Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Jennifer, E Below"'
Autor:
Lauren E. Petty, Hannah P. Polikowsky, Dillon G. Pruett, Robin M. Jones, Kathryn Z. Viljoen, Shelly Jo Kraft, Hung-Hsin Chen, Jennifer E. Below, Janet M. Beilby, Douglas M. Shaw
Publikováno v:
American Journal of Human Genetics
Summary Developmental stuttering is a speech disorder characterized by disruption in the forward movement of speech. This disruption includes part-word and single-syllable repetitions, prolongations, and involuntary tension that blocks syllables and
Autor:
Kathrine M Phillippi-Falkenstein, Lauren E. Petty, Rudolf P. Bohm, Jeffrey Rogers, Chad D. Huff, R. Alan Harris, Eric J. Vallender, H. Michael Kubisch, Muthuswamy Raveendran, Jennifer E. Below
Publikováno v:
Molecular Ecology Resources
A primary challenge in the analysis of free‐ranging animal populations is the accurate estimation of relatedness among individuals. Many aspects of population analysis rely on knowledge of relatedness patterns, including socioecology, demography, h
Autor:
Kathryn Z. Viljoen, Heather M. Highland, Lauren E. Petty, Jonathon P. Linklater, Brandt Levitt, Jennifer E. Below, Dillon G. Pruett, Douglas M. Shaw, Kathleen Mullan Harris, Hannah G. Polikowsky, Shelly Jo Kraft, Robin M. Jones, Hung-Hsin Chen, Janet M. Beilby, Christy L. Avery
Publikováno v:
HGG Advances, Vol 3, Iss 1, Pp 100073-(2022)
Human Genetics and Genomics Advances
Human Genetics and Genomics Advances
Summary Despite a lifetime prevalence of at least 5%, developmental stuttering, characterized by prolongations, blocks, and repetitions of speech sounds, remains a largely idiopathic speech disorder. Family, twin, and segregation studies overwhelming
Autor:
Ernest T. Hawk, Jianhua Zhang, Laura Beretta, Xiaogang Wu, Joseph B. McCormick, P. Andrew Futreal, Aron Y. Joon, Suet-Ying Kwan, Susan P. Fisher-Hoch, Jingjing Jiao, Robert R. Jenq, Jennifer E. Below, Carrie R. Daniel, Lauren E. Petty, Peng Wei
Publikováno v:
Hepatology
Background and aims Hispanics are disproportionately affected by non-alcoholic fatty liver disease, liver fibrosis, cirrhosis, and hepatocellular carcinoma. Preventive strategies and non-invasive means to identify those in this population at high ris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4e898ee6b8dc45ecccf1ba9c8eaa198
https://europepmc.org/articles/PMC8930512/
https://europepmc.org/articles/PMC8930512/
Autor:
Eric Boerwinkle, Lisa R. Yanek, Teresa Tusié-Luna, Lynne R. Wikens, Charles Kooperberg, Richard A. Jensen, Ruth J. F. Loos, Ping An, Xin Sheng, Lauren E. Petty, Yingchang Lu, Girish N. Nadkarni, Martha L. Daviglus, Suhn K. Rhie, Pierre Fontanillas, Lawrence S. Phillips, Cassandra N. Spracklen, Wei-Min Chen, Jennifer E. Below, Maggie C.Y. Ng, Yoonjung Yoonie Joo, Aude Nicolas, Stephanie A. Bien, Mariaelisa Graff, Qibin Qi, Burcu F. Darst, Lawrence F. Bielak, Kari E. North, Salman M. Tajuddin, Brian E. Cade, Christopher A. Haiman, Xueling Sim, Linda M. Polfus, Loic Le Marchand, Steven Buyske, Heather M. Highland, Lorena Orozco, James S. Pankow, Ulrike Peters, Meng Sun, Xiuqing Guo, Michael Preuss, Yesha Patel, Laura M. Raffield, Joseph M. Mercader, Simin Liu, Christopher S. Carlson, Guanjie Chen, Zhaohui Du, Clicerio González-Villalpando, Daniel O. Stram, Ran Tao, Wei Wang, Claudia Schurmann
Publikováno v:
HGG advances
HGG Advances, Vol 2, Iss 2, Pp 100029-(2021)
HGG Advances, Vol 2, Iss 2, Pp 100029-(2021)
Summary: Genomic discovery and characterization of risk loci for type 2 diabetes (T2D) have been conducted primarily in individuals of European ancestry. We conducted a multiethnic genome-wide association study of T2D among 53,102 cases and 193,679 c
Autor:
Z. Oya Uyguner, Jennifer E. Posey, Ariadne Letra, Donna M. Muzny, Nuriye Dinckan, Eric Boerwinkle, Xiaofei Song, Nan Wu, Lauren E. Petty, Hülya Kayserili, Shalini N. Jhangiani, Renqian Du, Oya Aktören, James R. Lupski, Yeliz Güven, Richard A. Gibbs, Jennifer E. Below, Zeynep Coban-Akdemir
Publikováno v:
Human Genetics. 137:689-703
Tooth agenesis (TA), the failure of development of one or more permanent teeth, is a common craniofacial abnormality observed in different world populations. The genetic etiology of TA is heterogeneous; more than a dozen genes have been associated wi
Autor:
Martha L. Daviglus, Daniel J. Schaid, Jeffrey Haessler, Adolfo Correa, Iona Cheng, Austin T. Hilliard, Yingchang Lu, Ozan Dikilitas, Gail P. Jarvik, Stephanie A. Bien, Lynne R. Wilkens, Yao Hu, Patrick M. A. Sleiman, Ulrike Peters, Laura J. Rasmussen-Torvik, Frank D. Mentch, Christopher J. O'Donnell, Lauren E. Petty, Kari E. North, Mariaelisa Graff, Christopher A. Haiman, Loic Le Marchand, Marie Verbanck, Peter W.F. Wilson, Steven Buyske, Ruth J. F. Loos, QiPing Feng, VA Million Veteran Program, Tara C. Matise, Charles Kooperberg, Ron Do, Kelly Cho, Scott M. Damrauer, Iftikhar J. Kullo, Christopher S. Carlson, Jennifer E. Below, Berta Almoguera, Philip S. Tsao, Themistocles L. Assimes, Lisa W. Martin, Wei-Qi Wei, Yuk-Lam Ho, Eric B. Larson, Ran Tao, Lucia A. Hindorff, Katherine K. Nishimura, José Luis Ambite, Matthew L. Kosel, Kyong-Mi Chang, Derek Klarin, Daniel O. Stram, Laura M. Raffield, Niha Zubair, Heather M. Highland
Publikováno v:
PLoS Genetics, Vol 16, Iss 3, p e1008684 (2020)
PLoS Genetics
PLoS Genetics
Lipid levels are important markers for the development of cardio-metabolic diseases. Although hundreds of associated loci have been identified through genetic association studies, the contribution of genetic factors to variation in lipids is not full
Autor:
Dmitry Akhmedov, Richard A. Gibbs, Brent L. Fogel, Zuleima Yáñez, Jennifer E. Below, Juliana M. Valera, Rebecca Berdeaux, James R. Lupski, María Jesús Sobrido, Beatriz Quintáns, Susan Perlman, Tatyana Diaz, Eric Boerwinkle, Donna M. Muzny, Lauren E. Petty, Daniel H. Geschwind
Publikováno v:
Neurology: Genetics
Neurology. Genetics, vol 3, iss 4
Neurology. Genetics, vol 3, iss 4
Objective:To assess the prevalence and clinical features of individuals affected by spinocerebellar ataxia 36 (SCA36) at a large tertiary referral center in the United States.Methods:A total of 577 patients with undiagnosed sporadic or familial cereb
Autor:
Jacqueline M. Lane, Sung Chun, Kenneth Rice, Daniel S. Evans, Brian E. Cade, Tamar Sofer, Sonia Ancoli-Israel, Chaolong Wang, Xihong Lin, Gregory J. Tranah, Kent D. Taylor, Raanan Arens, Craig L. Hanis, Kevin J. Gleason, Jerome I. Rotter, Neomi A. Shah, Phyllis C. Zee, Cathy C. Laurie, Adrienne M. Stilp, W. Craig Johnson, Jennifer E. Below, Matthew P. Conomos, Wendy S. Post, Andrew Bjonnes, Richa Saxena, Han Chen, Graeme I. Bell, Emma K. Larkin, Sanjay R. Patel, Alexis C. Frazier-Wood, Xiaofeng Zhu, Susan Redline, Alberto R. Ramos, Jose S. Loredo, Timothy A. Thornton, Katie L. Stone, Shamil R. Sunyaev
Publikováno v:
American journal of respiratory and critical care medicine, vol 194, iss 7
Cade, BE; Chen, H; Stilp, AM; Gleason, KJ; Sofer, T; Ancoli-Israel, S; et al.(2016). Genetic associations with obstructive sleep apnea traits in Hispanic/Latino Americans. American Journal of Respiratory and Critical Care Medicine, 194(7), 886-897. doi: 10.1164/rccm.201512-2431OC. UCLA: Retrieved from: http://www.escholarship.org/uc/item/4v121439
Cade, BE; Chen, H; Stilp, AM; Gleason, KJ; Sofer, T; Ancoli-Israel, S; et al.(2016). Genetic associations with obstructive sleep apnea traits in Hispanic/Latino Americans. American Journal of Respiratory and Critical Care Medicine, 194(7), 886-897. doi: 10.1164/rccm.201512-2431OC. UCLA: Retrieved from: http://www.escholarship.org/uc/item/4v121439
Copyright © 2016 by the American Thoracic Society. Rationale: Obstructive sleep apnea is a common disorder associated with increased risk for cardiovascular disease, diabetes, and premature mortality. Although there is strong clinical and epidemiolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cd6448d6a692328a517ffdc0cc16aaa
https://escholarship.org/uc/item/4v121439
https://escholarship.org/uc/item/4v121439
Autor:
Ruth J. F. Loos, Ani W. Manichakul, Eric R. Gamazon, Kent D. Taylor, Craig L. Hanis, Esteban J. Parra, Adan Valladares-Salgado, Jerome I. Rotter, Hua Tang, Sophie I. Candille, Xin-Qun Wang, Miguel Cruz, Erwin P. Bottinger, Nancy J. Cox, Qing Duan, S. Krithika, Jesús Peralta-Romero, Yingchang Lu, Jason M. Torres, Jennifer E. Below, Andrew P. Morris, Stephen S. Rich, Yun Li, Omri Gottesman, Y.-D. Ida Chen
Publikováno v:
Scientific Reports
Scientific reports, vol 6, iss 1
Scientific reports, 6. Nature Publishing Group
Scientific reports, vol 6, iss 1
Scientific reports, 6. Nature Publishing Group
We performed genome-wide meta-analysis of lipid traits on three samples of Mexican and Mexican American ancestry comprising 4,383 individuals and followed up significant and highly suggestive associations in three additional Hispanic samples comprisi