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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

Mercader, Josep M ; Udler, Miriam S ; Wessel, Jennifer ; Teslovich, Tanya M ; Caulkins, Lizz ; Barajas-Olmos, Francisco ; Boerwinkle, Eric ; Chen, Ling ; Contreras-Cubas, Cecilia ; Córdova, Emilio ; Correa, Adolfo ; DeFronzo, Ralph A ; Dolan, Lawrence ; Elliott, Amanda ; Floyd, James S ; Garay-Sevilla, Maria Eugenia ; García-Ortiz, Humberto ; Heard-Costa, Nancy L ; Jørgensen, Marit E ; Kang, Hyun Min ; Kelsey, Megan ; Linneberg, Allan ; Liu, Ching-Ti ; Liu, Jianjun ; Lyssenko, Valeriya ; Marcketta, Anthony ; Martínez-Hernández, Angélica ; Mayer-Davis, Elizabeth ; Morrison, Alanna C ; Ndungu, Anne ; Ng, Maggie C Y ; O'Dushlaine, Colm ; Post, Wendy S ; Vasan, Ramachandran S ; Rayner, N William ; Revilla-Monsalve, Cristina ; Santoro, Nicola ; Schurmann, Claudia ; Soberón, Xavier ; Strom, Tim M ; Thameem, Farook ; Torres, Jason M ; Vujkovic, Marijana ; Witte, Daniel R ; Atzmon, Gil ; Blangero, John ; Bonnycastle, Lori L ; Chan, Edmund ; Cheng, Ching-Yu ; Collins, Francis S ; de Vries, Paul S ; Glaser, Benjamin ; Gonzalez, Ma Elena ; Groop, Leif ; Kooner, Jaspal Singh ; Kwak, Soo Heon ; Laakso, Markku ; Nilsson, Peter ; Spector, Timothy D ; Tai, E Shyong ; Tuomilehto, Jaakko ; Wilson, James G ; Burke, Brian ; Carey, David J ; Frossard, Philippe ; Hwang, Mi Yeong ; Kim, Young Jin ; Kirchner, H Lester ; Lee, Jong-Young ; Lee, Juyoung ; Loos, Ruth J F ; Ma, Ronald C W ; Morris, Andrew D ; Palmer, Colin N A ; Pankow, James ; Rasheed, Asif ; Saleheen, Danish ; Sim, Xueling ; Small, Kerrin S ; Teo, Yik Ying ; Haiman, Christopher ; Hanis, Craig L ; Dewey, Frederick E ; Baras, Aris ; Gieger, Christian ; Meitinger, Thomas ; Lange, Leslie ; Pedersen, Oluf ; Zeitler, Philip ; Dabelea, Dana ; Abecasis, Goncalo ; Cox, Nancy J ; Sladek, Rob ; Meigs, James B ; Rotter, Jerome I ; Altshuler, David ; Burtt, Noël P ; Morris, Andrew P ; Florez, Jose C ; Boehnke, Michael

Nature (London), 2019-06, Vol.570 (7759), p.71-76 [Periódico revisado por pares]

England: Nature Publishing Group

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2
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications
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Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

Sterenborg, Rosalie B T M ; Li, Yong ; Marouli, Eirini ; Babajide, Oladapo ; Andreasen, Laura ; Astrup, Arne ; Åsvold, Bjørn Olav ; Bandinelli, Stefania ; Beekman, Marian ; Boutin, Thibaud ; Brown, Suzanne J ; Brumpton, Ben ; Campbell, Purdey J ; Cappola, Anne R ; Ceresini, Graziano ; Chaker, Layal ; Chasman, Daniel I ; Concas, Maria Pina ; Cross, Simone M ; Cucca, Francesco ; Deary, Ian J ; Kjaergaard, Alisa Devedzic ; Ellervik, Christina ; Eriksson, Johan G ; Freudenberg, Jan ; Fuchsberger, Christian ; Gieger, Christian ; Giulianini, Franco ; Graham, Sarah E ; Grarup, Niels ; Hansen, Torben ; Harding, Barbara N ; Haunsø, Stig ; Hayward, Caroline ; Hui, Jennie ; Ittermann, Till ; Jukema, J Wouter ; Kajantie, Eero ; Kanters, Jørgen K ; Kårhus, Line L ; Kiemeney, Lambertus A L M ; Kloppenburg, Margreet ; Kühnel, Brigitte ; Lahti, Jari ; Langenberg, Claudia ; Leese, Graham ; Li, Shuo ; Lominchar, Jesus V T ; Luan, Jian'an ; Martin, Nicholas G ; Matana, Antonela ; Meima, Marcel E ; Meitinger, Thomas ; Mitchell, Braxton D ; Møllehave, Line T ; Nauck, Matthias ; Netea-Maier, Romana T ; Noordam, Raymond ; Okada, Yukinori ; Palmer, Colin N A ; Peters, Annette ; Pietzner, Maik ; Psaty, Bruce M ; Punda, Ante ; Ray, Debashree ; Redmond, Paul ; Richards, J Brent ; Ryan, Kathleen A ; Olesen, Morten Salling ; Schultheiss, Ulla T ; Selvin, Elizabeth ; Siddiqui, Moneeza K ; Slagboom, P Eline ; Soto-Pedre, Enrique ; Spector, Tim D ; Spedicati, Beatrice ; Srinivasan, Sundararajan ; Starr, John M ; Stott, David J ; Torlak, Vesela ; Trompet, Stella ; Tuhkanen, Johanna ; Uitterlinden, André G ; van Heemst, Diana ; Vojinovic, Dina ; Waldenberger, Melanie ; Walsh, John P ; Willer, Cristen J ; Wilson, Scott G ; Wolffenbuttel, Bruce H R ; Wouters, Hanneke J C M ; Wright, Margaret J ; Yang, Qiong ; Zhu, Gu ; Zöllner, Sebastian ; Smit, Johannes W A ; Peeters, Robin P ; Köttgen, Anna ; Teumer, Alexander ; Medici, Marco

Nature communications, 2024-01, Vol.15 (1), p.888-888, Article 888 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
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Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility

Patsopoulos, Nikolaos A. ; Baranzini, Sergio E. ; Santaniello, Adam ; Shoostari, Parisa ; Cotsapas, Chris ; Vlachos, Ioannis S. ; Pers, Tune H. ; Brandes, Aaron ; White, Charles ; Panteliadis, Ioannis-Pavlos ; Robbins, Allison ; Andlauer, Till F. M. ; Zarzycki, Onigiusz ; Dubois, Bénédicte ; Søndergaard, Helle Bach ; Sellebjerg, Finn ; Ullum, Henrik ; Saarela, Janna ; Cournu-Rebeix, Isabelle ; Damotte, Vincent ; Fontaine, Bertrand ; Guillot-Noel, Lena ; Lathrop, Mark ; Vukusic, Sandra ; Berthele, Achim ; Pongratz, Viola ; Buck, Dorothea ; Knier, Benjamin ; Lill, Christina M. ; Zipp, Frauke ; Amoroso, Antonio ; Barizzone, Nadia ; Cavalla, Paola ; Comi, Giancarlo ; Cusi, Daniele ; Esposito, Federica ; Ferrè, Laura ; Galimberti, Daniela ; Guaschino, Clara ; Martinelli, Vittorio ; Moiola, Lucia ; Salvetti, Marco ; Vecchio, Domizia ; Zauli, Andrea ; Santoro, Silvia ; Zuccalà, Miriam ; Mescheriakova, Julia ; van Duijn, Cornelia ; Celius, Elisabeth G. ; Spurkland, Anne ; Comabella, Manuel ; Montalban, Xavier ; Alfredsson, Lars ; Hillert, Jan ; Jagodic, Maja ; Lindén, Magdalena ; Piehl, Fredrik ; Martin, Roland ; Sospedra, Mirela ; Baker, Amie ; Ban, Maria ; Hawkins, Clive ; Kalra, Seema ; Khadake, Jyoti ; Molyneux, Paul ; Neville, Matthew ; Thorpe, John ; Bradshaw, Elizabeth ; Caillier, Stacy J. ; Cree, Bruce A. C. ; Davis, Mary ; de Bakker, Paul W. I. ; Delgado, Silvia ; Dembele, Marieme ; Edwards, Keith ; Gourraud, Pierre-Antoine ; Haines, Jonathan L ; Kimbrough, Dorlan ; Isobe, Noriko ; Lathi, Ellen ; Lee, Michelle H. ; An, David ; Zimmer, Andrew ; Manrique, Clara P. ; Mitrovic, Mitja ; Piccio, Laura ; Weiner, Howard ; Compston, Alastair ; Harbo, Hanne F. ; Hauser, Stephen L. ; Stewart, Graeme ; Hadjigeorgiou, Georgios ; Taylor, Bruce ; Booth, David ; Kockum, Ingrid ; Oksenberg, Jorge R. ; Sawcer, Stephen ; Ivinson, Adrian J. ; Olsson, Tomas ; De Jager, Philip L.

Science (American Association for the Advancement of Science), 2019-09, Vol.365 (6460), p.1417 [Periódico revisado por pares]

United States: The American Association for the Advancement of Science

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4
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
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Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

Hottenga, Jouke- Jan ; Grallert, Harald ; Perry, John R B ; Rybin, Denis ; Min, Josine L ; Ulrich, Anna ; Zudina, Liudmila ; Gådin, Jesper R ; Jiang, Longda ; Fadista, Joao ; Stathopoulou, Maria G ; Willems, Sara M ; Tanaka, Toshiko ; O'Connell, Jeff R ; Saxena, Richa ; Pourcain, Beate St ; Timpson, Nicholas J ; Shin, So-Youn ; Amin, Najaf ; Smith, Albert V ; Verweij, Niek ; Goel, Anuj ; Johnson, Paul C D ; Johnson, Toby ; Kapur, Karen ; Thorleifsson, Gudmar ; Rasmussen-Torvik, Laura J ; Esko, Tõnu ; Mihailov, Evelin ; Fall, Tove ; Mahajan, Anubha ; Meyer, Julia ; Sarin, Antti-Pekka ; Shungin, Dmitry ; Luan, Jian'an ; Horikoshi, Momoko ; Sanna, Serena ; Zemunik, Tatijana ; Kovacs, Peter ; Hastie, Nicholas D ; Kuusisto, Johanna ; Laakso, Markku ; Hicks, Andrew A ; Rauramaa, Rainer ; Bandinelli, Stefania ; Thorand, Barbara ; Miljkovic, Iva ; Lind, Lars ; Doney, Alex ; Kivimaki, Mika ; Groves, Christopher J ; Herder, Christian ; Uusitupa, Matti ; Sattar, Naveed ; Pouta, Anneli ; Snieder, Harold ; Boerwinkle, Eric ; Magnusson, Patrik K ; Blüher, Matthias ; Wolffenbuttel, Bruce H R ; Province, Michael A ; Abecasis, Goncalo R ; Meigs, James B ; Hovingh, G Kees ; Lindström, Jaana ; Wilson, James F ; Bornstein, Stefan R ; Tönjes, Anke ; Winkelmann, Bernhard R ; Lakka, Timo A ; Keinanen-Kiukaanniemi, Sirkka M ; Saaristo, Timo E ; Tuomilehto, Jaakko ; Wareham, Nicholas J ; Hayward, Caroline ; Vitart, Veronique ; Altshuler, David ; Stumvoll, Michael ; Campbell, Harry ; van Duijn, Cornelia M ; Illig, Thomas ; Boehnke, Michael ; Shuldiner, Alan R ; Peyser, Patricia A ; Kardia, Sharon L R ; Navis, Gerjan ; Harst, Pim van der ; Smith, George Davey ; Soranzo, Nicole ; Boomsma, Dorret I ; Groop, Leif ; Hofman, Albert ; Munroe, Patricia B ; Watkins, Hugh ; Stefansson, Kari ; Karpe, Fredrik ; Lindgren, Cecilia M ; Ingelsson, Erik ; Morris, Andrew P ; Prokopenko, Inga

Nature communications, 2021, Vol.12 (1), p.24-18, Article 24 [Periódico revisado por pares]

England: Nature Publishing Group

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5
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
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Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

Dornbos, Peter ; Chaffin, Mark D. ; Liu, Dajiang J. ; Wang, Minxian ; Park, Joseph ; Aguilar-Salinas, Carlos A. ; Arnett, Donna K. ; Barajas-Olmos, Francisco ; Barzilai, Nir ; Bielak, Lawrence F. ; Bis, Joshua C. ; Blangero, John ; Boerwinkle, Eric ; Bottinger, Erwin ; Brody, Jennifer A. ; Broome, Jai G. ; Burtt, Noël P. ; Cade, Brian E. ; Chang, Yi-Cheng ; Chen, Yii-Der I. ; Choi, Won Jung ; Contreras-Cubas, Cecilia ; Curran, Joanne E. ; de Vries, Paul S. ; DeFronzo, Ralph A. ; Doddapaneni, Harsha ; Duggirala, Ravindranath ; Dutcher, Susan K. ; Emery, Leslie S. ; Freedman, Barry I. ; García-Ortiz, Humberto ; Gibbs, Richard A. ; Glaser, Benjamin ; Gonzalez, Clicerio ; Gonzalez-Villalpando, Maria Elena ; Graff, Mariaelisa ; Grarup, Niels ; Gupta, Namrata ; Hansen, Torben ; Hung, Yi-Jen ; Hwang, Mi Yeong ; Irvin, Marguerite R. ; Kang, Hyun Min ; Kardia, Sharon L.R. ; Kelly, Tanika ; Khan, Alyna T. ; Kim, Bong-Jo ; Kim, Young Jin ; Lange, Leslie A. ; Lee, Juyoung ; Lee, Seonwook ; Lehman, Donna M. ; Linneberg, Allan ; Liu, Jianjun ; Lyssenko, Valeriya ; Ma, Ronald C.W. ; Martínez-Hernández, Angélica ; Mathias, Rasika A. ; Meigs, James B. ; Meitinger, Thomas ; Metcalf, Ginger A. ; Mi, Xuenan ; Mohlke, Karen L. ; Montasser, May E. ; Moon, Jee-Young ; Morrison, Alanna C. ; Muzny, Donna M. ; Nelson, Sarah C. ; Nilsson, Peter M. ; O’Connell, Jeffrey R. ; Palmer, Nicholette D. ; Park, Cheol Joo ; Peralta, Juan M. ; Peyser, Patricia A. ; Preuss, Michael ; Qi, Qibin ; Rao, D.C. ; Reiner, Alexander P. ; Rich, Stephen S. ; Samani, Nilesh ; Schurmann, Claudia ; Seo, Daekwan ; Seo, Jeong-Sun ; Sim, Xueling ; Sladek, Rob ; So, Wing Yee ; Stilp, Adrienne M. ; Taylor, Kent D. ; Teo, Yik Ying ; Tsai, Michael Y. ; Vasan, Ramachandran S. ; Watkins, Hugh ; Weeks, Daniel E. ; Wilson, James G. ; Yanek, Lisa R. ; Rader, Daniel J. ; Rotter, Jerome I. ; McCarthy, Mark I. ; Flannick, Jason A. ; Khera, Amit V.

American journal of human genetics, 2022-01, Vol.109 (1), p.81-96 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study
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Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study

Wang, Yuxuan ; Selvaraj, Margaret Sunitha ; Li, Xihao ; Li, Zilin ; Holdcraft, Jacob A. ; Arnett, Donna K. ; Bis, Joshua C. ; Blangero, John ; Boerwinkle, Eric ; Bowden, Donald W. ; Cade, Brian E. ; Carlson, Jenna C. ; Carson, April P. ; Chen, Yii-Der Ida ; Curran, Joanne E. ; de Vries, Paul S. ; Dutcher, Susan K. ; Ellinor, Patrick T. ; Floyd, James S. ; Fornage, Myriam ; Freedman, Barry I. ; Gabriel, Stacey ; Germer, Soren ; Gibbs, Richard A. ; Guo, Xiuqing ; He, Jiang ; Heard-Costa, Nancy ; Hildalgo, Bertha ; Hou, Lifang ; Irvin, Marguerite R. ; Joehanes, Roby ; Kaplan, Robert C. ; Kardia, Sharon LR ; Kelly, Tanika N. ; Kim, Ryan ; Kooperberg, Charles ; Kral, Brian G. ; Levy, Daniel ; Li, Changwei ; Liu, Chunyu ; Lloyd-Jone, Don ; Loos, Ruth JF ; Mahaney, Michael C. ; Martin, Lisa W. ; Mathias, Rasika A. ; Minster, Ryan L. ; Mitchell, Braxton D. ; Montasser, May E. ; Morrison, Alanna C. ; Murabito, Joanne M. ; Naseri, Take ; O'Connell, Jeffrey R. ; Palmer, Nicholette D. ; Preuss, Michael H. ; Psaty, Bruce M. ; Raffield, Laura M. ; Rao, Dabeeru C. ; Redline, Susan ; Reiner, Alexander P. ; Rich, Stephen S. ; Ruepena, Muagututi’a Sefuiva ; Sheu, Wayne H.-H. ; Smith, Jennifer A. ; Smith, Albert ; Tiwari, Hemant K. ; Tsai, Michael Y. ; Viaud-Martinez, Karine A. ; Wang, Zhe ; Yanek, Lisa R. ; Zhao, Wei ; Rotter, Jerome I. ; Lin, Xihong ; Natarajan, Pradeep ; Peloso, Gina M.

American journal of human genetics, 2023-10, Vol.110 (10), p.1704-1717 [Periódico revisado por pares]

United States: Elsevier Inc

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7
Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level
Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level
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Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level

Liang, Jingjing ; Cade, Brian E. ; He, Karen Y. ; Wang, Heming ; Lee, Jiwon ; Sofer, Tamar ; Williams, Stephanie ; Li, Ruitong ; Chen, Han ; Gottlieb, Daniel J. ; Evans, Daniel S. ; Guo, Xiuqing ; Gharib, Sina A. ; Hale, Lauren ; Hillman, David R. ; Lutsey, Pamela L. ; Mukherjee, Sutapa ; Ochs-Balcom, Heather M. ; Palmer, Lyle J. ; Rhodes, Jessica ; Purcell, Shaun ; Patel, Sanjay R. ; Saxena, Richa ; Stone, Katie L. ; Tang, Weihong ; Tranah, Gregory J. ; Boerwinkle, Eric ; Lin, Xihong ; Liu, Yongmei ; Psaty, Bruce M. ; Vasan, Ramachandran S. ; Cho, Michael H. ; Manichaikul, Ani ; Silverman, Edwin K. ; Barr, R. Graham ; Rich, Stephen S. ; Rotter, Jerome I. ; Wilson, James G. ; Redline, Susan ; Zhu, Xiaofeng

American journal of human genetics, 2019-11, Vol.105 (5), p.1057-1068 [Periódico revisado por pares]

United States: Elsevier Inc

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8
Genome‐wide association study for time to failure of kidney transplants from African American deceased donors
Genome‐wide association study for time to failure of kidney transplants from African American deceased donors
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Genome‐wide association study for time to failure of kidney transplants from African American deceased donors

Divers, Jasmin ; Ma, Lijun ; Brown, William Mark ; Palmer, Nicholette D. ; Choi, Young ; Israni, Ajay K. ; Pastan, Stephen O. ; Julian, Bruce A. ; Gaston, Robert S. ; Hicks, Pamela J. ; Reeves‐Daniel, Amber M. ; Freedman, Barry I.

Clinical transplantation, 2020-06, Vol.34 (6), p.e13827-n/a [Periódico revisado por pares]

Denmark

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9
Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure
Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure
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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

Wang, Heming ; Noordam, Raymond ; Cade, Brian E ; Schwander, Karen ; Winkler, Thomas W ; Lee, Jiwon ; Sung, Yun Ju ; Bentley, Amy R ; Manning, Alisa K ; Kilpeläinen, Tuomas O ; Ilkov, Marjan ; Brown, Michael R ; Horimoto, Andrea R ; Richard, Melissa ; Bartz, Traci M ; Vojinovic, Dina ; Lim, Elise ; Nierenberg, Jovia L ; Chitrala, Kumaraswamynaidu ; Rankinen, Tuomo ; Musani, Solomon K ; Franceschini, Nora ; Rauramaa, Rainer ; Zee, Phyllis C ; Harris, Sarah E ; van der Most, Peter J ; Munroe, Patricia B ; Palmer, Nicholette D ; Kühnel, Brigitte ; Weiss, Stefan ; Wen, Wanqing ; Lyytikäinen, Leo-Pekka ; O'Connell, Jeff ; Eiriksdottir, Gudny ; Launer, Lenore J ; de Vries, Paul S ; Arking, Dan E ; Chen, Han ; Boerwinkle, Eric ; Krieger, Jose E ; Schreiner, Pamela J ; Sidney, Stephen ; Rice, Kenneth ; Chen, Yii-Der Ida ; Luik, Annemarie I ; Ikram, M Arfan ; Uitterlinden, André G ; Amin, Najaf ; Xu, Hanfei ; Levy, Daniel ; He, Jiang ; Lohman, Kurt K ; Rice, Treva K ; Sims, Mario ; Sofer, Tamar ; Rich, Stephen S ; Palmas, Walter ; Yao, Jie ; Guo, Xiuqing ; Rotter, Jerome I ; Biermasz, Nienke R ; Mook-Kanamori, Dennis O ; Martin, Lisa W ; Gottlieb, Daniel J ; Heikkinen, Sami ; Mägi, Reedik ; Metspalu, Andres ; Starr, John M ; Waken, R J ; Gao, Chuan ; Peters, Annette ; Strauch, Konstantin ; Meitinger, Thomas ; Völker, Uwe ; Dörr, Marcus ; Shu, Xiao-Ou ; Mukherjee, Sutapa ; Hillman, David R ; Kähönen, Mika ; Wagenknecht, Lynne E ; Palmer, Lyle J ; Lehtimäki, Terho ; Morrison, Alanna C ; Pereira, Alexandre C ; Fornage, Myriam ; Psaty, Bruce M ; van Duijn, Cornelia M ; Bouchard, Claude ; Fox, Ervin R ; Kooperberg, Charles ; Zhu, Xiaofeng ; Lakka, Timo A ; Esko, Tõnu ; North, Kari E ; Deary, Ian J ; Snieder, Harold ; Penninx, Brenda W J H ; Gauderman, W James ; Rao, Dabeeru C ; van Heemst, Diana

Molecular psychiatry, 2021-11, Vol.26 (11), p.6293-6304 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Insight into the genetic architecture of back pain and its risk factors from a study of 509,000 individuals
Insight into the genetic architecture of back pain and its risk factors from a study of 509,000 individuals
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Insight into the genetic architecture of back pain and its risk factors from a study of 509,000 individuals

Freidin, Maxim B ; Tsepilov, Yakov A ; Palmer, Melody ; Karssen, Lennart C ; Suri, Pradeep ; Aulchenko, Yurii S ; Williams, Frances M K

Pain (Amsterdam), 2019-06, Vol.160 (6), p.1361-1373 [Periódico revisado por pares]

United States

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