المؤلفون: Gillis Tammy, Mysore Jayalakshmi, Djoussé Luc, Xu Gang, Prakash Ranjana, Wheeler Vanessa C, Lazzarini Alice, Ashizawa Tetsuo, Jones Randi, Paulsen Jane S, Frontali Marina, Novelletto Andrea, McCusker Elizabeth, Trent Ronald JA, Klimek Mary, Suchowersky Oksana, García Carmen, Gómez-Tortosa Estrella, Frati Luigi, Squitieri Ferdinando, Rosenblatt Adam, Margolis Russell L, Ross Christopher A, Nance Martha, Morrison Patrick J, Durr Alexandra, Warby Simon C, Hayden Michael R, Li Jian-Liang, Hakky Michael, Cupples L Adrienne, Saint-Hilaire Marie H, Cha Jang-Ho J, Hersch Steven M, Penney John B, Harrison Madaline B, Perlman Susan L, Zanko Andrea, Abramson Ruth K, Lechich Anthony J, Duckett Ayana, Marder Karen, Conneally P Michael, Gusella James F, MacDonald Marcy E, Myers Richard H

المصدر: BMC Medical Genetics, Vol 7, Iss 1, p 71 (2006)

مصطلحات موضوعية: Internal medicine, RC31-1245, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://www.biomedcentral.com/1471-2350/7/71; https://doaj.org/toc/1471-2350

URL الوصول: https://doaj.org/article/e3f085610415408f8f263d3a98bea8fe

المؤلفون: Lacourse, Karine, Yetton, Ben, Mednick, Sara, Warby, Simon C

المصدر: Scientific data. 7(1)

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/0xw6w1wg

المؤلفون: Chen, Han, Cade, Brian E, Gleason, Kevin J, Bjonnes, Andrew C, Stilp, Adrienne M, Sofer, Tamar, Conomos, Matthew P, Ancoli-Israel, Sonia, Arens, Raanan, Azarbarzin, Ali, Bell, Graeme I, Below, Jennifer E, Chun, Sung, Evans, Daniel S, Ewert, Ralf, Frazier-Wood, Alexis C, Gharib, Sina A, Haba-Rubio, José, Hagen, Erika W, Heinzer, Raphael, Hillman, David R, Johnson, W Craig, Kutalik, Zoltan, Lane, Jacqueline M, Larkin, Emma K, Lee, Seung Ku, Liang, Jingjing, Loredo, Jose S, Mukherjee, Sutapa, Palmer, Lyle J, Papanicolaou, George J, Penzel, Thomas, Peppard, Paul E, Post, Wendy S, Ramos, Alberto R, Rice, Ken, Rotter, Jerome I, Sands, Scott A, Shah, Neomi A, Shin, Chol, Stone, Katie L, Stubbe, Beate, Sul, Jae Hoon, Tafti, Mehdi, Taylor, Kent D, Teumer, Alexander, Thornton, Timothy A, Tranah, Gregory J, Wang, Chaolong, Wang, Heming, Warby, Simon C, Wellman, D Andrew, Zee, Phyllis C, Hanis, Craig L, Laurie, Cathy C, Gottlieb, Daniel J, Patel, Sanjay R, Zhu, Xiaofeng, Sunyaev, Shamil R, Saxena, Richa, Lin, Xihong, Redline, Susan

المصدر: American Journal of Respiratory Cell and Molecular Biology. 58(3)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Cardiovascular Medicine and Haematology, Genetics, Sleep Research, Clinical Research, Human Genome, Lung, 2.1 Biological and endogenous factors, Aetiology, Adult, Aged, Female, Genome-Wide Association Study, Humans, Male, Middle Aged, Phosphatidylethanolamine N-Methyltransferase, Quantitative Trait Loci, Sex Characteristics, Sleep Apnea, Obstructive, Sleep, REM, Sterol Regulatory Element Binding Protein 1, Trans-Activators, Transcription Factors, ras Proteins, obstructive sleep apnea, genetics, genome-wide association studies, multiethnic, sexual dimorphism, Cardiorespiratory Medicine and Haematology, Respiratory System, Biochemistry and cell biology, Cardiovascular medicine and haematology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/0g88978z

المؤلفون: Wendt, Sabrina L., Welinder, Peter, Sorensen, Helge B.D., Peppard, Paul E., Jennum, Poul, Perona, Pietro, Mignot, Emmanuel, Warby, Simon C.

المصدر: In Clinical Neurophysiology August 2015 126(8):1548-1556

المؤلفون: Chapman, Christine Elaine^Aff4, Macefield, Vaughan G^{Aff5, Aff6}, Essick, Greg K.^Aff7, Trulsson, Mats^Aff8, Iwamura, Yoshiaki^Aff9, Nossaman, Bobby D.^{Aff10, Aff12}, Murthy, Subramanyam N.^Aff10, Gur, Serap^Aff11, Hellstrom, Wayne G., Kadowitz, Philip J.^Aff10, Di Lorenzo, Patricia M.^Aff13, Chen, Jen-Yung^Aff13, Rosen, Andrew M.^Aff13, Roussin, Andre T.^Aff13, Montmayeur, Jean-Pierre^Aff14, Sugita, Makoto^Aff15, Buonviso, Nathalie^Aff16, Cenier, Tristan^Aff16, David, François^Aff16, Carlson, Bruce A.^Aff17, Sandercock, Thomas G.^Aff18, Banes, Albert J.^Aff19, Herzog, Walter^Aff20, Wall, Michelle^Aff21, Tanaka, Hirokazu^Aff22, Kawato, Mitsuo^Aff22, Colwill, Ruth M.^Aff23, Röska-Hardy, Louise^Aff24, Christie, MacDonald J.^Aff25, Gebber, Gerard L.^Aff26, Ehret, Günter^Aff27, Ljubisavljevic, Milos^Aff28, Saito, Tetsuichiro^Aff29, Breer, Heinz^Aff30, Strotmann, Jörg^Aff30, Ohta, Masayoshi^{Aff31, Aff34, Aff35, Aff34, Aff35}, Suzuki, Yoshihisa^{Aff32, Aff34, Aff35, Aff34, Aff35}, Ide, Chizuka^{Aff33, Aff34, Aff36, Aff34, Aff36}, Okano, Hideyuki^Aff37, Plant, Giles W^{Aff38, Aff39}, Xu, Xiao-Ming^Aff40, Vlodavsky, Eugene^Aff41, Warby, Simon C.^Aff42, Semaka, Alicia^Aff42, Hayden, Michael R.^Aff42, Harteneck, Christian^Aff43, Roenneberg, Till^Aff44, Merrow, Martha^Aff45

المساهمون: Binder, Marc D., editor^Aff1, Hirokawa, Nobutaka, editor^Aff2, Windhorst, Uwe, editor^Aff3

المصدر: Encyclopedia of Neuroscience. :3989-4150

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المؤلفون: Fournier, Simon, Dauvilliers, Yves, Warby, Simon C., Labrecque, Marjorie, Zadra, Antonio, Boucetta, Soufiane, El Gewely, Maryam, Kaddioui, Houda, Lopez, Régis, Montplaisir, Jacques Y., Bareke, Eric, Tétreault, Martine, Desautels, Alex

المصدر: Journal of Sleep Research; Aug2022, Vol. 31 Issue 4, p1-8, 8p

مصطلحات موضوعية: ADENOSINE deaminase, SLEEPWALKING, ADENOSINES, MISSENSE mutation, EYE movements, NUCLEOTIDE sequencing

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المؤلفون: Warby, Simon C, Semaka, Alicia, Hayden, Michael R

المصدر: Encyclopedia of Neuroscience. 2009, v. 5, p4131-4136.

مصطلحات موضوعية: Genetic disorders, Trinucleotide repeats, Gene mutation

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