Naturally occurring HCA1 missense mutations result in loss of function: potential impact on lipid deposition

Por Doyle, Jamie R., Lane, Jacqueline M., Beinborn, Martin, Kopin, Alan S.
Publicado em 2013

HUMAN SWI/SNF DRIVES SEQUENCE-DIRECTED REPOSITIONING OF NUCLEOSOMES ON C-MYC PROMOTER DNA MINICIRCLES

Por Sims, Hillel I., Lane, Jacqueline M., Ulyanova, Natalia P., Schnitzler, Gavin R.
Publicado em 2007

Development of an OP9 Derived Cell Line as a Robust Model to Rapidly Study Adipocyte Differentiation

Por Lane, Jacqueline M., Doyle, Jamie R., Fortin, Jean-Philippe, Kopin, Alan S., Ordovás, José M.
Publicado no PLoS One (2014)

The effects of ABCG5/G8 polymorphisms on HDL cholesterol concentrations depend on ABCA1 genetic variants in the Boston Puerto Rican Health Study

Por Junyent, Mireia, Tucker, Katherine L., Smith, Caren E., Lane, Jacqueline M., Mattei, Josiemer, Lai, Chao-Qiang, Parnell, Laurence D., Ordovas, Jose M.
Publicado em 2009

Common variants in CLOCK are not associated with measures of sleep duration in people of European ancestry from the Sleep Heart Health Study

Por Lane, Jacqueline M., Tare, Archana, Cade, Brian E., Chen, Ting-hsu, Punjabi, Naresh M., Gottlieb, Daniel J., Scheer, Frank A.J.L., Redline, Susan, Saxena, Richa
Publicado em 2013

CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids

Por Eichler, Florian S., Li, Jiankang, Guo, Yiran, Caruso, Paul A., Bjonnes, Andrew C., Pan, Jessica, Booker, Jessica K., Lane, Jacqueline M., Tare, Archana, Vlasac, Irma, Hakonarson, Hakon, Gusella, James F., Zhang, Jianguo, Keating, Brendan J., Saxena, Richa
Publicado no Brain (2016)

Sleep duration does not mediate or modify association of common genetic variants with type 2 diabetes

Por Tare, Archana, Lane, Jacqueline M., Cade, Brian E., Grant, Struan F. A., Chen, Ting-hsu, Punjabi, Naresh M., Lauderdale, Diane S., Zee, Phyllis C., Gharib, Sina A., Gottlieb, Daniel J., Scheer, Frank A. J. L., Redline, Susan, Saxena, Richa
Publicado em 2013

Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank

Por Lane, Jacqueline M., Vlasac, Irma, Anderson, Simon G., Kyle, Simon D., Dixon, William G., Bechtold, David A., Gill, Shubhroz, Little, Max A., Luik, Annemarie, Loudon, Andrew, Emsley, Richard, Scheer, Frank A. J. L., Lawlor, Deborah A., Redline, Susan, Ray, David W., Rutter, Martin K., Saxena, Richa
Publicado no Nat Commun (2016)

Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits

Por Lane, Jacqueline M., Liang, Jingjing, Vlasac, Irma, Anderson, Simon G., Bechtold, David A., Bowden, Jack, Emsley, Richard, Gill, Shubhroz, Little, Max A., Luik, AnneMarie I., Loudon, Andrew, Scheer, Frank A.J.L., Purcell, Shaun M., Kyle, Simon D., Lawlor, Deborah A., Zhu, Xiaofeng, Redline, Susan, Ray, David W., Rutter, Martin K., Saxena, Richa
Publicado no Nat Genet (2016)

Impact of Common Diabetes Risk Variant in MTNR1B on Sleep, Circadian, and Melatonin Physiology

Por Lane, Jacqueline M., Chang, Anne-Marie, Bjonnes, Andrew C., Aeschbach, Daniel, Anderson, Clare, Cade, Brian E., Cain, Sean W., Czeisler, Charles A., Gharib, Sina A., Gooley, Joshua J., Gottlieb, Daniel J., Grant, Struan F.A., Klerman, Elizabeth B., Lauderdale, Diane S., Lockley, Steven W., Munch, Miriam, Patel, Sanjay, Punjabi, Naresh M., Rajaratnam, Shanthakumar M.W., Rueger, Melanie, St. Hilaire, Melissa A., Santhi, Nayantara, Scheuermaier, Karin, Van Reen, Eliza, Zee, Phyllis C., Shea, Steven A., Duffy, Jeanne F., Buxton, Orfeu M., Redline, Susan, Scheer, Frank A.J.L., Saxena, Richa
Publicado no Diabetes (2016)

Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans

Por Cade, Brian E., Chen, Han, Stilp, Adrienne M., Gleason, Kevin J., Sofer, Tamar, Ancoli-Israel, Sonia, Arens, Raanan, Bell, Graeme I., Below, Jennifer E., Bjonnes, Andrew C., Chun, Sung, Conomos, Matthew P., Evans, Daniel S., Johnson, W. Craig, Frazier-Wood, Alexis C., Lane, Jacqueline M., Larkin, Emma K., Loredo, Jose S., Post, Wendy S., Ramos, Alberto R., Rice, Ken, Rotter, Jerome I., Shah, Neomi A., Stone, Katie L., Taylor, Kent D., Thornton, Timothy A., Tranah, Gregory J., Wang, Chaolong, Zee, Phyllis C., Hanis, Craig L., Sunyaev, Shamil R., Patel, Sanjay R., Laurie, Cathy C., Zhu, Xiaofeng, Saxena, Richa, Lin, Xihong, Redline, Susan
Publicado no Am J Respir Crit Care Med (2016)

Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations

Por Liang, Jingjing, Le, Thu H., Edwards, Digna R. Velez, Tayo, Bamidele O., Gaulton, Kyle J., Smith, Jennifer A., Lu, Yingchang, Jensen, Richard A., Chen, Guanjie, Yanek, Lisa R., Schwander, Karen, Tajuddin, Salman M., Sofer, Tamar, Kim, Wonji, Kayima, James, McKenzie, Colin A., Fox, Ervin, Nalls, Michael A., Young, J. Hunter, Sun, Yan V., Lane, Jacqueline M., Cechova, Sylvia, Zhou, Jie, Tang, Hua, Fornage, Myriam, Musani, Solomon K., Wang, Heming, Lee, Juyoung, Adeyemo, Adebowale, Dreisbach, Albert W., Forrester, Terrence, Chu, Pei-Lun, Cappola, Anne, Evans, Michele K., Morrison, Alanna C., Martin, Lisa W., Wiggins, Kerri L., Hui, Qin, Zhao, Wei, Jackson, Rebecca D., Ware, Erin B., Faul, Jessica D., Reiner, Alex P., Bray, Michael, Denny, Joshua C., Mosley, Thomas H., Palmas, Walter, Guo, Xiuqing, Papanicolaou, George J., Penman, Alan D., Polak, Joseph F., Rice, Kenneth, Taylor, Ken D., Boerwinkle, Eric, Bottinger, Erwin P., Liu, Kiang, Risch, Neil, Hunt, Steven C., Kooperberg, Charles, Zonderman, Alan B., Laurie, Cathy C., Becker, Diane M., Cai, Jianwen, Loos, Ruth J. F., Psaty, Bruce M., Weir, David R., Kardia, Sharon L. R., Arnett, Donna K., Won, Sungho, Edwards, Todd L., Redline, Susan, Cooper, Richard S., Rao, D. C., Rotter, Jerome I., Rotimi, Charles, Levy, Daniel, Chakravarti, Aravinda, Zhu, Xiaofeng, Franceschini, Nora
Publicado no PLoS Genet (2017)