Rezultaty - Take Naseri

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  1. 1
    Comparing age and sex trends of chlamydia, gonorrhoea, hepatitis and syphilis infections in Samoa in 2012 and 2017

    Comparing age and sex trends of chlamydia, gonorrhoea, hepatitis and syphilis infections in Samoa in 2012 and 2017 od Carney, Robert, Howells, Michaela, Tanumafili, Aaone, Matalavea, Athena, Gafa, Judith, Leausa Toleafoa, Dr Take Naseri

    Wydane 2020
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  2. 2
    Trends in diabetes and obesity in Samoa over 35 years, 1978–2013

    Trends in diabetes and obesity in Samoa over 35 years, 1978–2013 od Sophia Lin, Take Naseri, Christine Linhart, Stephen Morrell, Richard Taylor, Stephen T. McGarvey, Dianna J. Magliano, Paul Zimmet

    Wydane 2016
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  3. 3
    Serum anti-mullerian hormone levels and age among Samoan women

    Serum anti-mullerian hormone levels and age among Samoan women od Grace O’Brien, Geralyn Lambert‐Messerlian, Nicola L. Hawley, Ulai T. Fidow, Take Naseri, Muagututi‘a Sefuiva Reupena, Erin E. Kershaw, M Azar, Martha M. Pangburn, Stephen T. McGarvey

    Wydane 2025
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  4. 4
    Psychosocial correlates of HbA1c among adult Samoans without diabetes

    Psychosocial correlates of HbA1c among adult Samoans without diabetes od Anna C. Rivara, Lacey W. Heinsberg, Jenna C. Carlson, Alysa Pomer, Take Naseri, Muagututia Seifuiva Reupena, Courtney C. Choy, Dongqing Wang, Erin E. Kershaw, Satupaitea Viali, Stephen T. McGarvey, Nicola L. Hawley

    Wydane 2025
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  5. 5
    A thrifty variant in CREBRF strongly influences body mass index in Samoans

    A thrifty variant in CREBRF strongly influences body mass index in Samoans od Ryan L. Minster, Nicola L. Hawley, Chi-Ting Su, Guangyun Sun, Erin E. Kershaw, Hong Cheng, Olive D. Buhule, Jerome Lin, Muagututi‘a Sefuiva Reupena, Satupaitea Viali, John Tuitele, Take Naseri, Zsolt Urbán, Ranjan Deka, Daniel E. Weeks, Stephen T. McGarvey

    Wydane 2016
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  6. 6
    Discordant association of the CREBRF rs373863828 A allele with increased BMI and protection from type 2 diabetes in Māori and Pacific (Polynesian) people living in Aotearoa/New Zealand

    Discordant association of the CREBRF rs373863828 A allele with increased BMI and protection from type 2 diabetes in Māori and Pacific (Polynesian) people living in Aotearoa/New Zea... od Mohanraj Krishnan, Tanya J. Major, Ruth Topless, Ofa Dewes, Lennex Hsueh‐Lin Yu, John M. D. Thompson, Lesley McCowan, Janak de Zoysa, Lisa K. Stamp, Nicola Dalbeth, Jennie Harré Hindmarsh, Nuku Rapana, Ranjan Deka, Winston W. H. Eng, Daniel E. Weeks, Ryan L. Minster, Stephen T. McGarvey, Satupaitea Viali, Take Naseri, Muagututi‘a Sefuiva Reupena, Phillip Wilcox, David R. Grattan, Peter R. Shepherd, Andrew N. Shelling, Rinki Murphy, Tony R. Merriman

    Wydane 2018
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  7. 7
    Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania

    Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania od Tom Parks, Mariana Mirabel, Joseph Kado, Kathryn Auckland, Jarosław Nowak, Anna Rautanen, Alexander J. Mentzer, Éloi Marijon, Xavier Jouven, Mai Ling Perman, Tuliana Cua, John Kauwe, John Allen, Henry M. Taylor, Kathryn Robson, Charlotte M. Deane, Andrew C. Steer, Adrian V. S. Hill, Lori Allen, M. David Allen, Corinne Braunstein, Samantha Colquhoun, Aurélia Jewine, Maureen Ah Kee, R. Uday Kumar, Martin Wj, Reapi L. Mataika, Marie Nadra, Shahin Nadu, Take Naseri, Baptiste Noël, Nathalie Simon, Brenton Ward

    Wydane 2017
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  8. 8
    A loss-of-function <i>IFNAR1</i> allele in Polynesia underlies severe viral diseases in homozygotes

    A loss-of-function <i>IFNAR1</i> allele in Polynesia underlies severe viral diseases in homozygotes od Paul Bastard, Kuang‐Chih Hsiao, Qian Zhang, Jérémy Choin, Emma Best, Jie Chen, Adrian Gervais, Lucy Bizien, Marie Materna, Christine Harmant, Maguelonne Roux, Nicola L. Hawley, Daniel E. Weeks, Stephen T. McGarvey, Karla Sandoval, Carmina Barberena-Jonas, Consuelo D. Quinto-Cortés, Erika Hagelberg, Alexander J. Mentzer, Kathryn Robson, Boubacar Coulibaly, Yoann Seeleuthner, Benedetta Bigio, Zhi Li, Gilles Uzé, Sandra Pellegrini, Lazaro Lorenzo, Zineb Sbihi, Sylvain Latour, Marianne Besnard, Tiphaine Adam de Beaumais, Evelyne Jacqz‐Aigrain, Vivien Béziat, Ranjan Deka, Litara Esera Tulifau, Satupaitea Viali, Muagututi‘a Sefuiva Reupena, Take Naseri, Peter McNaughton, Vanessa Sarkozy, Jane Peake, Annaliesse Blincoe, Sarah Primhak, Simon Stables, Kate Gibson, See‐Tarn Woon, Kylie M. Drake, Adrian V. S. Hill, Cheng-Yee Chan, Richard King, Rohan Ameratunga, Iotefa Teiti, Maïté Aubry, Van‐Mai Cao‐Lormeau, Stuart G. Tangye, Shen‐Ying Zhang, Emmanuelle Jouanguy, Paul Gray, Laurent Abel, Andrés Moreno‐Estrada, Ryan L. Minster, Lluı́s Quintana-Murci, Andrew Wood, Jean‐Laurent Casanova

    Wydane 2022
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  9. 9
    Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

    Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height od Gareth Hawkes, Robin N. Beaumont, Zilin Li, Ravi Mandla, Xihao Li, Christine M. Albert, Donna K. Arnett, Allison E. Ashley‐Koch, Aneel A. Ashrani, Kathleen C. Barnes, Eric Boerwinkle, Jennifer A. Brody, April P. Carson, Nathalie Chami, Yii‐Der Ida Chen, Mina K. Chung, Joanne E. Curran, Dawood Darbar, Patrick T. Ellinor, Myrian Fornage, Victor R. Gordeuk, Xiuqing Guo, Jiang He, Chii‐Min Hwu, Rita R. Kalyani, Robert C. Kaplan, Sharon Kardia, Charles Kooperberg, Ruth J. F. Loos, Steven A. Lubitz, Ryan L. Minster, Take Naseri, Satupaitea Viali, Braxton D. Mitchell, Joanne M. Murabito, Colin N. A. Palmer, Bruce M. Psaty, Susan Redline, M. Benjamin Shoemaker, Edwin K. Silverman, Marilyn J. Telen, Scott T. Weiss, Lisa R. Yanek, Hufeng Zhou, Yongmei Liu, Kari E. North, Anne E. Justice, Jonathan M. Locke, Nick Owens, Anna Murray, Kashyap Patel, Timothy M. Frayling, Caroline F. Wright, Andrew R. Wood, Xihong Lin, Alisa K. Manning, Michael N. Weedon

    Wydane 2024
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  10. 10
    A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

    A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies od Zilin Li, Xihao Li, Hufeng Zhou, Sheila M. Gaynor, Margaret Sunitha Selvaraj, Theodore Arapoglou, Corbin Quick, Yaowu Liu, Han Chen, Ryan Sun, Rounak Dey, Donna K. Arnett, Paul L. Auer, Lawrence F. Bielak, Joshua C. Bis, Thomas W. Blackwell, John Blangero, Eric Boerwinkle, Donald W. Bowden, Jennifer A. Brody, Brian E. Cade, Matthew P. Conomos, Adolfo Correa, L. Adrienne Cupples, Joanne E. Curran, Paul S. de Vries, Ravindranath Duggirala, Nora Franceschini, Barry I. Freedman, Harald H.H. Göring, Xiuqing Guo, Rita R. Kalyani, Charles Kooperberg, Brian G. Kral, Leslie A. Lange, Bridget M. Lin, Ani Manichaikul, Alisa K. Manning, Lisa W. Martin, Rasika A. Mathias, James B. Meigs, Braxton D. Mitchell, May E. Montasser, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Colin N. A. Palmer, Patricia A. Peyser, Bruce M. Psaty, Laura M. Raffield, Susan Redline, Alexander P. Reiner, Muagututi‘a Sefuiva Reupena, Kenneth Rice, Stephen S. Rich, Jennifer A. Smith, Kent D. Taylor, Margaret A. Taub, Ramachandran S. Vasan, Daniel E. Weeks, James G. Wilson, Lisa R. Yanek, Wei Zhao, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Nathan R. Blue, Russell P. Bowler, Ulrich Broeckel, Jai Broome, Deborah Brown

    Wydane 2022
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  11. 11
    Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

    Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies od Xihao Li, Corbin Quick, Hufeng Zhou, Sheila M. Gaynor, Yaowu Liu, Han Chen, Margaret Sunitha Selvaraj, Ryan Sun, Rounak Dey, Donna K. Arnett, Lawrence F. Bielak, Joshua C. Bis, John Blangero, Eric Boerwinkle, Donald W. Bowden, Jennifer A. Brody, Brian E. Cade, Adolfo Correa, L. Adrienne Cupples, Joanne E. Curran, Paul S. de Vries, Ravindranath Duggirala, Barry I. Freedman, Harald H.H. Göring, Xiuqing Guo, Jeffrey Haessler, Rita R. Kalyani, Charles Kooperberg, Brian G. Kral, Leslie A. Lange, Ani Manichaikul, Lisa W. Martin, Stephen T. McGarvey, Braxton D. Mitchell, May E. Montasser, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Colin N. A. Palmer, Patricia A. Peyser, Bruce M. Psaty, Laura M. Raffield, Susan Redline, Alexander P. Reiner, Muagututi‘a Sefuiva Reupena, Kenneth Rice, Stephen S. Rich, Colleen M. Sitlani, Jennifer A. Smith, Kent D. Taylor, Ramachandran S. Vasan, Cristen J. Willer, James G. Wilson, Lisa R. Yanek, Wei Zhao, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Thomas W. Blackwell, Nathan R. Blue, Russell P. Bowler, Ulrich Broeckel, Jai Broome, Deborah Brown, Karen Bunting, Esteban G. Burchard, Carlos D. Bustamante, Erin Buth, Jonathan Cardwell, Vincent J. Carey

    Wydane 2022
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  12. 12
    Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing

    Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing od Fang Chen, Xingyan Wang, Seon-Kyeong Jang, Bryan C. Quach, J. Dylan Weissenkampen, Chachrit Khunsriraksakul, Li‐Na Yang, Renan Sauteraud, Christine M. Albert, Nicholette D. Allred, Donna K. Arnett, Allison E. Ashley‐Koch, Kathleen C. Barnes, R. Graham Barr, Diane M. Becker, Lawrence F. Bielak, Joshua C. Bis, John Blangero, Meher Preethi Boorgula, Daniel I. Chasman, Sameer Chavan, Yii‐Der I. Chen, Lee‐Ming Chuang, Adolfo Correa, Joanne E. Curran, Sean P. David, Lisa de las Fuentes, Ranjan Deka, Ravindranath Duggirala, Jessica D. Faul, Melanie E. Garrett, Sina A. Gharib, Xiuqing Guo, Michael E. Hall, Nicola L. Hawley, Jiang He, Brian D. Hobbs, John E. Hokanson, Chao A. Hsiung, Shih‐Jen Hwang, Thomas M. Hyde, Marguerite R. Irvin, Andrew E. Jaffe, Eric O. Johnson, Robert C. Kaplan, Sharon L. R. Kardia, Joel D. Kaufman, Tanika N. Kelly, Joel E. Kleinman, Charles Kooperberg, I‐Te Lee, Daniel Levy, Sharon M. Lutz, Ani Manichaikul, Lisa W. Martin, Olivia Marx, Stephen T. McGarvey, Ryan L. Minster, Matthew Moll, Karine A. Moussa, Take Naseri, Kari E. North, Elizabeth C. Oelsner, Juan M. Peralta, Patricia A. Peyser, Bruce M. Psaty, Nicholas Rafaels, Laura M. Raffield, Muagututi‘a Sefuiva Reupena, Stephen S. Rich, Jerome I. Rotter, David A. Schwartz, Aladdin H. Shadyab, Wayne H-H Sheu, Mario Sims, Jennifer A. Smith, Xiao Sun, Kent D. Taylor, Marilyn J. Telen, Harold Watson, Daniel E. Weeks, David R. Weir, Lisa R. Yanek, Kendra A. Young, Kristin L. Young, Wei Zhao, Dana B. Hancock, Bibo Jiang, Scott Vrieze, Dajiang J. Liu

    Wydane 2023
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  13. 13
    Novel genetic determinants of telomere length from a trans-ethnic analysis of 109,122 whole genome sequences in TOPMed

    Novel genetic determinants of telomere length from a trans-ethnic analysis of 109,122 whole genome sequences in TOPMed od Margaret A. Taub, Matthew P. Conomos, Rebecca Keener, Kruthika Iyer, Joshua S. Weinstock, Lisa R. Yanek, John Lane, Tyne W. Miller‐Fleming, Jennifer A. Brody, Caitlin McHugh, Deepti Jain, Stephanie M. Gogarten, Cecelia Laurie, Ali R. Keramati, Marios Arvanitis, Albert V. Smith, Ben Heavner, Lucas Barwick, Lewis C. Becker, Joshua C. Bis, John Blangero, Eugene R. Bleecker, Esteban G. Burchard, Juan C. Celedón, Yen Chang, Brian Custer, Dawood Darbar, Lisa de las Fuentes, Dawn L. DeMeo, Barry I. Freedman, Melanie E. Garrett, Mark T. Gladwin, Susan R. Heckbert, Bertha Hidalgo, Marguerite R. Irvin, Talat Islam, W. Craig Johnson, Stefan Kääb, Lenore Launer, Jiwon Lee, Simin Liu, Arden Moscati, Kari E. North, Patricia A. Peyser, Nicholas Rafaels, Laura M. Raffield, Christine E. Seidman, Daniel E. Weeks, Fayuan Wen, Marsha M. Wheeler, L. Keoki Williams, Ivana V. Yang, Wei Zhao, Stella Aslibekyan, Paul L. Auer, Donald W. Bowden, Brian E. Cade, Zhanghua Chen, Michael H. Cho, L Adrienne Cupples, Joanne E. Curran, Michelle Daya, Ranjan Deka, Celeste Eng, Tasha E. Fingerlin, Xiuqing Guo, Lifang Hou, Shih‐Jen Hwang, Jill M. Johnsen, Eimear E. Kenny, Albert M. Levin, Chunyu Liu, Ryan L. Minster, Take Naseri, Mehdi Nouraie, Muagututi‘a Sefuiva Reupena, Éster Cerdeira Sabino, Jennifer A. Smith, Nicholas L. Smith, Jessica Lasky‐Su, Taylor James G, Marilyn J. Telen, Hemant K. Tiwari, Russell P. Tracy, Marquitta J. White, Yingze Zhang, Kerri L. Wiggins, Scott T. Weiss, Ramachandran S. Vasan, Kent D. Taylor, Moritz F. Sinner, Edwin K. Silverman, M. Benjamin Shoemaker, Wayne H-H Sheu, Frank C. Sciurba, David A. Schwartz, Jerome I. Rotter, Daniel Roden, Susan Redline, Benjamin A. Raby

    Wydane 2019
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  14. 14
    Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

    Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed od Margaret A. Taub, Matthew P. Conomos, Rebecca Keener, Kruthika Iyer, Joshua S. Weinstock, Lisa R. Yanek, John Lane, Tyne W. Miller‐Fleming, Jennifer A. Brody, Laura M. Raffield, Caitlin McHugh, Deepti Jain, Stephanie M. Gogarten, Cecelia Laurie, Ali R. Keramati, Marios Arvanitis, Albert V. Smith, Ben Heavner, Lucas Barwick, Lewis C. Becker, Joshua C. Bis, John Blangero, Eugene R. Bleecker, Esteban G. Burchard, Juan C. Celedón, Yen Chang, Brian Custer, Dawood Darbar, Lisa de las Fuentes, Dawn L. DeMeo, Barry I. Freedman, Melanie E. Garrett, Mark T. Gladwin, Susan R. Heckbert, Bertha Hidalgo, Marguerite R. Irvin, Talat Islam, W. Craig Johnson, Stefan Kääb, Lenore Launer, Jiwon Lee, Simin Liu, Arden Moscati, Kari E. North, Patricia A. Peyser, Nicholas Rafaels, Christine E. Seidman, Daniel E. Weeks, Fayuan Wen, Marsha M. Wheeler, L. Keoki Williams, Ivana V. Yang, Wei Zhao, Stella Aslibekyan, Paul L. Auer, Donald W. Bowden, Brian E. Cade, Zhanghua Chen, Michael H. Cho, L. Adrienne Cupples, Joanne E. Curran, Michelle Daya, Ranjan Deka, Celeste Eng, Tasha E. Fingerlin, Xiuqing Guo, Lifang Hou, Shih‐Jen Hwang, Jill M. Johnsen, Eimear E. Kenny, Albert M. Levin, Chunyu Liu, Ryan L. Minster, Take Naseri, Mehdi Nouraie, Muagututi‘a Sefuiva Reupena, Éster Cerdeira Sabino, Jennifer A. Smith, Nicholas L. Smith, Jessica Lasky‐Su, James G. Taylor, Marilyn J. Telen, Hemant K. Tiwari, Russell P. Tracy, Marquitta J. White, Yingze Zhang, Kerri L. Wiggins, Scott T. Weiss, Ramachandran S. Vasan, Kent D. Taylor, Moritz F. Sinner, Edwin K. Silverman, M. Benjamin Shoemaker, Wayne H.-H. Sheu, Frank C. Sciurba, David A. Schwartz, Jerome I. Rotter, Daniel Roden, Susan Redline, Benjamin A. Raby

    Wydane 2022
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  15. 15
    Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

    Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential od Tetsushi Nakao, Alexander G. Bick, Margaret A. Taub, Seyedeh M. Zekavat, Md Mesbah Uddin, Abhishek Niroula, Cara L. Carty, John Lane, Michael C. Honigberg, Joshua S. Weinstock, Akhil Pampana, Christopher J. Gibson, Gabriel K. Griffin, Shoa L. Clarke, Romit Bhattacharya, Themistocles L. Assimes, Leslie Emery, Adrienne M. Stilp, Quenna Wong, Jai Broome, Cecelia Laurie, Alyna Khan, Albert V. Smith, Thomas W. Blackwell, Veryan Codd, Christopher P. Nelson, Zachary T. Yoneda, Juan M. Peralta, Donald W. Bowden, Marguerite R. Irvin, Meher Preethi Boorgula, Wei Zhao, Lisa R. Yanek, Kerri L. Wiggins, James E. Hixson, C. Charles Gu, Gina M. Peloso, Dan M. Roden, Muagututi‘a Sefuiva Reupena, Chii‐Min Hwu, Dawn L. DeMeo, Kari E. North, Shannon Kelly, Solomon K. Musani, Joshua C. Bis, Donald M. Lloyd‐Jones, Jill M. Johnsen, Michael Preuß, Russell P. Tracy, Patricia A. Peyser, Dandi Qiao, Pinkal Desai, Joanne E. Curran, Barry I. Freedman, Hemant K. Tiwari, Sameer Chavan, Jennifer A. Smith, Nicholas L. Smith, Tanika N. Kelly, Bertha Hidalgo, L. Adrienne Cupples, Daniel E. Weeks, Nicola L. Hawley, Ryan L. Minster, Ranjan Deka, Take Naseri, Lisa de las Fuentes, Laura M. Raffield, Alanna C. Morrison, Paul S. de Vries, Christie M. Ballantyne, Eimear E. Kenny, Stephen S. Rich, Eric A. Whitsel, Michael H. Cho, M. Benjamin Shoemaker, Betty S. Pace, John Blangero, Colin N. A. Palmer, Braxton D. Mitchell, Alan R. Shuldiner, Kathleen C. Barnes, Susan Redline, Sharon L.R. Kardia, Gonçalo R. Abecasis, Lewis C. Becker, Susan R. Heckbert, Jiang He, Wendy S. Post, Donna K. Arnett, Ramachandran S. Vasan, Dawood Darbar, Scott T. Weiss, Stephen T. McGarvey, Mariza de Andrade, Yii‐Der Ida Chen, Robert C. Kaplan, Deborah A. Meyers, Brian Custer, Adolfo Correa

    Wydane 2022
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  16. 16
    Whole genome sequence analysis of blood lipid levels in &gt;66,000 individuals

    Whole genome sequence analysis of blood lipid levels in &gt;66,000 individuals od Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, Akhil Pampana, David Zhang, Joseph Park, Stella Aslibekyan, Joshua C. Bis, Jennifer A. Brody, Brian E. Cade, Lee‐Ming Chuang, Ren‐Hua Chung, Joanne E. Curran, Lisa de las Fuentes, Paul S. de Vries, Ravindranath Duggirala, Barry I. Freedman, Mariaelisa Graff, Xiuqing Guo, Nancy L. Heard‐Costa, Bertha Hidalgo, Chii‐Min Hwu, Marguerite R. Irvin, Tanika N. Kelly, Brian G. Kral, Leslie A. Lange, Xiaohui Li, Martin Lisa, Steven A. Lubitz, Ani Manichaikul, Michael Preuß, May E. Montasser, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Colin N. A. Palmer, Patricia A. Peyser, Muagututi‘a Sefuiva Reupena, Jennifer A. Smith, Xiao Sun, Kent D. Taylor, Russell P. Tracy, Michael Y. Tsai, Zhe Wang, Yuxuan Wang, Wei Bao, John T. Wilkins, Lisa R. Yanek, Wei Zhao, Donna K. Arnett, John Blangero, Eric Boerwinkle, Donald W. Bowden, Yii‐Der Ida Chen, Adolfo Correa, L. Adrienne Cupples, Susan K. Dutcher, Patrick T. Ellinor, Myriam Fornage, Stacey Gabriel, Søren Germer, Richard A. Gibbs, Jiang He, Robert C. Kaplan, Sharon L. R. Kardia, Ryan Kim, Charles Kooperberg, Ruth J. F. Loos, Karine A. Viaud‐Martinez, Rasika A. Mathias, Stephen T. McGarvey, Braxton D. Mitchell, Deborah A. Nickerson, Kari E. North, Bruce M. Psaty, Susan Redline, Alexander P. Reiner, Ramachandran S. Vasan, Stephen S. Rich, Cristen J. Willer, Jerome I. Rotter, Daniel J. Rader, Xihong Lin, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas

    Wydane 2022
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  17. 17
    Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele

    Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele od Xinruo Zhang, Jennifer A. Brody, Mariaelisa Graff, Heather M. Highland, Nathalie Chami, Hanfei Xu, Zhe Wang, Kendra Ferrier, Geetha Chittoor, Navya Shilpa Josyula, Mariah Meyer, Shreyash Gupta, Xihao Li, Zilin Li, Matthew Allison, Diane M. Becker, Lawrence F. Bielak, Joshua C. Bis, Meher Preethi Boorgula, Donald W. Bowden, Jai Broome, Erin Buth, Christopher S. Carlson, Kyong–Mi Chang, Sameer Chavan, Yen‐Feng Chiu, Lee‐Ming Chuang, Matthew P. Conomos, Dawn L. DeMeo, Mengmeng Du, Ravindranath Duggirala, Celeste Eng, Alison E. Fohner, Barry I. Freedman, Melanie E. Garrett, Xiuqing Guo, Chris Haiman, Ben Heavner, Bertha Hidalgo, James E. Hixson, Yuk‐Lam Ho, Brian D. Hobbs, Donglei Hu, Qin Hui, Chii‐Min Hwu, Rebecca D. Jackson, Deepti Jain, Rita R. Kalyani, Sharon L.R. Kardia, Tanika N. Kelly, Ethan M. Lange, Michael A. LeNoir, Changwei Li, Loı̈c Le Marchand, Merry‐Lynn McDonald, Caitlin McHugh, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Christopher J O'Donnell, Nicholette D. Allred, James S. Pankow, James A. Perry, Ulrike Peters, Michael Preuß, D. C. Rao, Elizabeth A. Regan, Sefuiva M Reupena, Dan M. Roden, José Rodríguez‐Santana, Colleen M. Sitlani, Jennifer A. Smith, Hemant K. Tiwari, Ramachandran S. Vasan, Zeyuan Wang, Daniel E. Weeks, Jennifer Wessel, Kerri L. Wiggins, Lynne R. Wilkens, Peter W.F. Wilson, Lisa R. Yanek, Zachary T. Yoneda, Wei Zhao, Sebastian Zöllner, Donna K. Arnett, Allison E. Ashley‐Koch, Kathleen C. Barnes, John Blangero, Eric Boerwinkle, Esteban G. Burchard, April P. Carson, Daniel I. Chasman, Yii‐Der Ida Chen, Joanne E. Curran, Myriam Fornage, Victor R. Gordeuk, Jiang He, Susan R. Heckbert, Lifang Hou, Marguerite R. Irvin

    Wydane 2025
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