Zobrazeno 71 - 80
of 127
pro vyhledávání: '"Jennifer, E Below"'
Autor:
Jennifer E. Below, Andrew D. Morris, Kyle J. Gaulton, Weihua Zhang, Anubha Mahajan, Xueling Sim, Maggie Ng, Hidetoshi Kitajima, Anthony Payne
Publikováno v:
Diabetes. 67
To discover type 2 diabetes (T2D) loci and enhance fine-mapping resolution, we conducted the largest meta-analysis of genome-wide association studies of the disease to date by aggregating 171,262 cases and 1,075,072 controls from diverse populations
Autor:
Sanjay R. Patel, Elizabeth Barrett-Connor, Xiuqing Guo, Heming Wang, Katie L. Stone, Scott A. Sands, Raanan Arens, Han Chen, Alexis C. Wood, Kristine Yaffe, Xihong Lin, James G. Wilson, Brian E. Cade, Tamar Sofer, Xiaofeng Zhu, Shaun Purcell, Tin Louie, Jerome I. Rotter, Shamil R. Sunyaev, Gregory J. Tranah, Richa Saxena, Adrienne M. Stilp, Phyllis C. Zee, Alberto R. Ramos, Kent D. Taylor, Jose S. Loredo, Jianwen Cai, Timothy A. Thornton, Neomi A. Shah, Cathy C. Laurie, W. Craig Johnson, Craig L. Hanis, Daniel J. Gottlieb, Sina A. Gharib, Jennifer E. Below, Matthew P. Conomos, Sonia Ancoli-Israel, Wendy S. Post, Sharon R. Browning, Susan Redline, Kenneth Rice, Daniel S. Evans, Hao Mei
Publikováno v:
Human molecular genetics, vol 28, iss 4
Obstructive sleep apnea (OSA) is a common disorder associated with increased risk of cardiovascular disease and mortality. Its prevalence and severity vary across ancestral background. Although OSA traits are heritable, few genetic associations have
Autor:
Amy S. Bruckman, Jennifer E. Below, Lucas Dixon, Casey Fiesler, Eric E. Gilbert, Sarah A. Gilbert, J. Nathan Matias
Publikováno v:
Extended Abstracts of the 2018 CHI Conference on Human Factors in Computing Systems.
Autor:
Wendy S. Post, Jose S. Loredo, Shaun Purcell, Gregory J. Tranah, Craig L. Hanis, James G. Wilson, Matthew P. Conomos, Sonia Ancoli-Israel, Shamil R. Sunyaev, Sina A. Gharib, Katie L. Stone, Timothy A. Thornton, Kent D. Taylor, W. Craig Johnson, Phyllis C. Zee, Richard Barfield, Kathryn J. Reid, Adrienne M. Stilp, Raanan Arens, Han Chen, David J. Lederer, Sanjay R. Patel, Kenneth Rice, Kristine Yaffe, Tin Louie, Kevin J. Gleason, Daniel S. Evans, Alexis C. Frazier-Wood, Hao Mei, Jerome I. Rotter, Neomi Shah, Jiwon Lee, Richa Saxena, Xiaofeng Zhu, Lyle J. Palmer, Alberto R. Ramos, Cathy C. Laurie, Susan Redline, Brian E. Cade, Tamar Sofer, David R. Hillman, Heming Wang, Jianwen Cai, Xihong Lin, Daniel J. Gottlieb, Sutapa Mukherjee, Jennifer E. Below
Publikováno v:
PLoS genetics, vol 15, iss 4
Sleep disordered breathing (SDB)-related overnight hypoxemia is associated with cardiometabolic disease and other comorbidities. Understanding the genetic bases for variations in nocturnal hypoxemia may help understand mechanisms influencing oxygenat
Autor:
Nancy J. Cox, Jennifer E. Below
Publikováno v:
Circulation research. 122(8)
The rampant misuse of the P value and of its stated meaning lead the American Statistical Association to comment, researchers often wish to turn a P value into a statement about the truth of a null hypothesis, or about the probability that random cha
Autor:
Elena V. Feofanova, Bing Yu, Ginger A. Metcalf, Richard A. Gibbs, Lynne E. Wagenknecht, Xiaoming Liu, Jennifer E. Below, Alanna C. Morrison, Eric Boerwinkle, Donna M. Muzny
Small molecule lipid-related metabolites are important components of fatty acid and steroid metabolism—two important contributors to human health. This study investigated the extent to which rare and common genetic variants spanning the human genom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09d71c6ddffaaeb07f2679286f7b1cb8
https://europepmc.org/articles/PMC5972430/
https://europepmc.org/articles/PMC5972430/
Autor:
Matthew P. Conomos, Sonia Ancoli-Israel, Simon C. Warby, Beate Stubbe, Phyllis C. Zee, W. Craig Johnson, Xihong Lin, Adrienne M. Stilp, Neomi A. Shah, Daniel J. Gottlieb, Thomas Penzel, Seung Ku Lee, Scott A. Sands, Richa Saxena, Chaolong Wang, Xiaofeng Zhu, Cathy C. Laurie, Zoltán Kutalik, Andrew Bjonnes, Jingjing Liang, Graeme I. Bell, D. Andrew Wellman, Raanan Arens, Susan Redline, Lyle J. Palmer, Alexander Teumer, Kevin J. Gleason, Kent D. Taylor, Emma K. Larkin, Erika W. Hagen, Gregory J. Tranah, Mehdi Tafti, George J. Papanicolaou, Kenneth Rice, Sanjay R. Patel, David R. Hillman, Craig L. Hanis, Chol Shin, Sutapa Mukherjee, Daniel S. Evans, Jerome I. Rotter, Ralf Ewert, Jennifer E. Below, Wendy S. Post, Brian E. Cade, Tamar Sofer, Sina A. Gharib, Raphael Heinzer, Jae Hoon Sul, Sung Chun, Han Chen, Alexis C. Frazier-Wood, Jacqueline M. Lane, José Haba-Rubio, Heming Wang, Timothy A. Thornton, Jose S. Loredo, Alberto R. Ramos, Ali Azarbarzin, Shamil R. Sunyaev, Katie L. Stone, Paul E. Peppard
Publikováno v:
American journal of respiratory cell and molecular biology, vol. 58, no. 3, pp. 391-401
American journal of respiratory cell and molecular biology, vol 58, iss 3
American journal of respiratory cell and molecular biology, vol 58, iss 3
Obstructive sleep apnea (OSA) is a common heritable disorder displaying marked sexual dimorphism in disease prevalence and progression. Previous genetic association studies have identified a few genetic loci associated with OSA and related quantitati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3ffcb9b8efdc75ec6d8608da58d9c65
https://europepmc.org/articles/PMC5854957/
https://europepmc.org/articles/PMC5854957/
Autor:
Esteban J. Parra, Annie Green Howard, Struan F.A. Grant, Carmen R. Isasi, Jennifer E. Below, Ruth J. F. Loos, Qibin Qi, Kristin L. Young, Cathy C. Laurie, Robert C. Kaplan, Mariaelisa Graff, Anne E. Justice, Kari E. North, Christopher A. Haiman, Heather M. Highland, George Papanicolaou, Lindsay Fernández-Rhodes
Publikováno v:
BMC Obesity
BMC Obesity, Vol 5, Iss 1, Pp 1-12 (2018)
BMC Obesity, Vol 5, Iss 1, Pp 1-12 (2018)
Background Genome-wide association studies have implicated the transcription factor 7-like 2 (TCF7L2) gene in type 2 diabetes risk, and more recently, in decreased body mass index. Given the contrary direction of genetic effects on these two traits,
Autor:
Mamdouh Aker, Brent L. Fogel, Kathie J. Ngo, Jason Chen, Michael D. Geschwind, Susan Perlman, Sebastiano Cavallaro, S. Hassin-Baer, Lauren E. Petty, Angelina Laganà, Giovanni Coppola, Jennifer E. Below, Francesca Cavalcanti, Domenico Italiano, Alexandra B. Nelson
Publikováno v:
Neurology: Genetics Jun 4 (2018): 1–3. doi:10.1212/NXG.0000000000000232
info:cnr-pdr/source/autori:Kathie Ngo, Mamdouh Aker, Lauren E. Petty, Jason Chen, Francesca Cavalcanti, Alexandra B. Nelson, Sharon Hassin-Baer, Michael D. Geschwind, Susan Perlman, Domenico Italiano, Angelina Laganà, Sebastiano Cavallaro, Giovanni Coppola, Jennifer E. Below and Brent L. Fogel/titolo:Expanding the Global Prevalence of Spinocerebellar Ataxia Type 42/doi:10.1212%2FNXG.0000000000000232/rivista:Neurology: Genetics/anno:2018/pagina_da:1/pagina_a:3/intervallo_pagine:1–3/volume:Jun 4
Neurology: Genetics
info:cnr-pdr/source/autori:Kathie Ngo, Mamdouh Aker, Lauren E. Petty, Jason Chen, Francesca Cavalcanti, Alexandra B. Nelson, Sharon Hassin-Baer, Michael D. Geschwind, Susan Perlman, Domenico Italiano, Angelina Laganà, Sebastiano Cavallaro, Giovanni Coppola, Jennifer E. Below and Brent L. Fogel/titolo:Expanding the Global Prevalence of Spinocerebellar Ataxia Type 42/doi:10.1212%2FNXG.0000000000000232/rivista:Neurology: Genetics/anno:2018/pagina_da:1/pagina_a:3/intervallo_pagine:1–3/volume:Jun 4
Neurology: Genetics
Spinocerebellar ataxias (SCAs) are a heterogeneous group of neurodegenerative disorders that involve the degeneration of the cerebellum and brainstem.1 These genetic diseases are characterized by autosomal dominant inheritance with approximately 44 k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d42eec0228bb4c6165952a64e5c9c9dd
http://hdl.handle.net/11570/3126131
http://hdl.handle.net/11570/3126131
Autor:
William J Salerno, Christiane Reitz, Josée Dupuis, Richard Mayeux, Sudha Seshadri, Badri N. Vardarajan, Gerard D. Schellenberg, Lindsay A. Farrer, Elizabeth E. Blue, Ellen M. Wijsman, Dolly Reyes, Harkirat Sohi, Kathryn L. Lunetta, Yiyi Ma, Otto Valadares, Eden R. Martin, Sandra Barral, Anita L. DeStefano, Carlos Cruchaga, Eric Boerwinkle, Joshua C. Bis, Li-San Wang, Gyungah Jun, Alison Goate, Mariusz Butkiewicz, Jenny Lee, Patrick A. Navas, Margaret A. Pericak-Vance, Michael O. Dorschner, Gary W. Beecham, William S. Bush, Jennifer E. Below, Timothy A. Thornton, Brian W. Kunkle, Alejandro Q. Nato, Adam C. Naj, Jim Jaworski, Amanda B. Kuzma, Debby W. Tsuang, Hiep Nguyen, Cornelia M. van Duijn, Jonathan L. Haines
Publikováno v:
Dementia and Geriatric Cognitive Disorders, 45(1-2), 1-17. Karger
Background/Aims: The Alzheimer’s Disease Sequencing Project (ADSP) aims to identify novel genes influencing Alzheimer’s disease (AD). Variants within genes known to cause dementias other than AD have previously been associated with AD risk. We de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0f672981e1f5efcc530686988a84fb0
https://pure.eur.nl/en/publications/0e86eced-70dc-4029-a9e0-ab30464a76de
https://pure.eur.nl/en/publications/0e86eced-70dc-4029-a9e0-ab30464a76de