Zobrazeno 1 - 10
of 142
pro vyhledávání: '"Duggan, David J."'
Autor:
Jaworek, Thomas, Xu, Huichun, Attia, John, Veldink, Jan H, Walters, Robin G, Weir, David R, Woo, Daniel, Worrall, Bradford B, Hong, Charles C, Ross, Owen, Zand, Ramin, Leeuw, Frank-Erik de, Lindgren, Arne G, Bell, Steven, Pare, Guillaume, Anderson, Christopher D, Markus, Hugh S, Jern, Christina, Malik, Rainer, Dichgans, Martin, Mitchell, Braxton D, Kittner, Steven J, Consortium, Early Onset Stroke Genetics Consortium of the International Stroke Genetics, Benavente, Oscar R, Boncoraglio, Giorgio B, Butterworth, Adam, Dissections, Cervical Artery, Patients, Ischemic Stroke, Carcel-Marquez, Jara, Chen, Zhengming, Chong, Michael, Gaynor, Brady J, Cruchaga, Carlos, Cushman, Mary, Danesh, John, Debette, Stephanie, Duggan, David J, Durda, Jon Peter, Engstrom, Gunnar, Enzinger, Chris, Faul, Jessica D, Fecteau, Natalie S, Cole, John W, Fernandez-Cadenas, Israel, Gieger, Christian, Giese, Anne-Katrin, Grewal, Raji P, Grittner, Ulrike, Havulinna, Aki S, Heitsch, Laura, Hochberg, Marc C, Holliday, Elizabeth, Hu, Jie, Rannikmae, Kristiina, Ilinca, Andreea, Consortium, INVENT, Irvin, Marguerite R, Jackson, Rebecca D, Jacob, Mina A, Janssen, Raquel Rabionet, Jimenez-Conde, Jordi, Johnson, Julie A, Kamatani, Yoichiro, Kardia, Sharon L, Stanne, Tara M, Koido, Masaru, Kubo, Michiaki, Lange, Leslie, Lee, Jin-Moo, Lemmens, Robin, Levi, Christopher R, Li, Jiang, Li, Liming, Lin, Kuang, Lopez, Haley, Tomppo, Liisa, Luke, Sothear, Maguire, Jane, McArdle, Patrick F, McDonough, Caitrin W, Meschia, James F, Metso, Tiina, Muller-Nurasyid, Martina, O'Connor, Timothy D, O'Donnell, Martin, Peddareddygari, Leema R, Abedi, Vida, Pera, Joanna, Perry, James A, Peters, Annette, Putaala, Jukka, Ray, Debashree, Rexrode, Kathryn, Ribases, Marta, Rosand, Jonathan, Rothwell, Peter M, Rundek, Tatjana, Amouyel, Philippe, Ryan, Kathleen A, Sacco, Ralph L, Salomaa, Veikko, Sanchez-Mora, Cristina, Schmidt, Reinhold, Sharma, Pankaj, Slowik, Agnieszka, Smith, Jennifer A, Smith, Nicholas L, Wassertheil-Smoller, Sylvia, Armstrong, Nicole D, Soederholm, Martin, Stine, O. C., Strbian, Daniel, Sudlow, Cathie L, Tatlisumak, Turgut, Terao, Chikashi, Thijs, Vincent, Torres-Aguila, Nuria P, Tregouet, David-Alexandre, Tuladhar, Anil M
Publikováno v:
Neurology 99(16), e1738-e1754 (2022). doi:10.1212/WNL.0000000000201006
Jaworek, T, Xu, H, Gaynor, B, Cole, J, Rannikmae, K, Stanne, T M, Tomppo, L, Abedi, V, Amouyel, P, Armstrong, N, Attia, J, Bell, S, Benavente, O R, Boncoraglio, G B, Butterworth, A S, Carcel-Marquez, J, Chen, Z, Chong, M, Cruchaga, C, Cushman, M, Danesh, J, Debette, S, Duggan, D, Durda, J P, Engstrom, G, Enzinger, C, Faul, J D, Fecteau, N, Fernandez-Cadenas, I, Gieger, C, Giese, A-K, Grewal, R P, Grittner, U, Havulinna, A S, Heitsch, L, Hochberg, M, Holliday, E G, Zhu, J, Llinca, A, Irvin, M R, Jackson, R D, Jacob, M, Rabionet-Janssen, R, Jimenez-Conde, J, Johnson, J A, Kamatani, Y, Kardia, S L R, Koido, M, Kubo, M, Lange, L A, Lee, J-M, Lemmens, R, Levi, C, Li, J, Lin, K, Lopez, H, Maguire, J M, Luke, S, McArdle, P F, McDonough, C W, Meschia, J, Metso, T M, Müller-Nurasyid, M, O'Connor, T, Peddareddygari, L R, O'Donnell, M, Pera, J, Perry, J, Peters, A, Putaala, J, Ray, D, Rexrode, K M, Ribases, M, Rosand, J, Rothwell, P M, Rundek, T, Ryan, K, Sacco, R L, Salomaa, V, Sánchez-Mora, C, Schmidt, R, Sharma, P, Slowik, A, Smith, J, Smith, N L, Wassertheil-Smoller, S, Söderholm, M, Stine, C, Strbian, D, Sudlow, C L M, Tatlisumak, T, Terao, C, Thijs, V, Torres-Aguila, N, Tregouet, D-A, Tuladhar, A M, Veldink, J H, Walters, R G, Weir, D R, Woo, D, Worrall, B B, Hong, C, Ross, O A, Zand, R, de Leeuw, F-E, Lindgren, A, Pare, G, Anderson, C D, Markus, H S, Jern, C, Malik, R, Dichgans, M, Mitchell, B D & Kittner, S J 2022, ' Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke ', Neurology, vol. 99, no. 16, pp. e1738-e1754 . https://doi.org/10.1212/WNL.0000000000201006
Jaworek, T, Xu, H, Gaynor, B, Cole, J, Rannikmae, K, Stanne, T M, Tomppo, L, Abedi, V, Amouyel, P, Armstrong, N, Attia, J, Bell, S, Benavente, O R, Boncoraglio, G B, Butterworth, A S, Carcel-Marquez, J, Chen, Z, Chong, M, Cruchaga, C, Cushman, M, Danesh, J, Debette, S, Duggan, D, Durda, J P, Engstrom, G, Enzinger, C, Faul, J D, Fecteau, N, Fernandez-Cadenas, I, Gieger, C, Giese, A-K, Grewal, R P, Grittner, U, Havulinna, A S, Heitsch, L, Hochberg, M, Holliday, E G, Zhu, J, Llinca, A, Irvin, M R, Jackson, R D, Jacob, M, Rabionet-Janssen, R, Jimenez-Conde, J, Johnson, J A, Kamatani, Y, Kardia, S L R, Koido, M, Kubo, M, Lange, L A, Lee, J-M, Lemmens, R, Levi, C, Li, J, Lin, K, Lopez, H, Maguire, J M, Luke, S, McArdle, P F, McDonough, C W, Meschia, J, Metso, T M, Müller-Nurasyid, M, O'Connor, T, Peddareddygari, L R, O'Donnell, M, Pera, J, Perry, J, Peters, A, Putaala, J, Ray, D, Rexrode, K M, Ribases, M, Rosand, J, Rothwell, P M, Rundek, T, Ryan, K, Sacco, R L, Salomaa, V, Sánchez-Mora, C, Schmidt, R, Sharma, P, Slowik, A, Smith, J, Smith, N L, Wassertheil-Smoller, S, Söderholm, M, Stine, C, Strbian, D, Sudlow, C L M, Tatlisumak, T, Terao, C, Thijs, V, Torres-Aguila, N, Tregouet, D-A, Tuladhar, A M, Veldink, J H, Walters, R G, Weir, D R, Woo, D, Worrall, B B, Hong, C, Ross, O A, Zand, R, de Leeuw, F-E, Lindgren, A, Pare, G, Anderson, C D, Markus, H S, Jern, C, Malik, R, Dichgans, M, Mitchell, B D & Kittner, S J 2022, ' Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke ', Neurology, vol. 99, no. 16, pp. e1738-e1754 . https://doi.org/10.1212/WNL.0000000000201006
Background and Objectives:Current genome-wide association studies of ischemic stroke have focused primarily on late onset disease. As a complement to these studies, we sought to identifythe contribution of common genetic variants to risk of early ons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f90257f92b8480b7d7d014740c0376c
https://lirias.kuleuven.be/handle/20.500.12942/716243
https://lirias.kuleuven.be/handle/20.500.12942/716243
Autor:
The WECARE Study Collaborative Group, Brooks, Jennifer D., Teraoka, Sharon N., Bernstein, Leslie, Mellemkjær, Lene, Malone, Kathleen E., Lynch, Charles F., Haile, Robert W., Concannon, Patrick, Reiner, Anne S., Duggan, David J., Schiermeyer, Katherine, Bernstein, Jonine L., Figueiredo, Jane C.
Publikováno v:
Cancer Causes & Control, 2013 Aug 01. 24(8), 1605-1614.
Externí odkaz:
https://www.jstor.org/stable/24717700
Autor:
Poole, Elizabeth M., Curtin, Karen, Hsu, Li, Duggan, David J., Makar, Karen W., Xiao, Liren, Carlson, Christopher S., Caan, Bette J., Potter, John D., Slattery, Martha L., Ulrich, Cornelia M.
Publikováno v:
In Cancer Epidemiology April 2012 36(2):e104-e110
Akademický článek
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Autor:
Cheng, Ting-Yuan David, Ilozumba, Mmadili N, Balavarca, Yesilda, Neuhouser, Marian L, Miller, Joshua W, Beresford, Shirley A A, Zheng, Yingye, Song, Xiaoling, Duggan, David J, Toriola, Adetunji T, Bailey, Lynn B, Green, Ralph, Caudill, Marie A, Ulrich, Cornelia M
Publikováno v:
Journal of Nutrition; Apr2022, Vol. 152 Issue 4, p1099-1106, 8p
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Brisbin Abra G, Asmann Yan W, Song Honglin, Tsai Ya-Yu, Aakre Jeremiah A, Yang Ping, Jenkins Robert B, Pharoah Paul, Schumacher Fredrick, Conti David V, Duggan David J, Jenkins Mark, Hopper John, Gallinger Steven, Newcomb Polly, Casey Graham, Sellers Thomas A, Fridley Brooke L
Publikováno v:
BMC Medical Genetics, Vol 12, Iss 1, p 156 (2011)
Abstract Background Human chromosomal region 8q24 contains several genes which could be functionally related to cancer, including the proto-oncogene c-MYC. However, the abundance of associations around 128 Mb on chromosome 8 could mask the appearance
Externí odkaz:
https://doaj.org/article/c97ed3eafbbc47f893309e0e5ca64762
Autor:
Wallace Robert, Hammad Nazik, Marshall James R, Sarto Gloria E, Rajkovic Aleksandar, Beresford Shirley AA, Hsu Li, Curtin Karen, Muehling Jill, Duggan David J, Slattery Martha L, Hutter Carolyn M, Makar Karen W, Prentice Ross L, Caan Bette J, Potter John D, Peters Ulrike
Publikováno v:
BMC Cancer, Vol 10, Iss 1, p 670 (2010)
Abstract Background Genome-wide association studies and subsequent replication studies have shown that single nucleotide polymorphisms (SNPs) in the chromosomal region 8q24 are associated with colorectal cancer susceptibility. Methods We examined 11
Externí odkaz:
https://doaj.org/article/290b09c4c3b34dcea1bb091bceec5f0f
Autor:
Yau, Michelle S, Yerges-Armstrong, Laura M, Liu, Youfang, Lewis, Cora E, Duggan, David J, Renner, Jordan B, Torner, James, Felson, David T, McCulloch, Charles E, Kwoh, C Kent, Nevitt, Michael C, Hochberg, Marc C, Mitchell, Braxton D, Jordan, Joanne M, Jackson, Rebecca D
Publikováno v:
Arthritis & rheumatology (Hoboken, N.J.), vol 69, iss 2
ObjectiveA major barrier to genetic studies of osteoarthritis (OA) is the need to obtain large numbers of individuals with standardized radiographic evaluations for OA. To address this gap, we performed a genome-wide association study (GWAS) of radio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::e040778b3619e6dd65ca554e101646f9
https://escholarship.org/uc/item/4tx9m7zb
https://escholarship.org/uc/item/4tx9m7zb
Autor:
Reppe, Sjur, Wang, Yunpeng, Thompson, Wesley K., McEvoy, Linda K., Schork, Andrew J., Zuber, Verena, LeBlanc, Marissa, Bettella, Francesco, Mills, Ian G., Desikan, Rahul S., Djurovic, Srdjan, Gautvik, Kaare M., Dale, Anders M., Andreassen, Ole A., Estrada, Karol, Styrkarsdottir, Unnur, Evangelou, Evangelos, Hsu, Yi Hsiang, Duncan, Emma L., Ntzani, Evangelia E., Oei, Ling, Albagha, Omar M.E., Amin, Najaf, Kemp, John P., Koller, Daniel L., Li, Guo, Liu, Ching Ti, Minster, Ryan L., Moayyeri, Alireza, Vandenput, Liesbeth, Willner, Dana, Xiao, Su Mei, Yerges-Armstrong, Laura M., Zheng, Hou Feng, Alonso, Nerea, Eriksson, Joel, Kammerer, Candace M., Kaptoge, Stephen K., Leo, Paul J., Thorleifsson, Gudmar, Wilson, Scott G., Wilson, James F., Aalto, Ville, Alen, Markku, Aragaki, Aaron K., Aspelund, Thor, Center, Jacqueline R., Dailiana, Zoe, Duggan, David J., Garcia, Melissa, Garcia-Giralt, Natàlia, Giroux, Sylvie, Hallmans, Göran, Hocking, Lynne J., Husted, Lise Bjerre, Jameson, Karen A., Khusainova, Rita, Kim, Ghi Su, Kooperberg, Charles, Koromila, Theodora, Kruk, Marcin, Laaksonen, Marika, Lacroix, Andrea Z., Lee, Seung Hun, Leung, Ping C., Lewis, Joshua R., Masi, Laura, Mencej-Bedrac, Simona, Nguyen, Tuan V., Nogues, Xavier, Patel, Millan S., Prezelj, Janez, Rose, Lynda M., Scollen, Serena, Siggeirsdottir, Kristin, Smith, Albert V., Svensson, Olle, Trompet, Stella, Trummer, Olivia, Van Schoor, Natasja M., Woo, Jean, Zhu, Kun, Balcells, Susana, Brandi, Maria Luisa, Buckley, Brendan M., Cheng, Sulin, Christiansen, Claus, Cooper, Cyrus, Dedoussis, George, Ford, Ian, Frost, Morten, Goltzman, David, González-Macías, Jesús, Kähönen, Mika, Karlsson, Magnus, Khusnutdinova, Elza, Koh, Jung Min, Kollia, Panagoula, Langdahl, Bente Lomholt, Leslie, William D., Lips, Paul, Ljunggren, Östen, Lorenc, Roman S., Marc, Janja, Mellström, Dan, Obermayer-Pietsch, Barbara, Olmos, José M., Pettersson-Kymmer, Ulrika, Reid, David M., Riancho, José A., Ridker, Paul M., Rousseau, François, Slagboom, P. Eline, Tang, Nelson L.S., Urreizti, Roser, Van Hul, Wim, Viikari, Jorma, Zarrabeitia, María T., Aulchenko, Yurii S., Castano-Betancourt, Martha, Grundberg, Elin, Herrera, Lizbeth, Ingvarsson, Thorvaldur, Johannsdottir, Hrefna, Kwan, Tony, Li, Rui, Luben, Robert, Medina-Gómez, Carolina, Palsson, Stefan Th, Rotter, Jerome I., Sigurdsson, Gunnar, Van Meurs, Joyce B.J., Verlaan, Dominique, Williams, Frances M.K., Wood, Andrew R., Zhou, Yanhua, Pastinen, Tomi, Raychaudhuri, Soumya, Cauley, Jane A., Chasman, Daniel I., Clark, Graeme R., Cummings, Steven R., Danoy, Patrick, Dennison, Elaine M., Eastell, Richard, Eisman, John A., Gudnason, Vilmundur, Hofman, Albert, Jackson, Rebecca D., Jones, Graeme, Jukema, J. Wouter, Khaw, Kay Tee, Lehtimäki, Terho, Liu, Yongmei, Lorentzon, Mattias, McCloskey, Eugene, Mitchell, Braxton D., Nandakumar, Kannabiran, Nicholson, Geoffrey C., Oostra, Ben A., Peacock, Munro, Pols, Huibert A.P., Prince, Richard L., Raitakari, Olli, Reid, Ian R., Robbins, John, Sambrook, Philip N., Sham, Pak Chung, Shuldiner, Alan R., Tylavsky, Frances A., Van Duijn, Cornelia M., Wareham, Nick J., Cupples, L. Adrienne, Econs, Michael J., Evans, David M., Harris, Tamara B., Kung, Annie Wai Chee, Psaty, Bruce M., Reeve, Jonathan, Spector, Timothy D., Streeten, Elizabeth A., Zillikens, M. Carola, Thorsteinsdottir, Unnur, Ohlsson, Claes, Karasik, David, Richards, J. Brent, Brown, Matthew A., Stefansson, Kari, Uitterlinden, André G., Ralston, Stuart H., Ioannidis, John P.A., Kiel, Douglas P., Rivadeneira, Fernando
Publikováno v:
PLoS ONE, 10(12):e0144531. Public Library of Science
Reppe, S, Wang, Y, Thompson, W K, McEvoy, L K, Schork, A J, Zuber, V, LeBlanc, M, Bettella, F, Mills, I G, Desikan, R S, Djurovic, S, Gautvik, K M, Dale, A M, Andreassen, O A, Estrada, K, Styrkarsdottir, U, Evangelou, E, Hsu, Y H, Duncan, E L, Ntzani, E E, Oei, L, Albagha, O M E, Amin, N, Kemp, J P, Koller, D L, Li, G, Liu, C T, Minster, R L, Moayyeri, A, Vandenput, L, Willner, D, Xiao, S M, Yerges-Armstrong, L M, Zheng, H F, Alonso, N, Eriksson, J, Kammerer, C M, Kaptoge, S K, Leo, P J, Thorleifsson, G, Wilson, S G, Wilson, J F, Aalto, V, Alen, M, Aragaki, A K, Aspelund, T, Center, J R, Dailiana, Z, Duggan, D J, Garcia, M, Garcia-Giralt, N, Giroux, S, Hallmans, G, Hocking, L J, Husted, L B, Jameson, K A, Khusainova, R, Kim, G S, Kooperberg, C, Koromila, T, Kruk, M, Laaksonen, M, Lacroix, A Z, Lee, S H, Leung, P C, Lewis, J R, Masi, L, Mencej-Bedrac, S, Nguyen, T V, Nogues, X, Patel, M S, Prezelj, J, Rose, L M, Scollen, S, Siggeirsdottir, K, Smith, A V, Svensson, O, Trompet, S, Trummer, O, Van Schoor, N M, Woo, J, Zhu, K, Balcells, S, Brandi, M L, Buckley, B M, Cheng, S, Christiansen, C, Cooper, C, Dedoussis, G, Ford, I, Frost, M, Goltzman, D, González-Macías, J, Kähönen, M, Karlsson, M, Khusnutdinova, E, Koh, J M, Kollia, P, Langdahl, B L, Leslie, W D, Lips, P, Ljunggren, Ö, Lorenc, R S, Marc, J, Mellström, D, Obermayer-Pietsch, B, Olmos, J M, Pettersson-Kymmer, U, Reid, D M, Riancho, J A, Ridker, P M, Rousseau, F, Slagboom, P E, Tang, N L S, Urreizti, R, Van Hul, W, Viikari, J, Zarrabeitia, M T, Aulchenko, Y S, Castano-Betancourt, M, Grundberg, E, Herrera, L, Ingvarsson, T, Johannsdottir, H, Kwan, T, Li, R, Luben, R, Medina-Gómez, C, Palsson, S T, Rotter, J I, Sigurdsson, G, Van Meurs, J B J, Verlaan, D, Williams, F M K, Wood, A R, Zhou, Y, Pastinen, T, Raychaudhuri, S, Cauley, J A, Chasman, D I, Clark, G R, Cummings, S R, Danoy, P, Dennison, E M, Eastell, R, Eisman, J A, Gudnason, V, Hofman, A, Jackson, R D, Jones, G, Jukema, J W, Khaw, K T, Lehtimäki, T, Liu, Y, Lorentzon, M, McCloskey, E, Mitchell, B D, Nandakumar, K, Nicholson, G C, Oostra, B A, Peacock, M, Pols, H A P, Prince, R L, Raitakari, O, Reid, I R, Robbins, J, Sambrook, P N, Sham, P C, Shuldiner, A R, Tylavsky, F A, Van Duijn, C M, Wareham, N J, Cupples, L A, Econs, M J, Evans, D M, Harris, T B, Kung, A W C, Psaty, B M, Reeve, J, Spector, T D, Streeten, E A, Zillikens, M C, Thorsteinsdottir, U, Ohlsson, C, Karasik, D, Richards, J B, Brown, M A, Stefansson, K, Uitterlinden, A G, Ralston, S H, Ioannidis, J P A, Kiel, D P, Rivadeneira, F & GEFOS Consortium 2015, ' Genetic sharing with cardiovascular disease risk factors and diabetes reveals novel bone mineral density loci ', PLoS ONE, vol. 10, no. 12, e0144531 . https://doi.org/10.1371/journal.pone.0144531
Reppe, S, Wang, Y, Thompson, W K, McEvoy, L K, Schork, A J, Zuber, V, LeBlanc, M, Bettella, F, Mills, I G, Desikan, R S, Djurovic, S, Gautvik, K M, Dale, A M, Andreassen, O A, Estrada, K, Styrkarsdottir, U, Evangelou, E, Hsu, Y H, Duncan, E L, Ntzani, E E, Oei, L, Albagha, O M E, Amin, N, Kemp, J P, Koller, D L, Li, G, Liu, C T, Minster, R L, Moayyeri, A, Vandenput, L, Willner, D, Xiao, S M, Yerges-Armstrong, L M, Zheng, H F, Alonso, N, Eriksson, J, Kammerer, C M, Kaptoge, S K, Leo, P J, Thorleifsson, G, Wilson, S G, Wilson, J F, Aalto, V, Alen, M, Aragaki, A K, Aspelund, T, Center, J R, Dailiana, Z, Duggan, D J, Garcia, M, Garcia-Giralt, N, Giroux, S, Hallmans, G, Hocking, L J, Husted, L B, Jameson, K A, Khusainova, R, Kim, G S, Kooperberg, C, Koromila, T, Kruk, M, Laaksonen, M, Lacroix, A Z, Lee, S H, Leung, P C, Lewis, J R, Masi, L, Mencej-Bedrac, S, Nguyen, T V, Nogues, X, Patel, M S, Prezelj, J, Rose, L M, Scollen, S, Siggeirsdottir, K, Smith, A V, Svensson, O, Trompet, S, Trummer, O, Van Schoor, N M, Woo, J, Zhu, K, Balcells, S, Brandi, M L, Buckley, B M, Cheng, S, Christiansen, C, Cooper, C, Dedoussis, G, Ford, I, Frost, M, Goltzman, D, González-Macías, J, Kähönen, M, Karlsson, M, Khusnutdinova, E, Koh, J M, Kollia, P, Langdahl, B L, Leslie, W D, Lips, P, Ljunggren, Ö, Lorenc, R S, Marc, J, Mellström, D, Obermayer-Pietsch, B, Olmos, J M, Pettersson-Kymmer, U, Reid, D M, Riancho, J A, Ridker, P M, Rousseau, F, Slagboom, P E, Tang, N L S, Urreizti, R, Van Hul, W, Viikari, J, Zarrabeitia, M T, Aulchenko, Y S, Castano-Betancourt, M, Grundberg, E, Herrera, L, Ingvarsson, T, Johannsdottir, H, Kwan, T, Li, R, Luben, R, Medina-Gómez, C, Palsson, S T, Rotter, J I, Sigurdsson, G, Van Meurs, J B J, Verlaan, D, Williams, F M K, Wood, A R, Zhou, Y, Pastinen, T, Raychaudhuri, S, Cauley, J A, Chasman, D I, Clark, G R, Cummings, S R, Danoy, P, Dennison, E M, Eastell, R, Eisman, J A, Gudnason, V, Hofman, A, Jackson, R D, Jones, G, Jukema, J W, Khaw, K T, Lehtimäki, T, Liu, Y, Lorentzon, M, McCloskey, E, Mitchell, B D, Nandakumar, K, Nicholson, G C, Oostra, B A, Peacock, M, Pols, H A P, Prince, R L, Raitakari, O, Reid, I R, Robbins, J, Sambrook, P N, Sham, P C, Shuldiner, A R, Tylavsky, F A, Van Duijn, C M, Wareham, N J, Cupples, L A, Econs, M J, Evans, D M, Harris, T B, Kung, A W C, Psaty, B M, Reeve, J, Spector, T D, Streeten, E A, Zillikens, M C, Thorsteinsdottir, U, Ohlsson, C, Karasik, D, Richards, J B, Brown, M A, Stefansson, K, Uitterlinden, A G, Ralston, S H, Ioannidis, J P A, Kiel, D P, Rivadeneira, F & GEFOS Consortium 2015, ' Genetic sharing with cardiovascular disease risk factors and diabetes reveals novel bone mineral density loci ', PLoS ONE, vol. 10, no. 12, e0144531 . https://doi.org/10.1371/journal.pone.0144531
Bone Mineral Density (BMD) is a highly heritable trait, but genome-wide association studies have identified few genetic risk factors. Epidemiological studies suggest associations between BMD and several traits and diseases, but the nature of the sugg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::37bdc47e2e6f90e7184385ce996bf2f2
https://research.vumc.nl/en/publications/9a1c8f12-213e-4008-955d-a626984b32ba
https://research.vumc.nl/en/publications/9a1c8f12-213e-4008-955d-a626984b32ba