, A. C. Y., Bennett, D. A., Rodriguez, S., Murabito, J. M., Lunetta, K. L., Sotoodehnia, N., Atzmon, G., Ye, K., Barzilai, N., Brody, J. A., Psaty, B. M., Taylor, K. D., Rotter, J. I., Boerwinkle, E., Pankratz, N., Arking, D. E.
Published in Human genetics (01.01.2022)
Published in Human genetics (01.01.2022)
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Circulating Metabolome and White Matter Hyperintensities in Women and Men
Sliz, Eeva, Shin, Jean, Ahmad, Shahzad, Williams, Dylan M, Frenzel, Stefan, Gauß, Friederike, Harris, Sarah E, Henning, Ann-Kristin, Hernandez, Maria Valdes, Hu, Yi-Han, Jiménez, Beatriz, Sargurupremraj, Muralidharan, Sudre, Carole, Wang, Ruiqi, Wittfeld, Katharina, Yang, Qiong, Wardlaw, Joanna M, Völzke, Henry, Vernooij, Meike W, Schott, Jonathan M, Richards, Marcus, Proitsi, Petroula, Nauck, Matthias, Lewis, Matthew R, Launer, Lenore, Hosten, Norbert, Grabe, Hans J, Ghanbari, Mohsen, Deary, Ian J, Cox, Simon R, Chaturvedi, Nishi, Barnes, Josephine, Rotter, Jerome I, Debette, Stephanie, Ikram, M Arfan, Fornage, Myriam, Paus, Tomas, Seshadri, Sudha, Pausova, Zdenka
Published in Circulation (New York, N.Y.) (05.04.2022)
Published in Circulation (New York, N.Y.) (05.04.2022)
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A Mendelian randomization of gamma' and total fibrinogen levels in relation to venous thromboembolism and ischemic stroke: Blood
Maners, J., Gill, D., Pankratz, N., Laffan, M. A., Wolberg, A. S., de Maat, M. P. M., Ligthart, S., Tang, W., Ward-Caviness, C. K., Fornage, M., Debette, Stephanie, Dichgans, M., Mcknight, B., Boerwinkle, E., Smith, N. L., Morrison, A. C., Dehghan, A., de Vries, P. S.
Published in Blood (24.12.2020)
Published in Blood (24.12.2020)
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Genome-Wide Association Studies of Cerebral White Matter Lesion Burden: The CHARGE Consortium
FORNAGE, Myriam, DEBETTE, Stephanie, VROOMAN, Henri A, SHIBATA, Dean K, MAILLARD, Pauline, ZIJDENBOS, Alex, SMITH, Albert V, GUDNASON, Haukur, DE BOER, Renske, CUSHMAN, Mary, MAZOYER, Bernard, HEISS, Gerardo, BIS, Joshua C, VERNOOIJ, Meike W, ENZINGER, Christian, GLAZER, Nicole L, BEISER, Alexa, KNOPMAN, David S, CAVALIERI, Margherita, NIESSEN, WiroJ, HARRIS, TamaraB, PETROVIC, Katja, LOPEZ, Oscar L, SCHMIDT, Helena, AU, Rhoda, LAMBERT, Jean-Charles, HOFMAN, Albert, GOTTESMAN, Rebecca F, GARCIA, Melissa, HECKBERT, SusanR, ATWOOD, LarryD, CATELLIER, DianeJ, UITTERLINDEN, Andre G, QIONG YANG, ARFAN IKRAM, M, SMITH, Nicholas L, ASPELUND, Thor, ROMERO, Jose R, RICE, Kenneth, TAYLOR, Kent D, NALLS, Michael A, ROTTER, Jerome I, SHARRETT, Richey, VAN DUIJN, Cornelia M, AMOUYEL, Philippe, DUFOUIL, Carole, WOLF, Philip A, GUDNASON, Vilmundur, VAN DER LUGT, Aad, BOERWINKLE, Eric, PSATY, Bruce M, SESHADRI, Sudha, TZOURIO, Christophe, BRETELER, Monique M. B, MOSLEY, Thomas H, SCHMIDT, Reinhold, SIGURDSSON, Sigurdur, LUMLEY, Thomas, DESTEFANO, Anita L, FAZEKAS, Franz
Published in Annals of neurology (01.06.2011)
Published in Annals of neurology (01.06.2011)
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A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology
de Vries, Paul S., Sabater-Lleal, Maria, Huffman, Jennifer E., Marten, Jonathan, Song, Ci, Pankratz, Nathan, Bartz, Traci M., de Haan, Hugoline G., Delgado, Graciela E., Eicher, John D., Martinez-Perez, Angel, Ward-Caviness, Cavin K., Brody, Jennifer A., Chen, Ming-Huei, de Maat, Moniek P.M., Frånberg, Mattias, Gill, Dipender, Kleber, Marcus E., Rivadeneira, Fernando, Soria, José Manuel, Tang, Weihong, Tofler, Geoffrey H., Uitterlinden, André G., van Hylckama Vlieg, Astrid, Seshadri, Sudha, Boerwinkle, Eric, Davies, Neil M., Giese, Anne-Katrin, Ikram, M. Kamran, Kittner, Steven J., McKnight, Barbara, Psaty, Bruce M., Reiner, Alex P., Sargurupremraj, Muralidharan, Taylor, Kent D., Fornage, Myriam, Hamsten, Anders, März, Winfried, Rosendaal, Frits R., Souto, Juan Carlos, Dehghan, Abbas, Johnson, Andrew D., Morrison, Alanna C., O’Donnell, Christopher J., Smith, Nicholas L.
Published in Blood (28.02.2019)
Published in Blood (28.02.2019)
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