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The best of times, the worst of times for psychiatric disease.
Published in:
Nature Neuroscience, 2012, v. 15, n. 6, p. 811, doi. 10.1038/nn.3115
By:
- Karayiorgou, Maria;
- Flint, Jonathan;
- Gogos, Joseph A;
- Malenka, Robert C;
- Bargmann, Cornelia I;
- Boyden, Edward S;
- Bullmore, Edward T;
- Chan, Anthony W;
- Davis, Michael;
- Deisseroth, Karl;
- Dolmetch, Ricardo E;
- Eggan, Kevin;
- Fears, Scott C;
- Freimer, Nelson B;
- Geschwind, Daniel H;
- Gordon, Joshua;
- Nickerson, Debbie A;
- Vanderhaeghen, Pierre;
- Axel, Richard;
- Zuker, Charles S
Publication type:
Article
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.
Published in:
PLoS Genetics, 2016, v. 12, n. 4, p. 1, doi. 10.1371/journal.pgen.1005963
By:
- Priest, James R.;
- Osoegawa, Kazutoyo;
- Mohammed, Nebil;
- Nanda, Vivek;
- Kundu, Ramendra;
- Schultz, Kathleen;
- Lammer, Edward J.;
- Girirajan, Santhosh;
- Scheetz, Todd;
- Waggott, Daryl;
- Haddad, Francois;
- Reddy, Sushma;
- Bernstein, Daniel;
- Burns, Trudy;
- Steimle, Jeffrey D.;
- Yang, Xinan H.;
- Moskowitz, Ivan P.;
- Hurles, Matthew;
- Lifton, Richard P.;
- Nickerson, Debbie
Publication type:
Article
Correction: Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis.
Published in:
2015
By:
- Emond, Mary J.;
- Louie, Tin;
- Emerson, Julia;
- Chong, Jessica X.;
- Mathias, Rasika A.;
- Knowles, Michael R.;
- Rieder, Mark J.;
- Tabor, Holly K.;
- Nickerson, Debbie A.;
- Barnes, Kathleen C.;
- null, null;
- GO, Lung;
- Gibson, Ronald L.;
- Bamshad, Michael J.
Publication type:
Correction Notice
Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis.
Published in:
PLoS Genetics, 2015, v. 11, n. 6, p. 1, doi. 10.1371/journal.pgen.1005273
By:
- Emond, Mary J.;
- Louie, Tin;
- Emerson, Julia;
- Chong, Jessica X.;
- Mathias, Rasika A.;
- Knowles, Michael R.;
- Rieder, Mark J.;
- Tabor, Holly K.;
- Nickerson, Debbie A.;
- Barnes, Kathleen C.;
- null, null;
- GO, Lung;
- Gibson, Ronald L.;
- Bamshad, Michael J.
Publication type:
Article
Genome-Wide Association Study Identifies Genetic Loci Associated with Iron Deficiency.
Published in:
PLoS ONE, 2011, v. 6, n. 3, p. 1, doi. 10.1371/journal.pone.0017390
By:
- McLaren, Christine E.;
- Garner, Chad P.;
- Constantine, Clare C.;
- McLachlan, Stela;
- Vulpe, Chris D.;
- Snively, Beverly M.;
- Gordeuk, Victor R.;
- Nickerson, Debbie A.;
- Cook, James D.;
- Leiendecker-Foster, Catherine;
- Beckman, Kenneth B.;
- Eckfeldt, John H.;
- Barcellos, Lisa F.;
- Murray, Joseph A.;
- Adams, Paul C.;
- Acton, Ronald T.;
- Killeen, Anthony A.;
- McLaren, Gordon D.
Publication type:
Article
Detection of structural variants and indels within exome data.
Published in:
Nature Methods, 2012, v. 9, n. 2, p. 176, doi. 10.1038/nmeth.1810
By:
- Karakoc, Emre;
- Alkan, Can;
- O'Roak, Brian J;
- Dennis, Megan Y;
- Vives, Laura;
- Mark, Kenneth;
- Rieder, Mark J;
- Nickerson, Debbie A;
- Eichler, Evan E
Publication type:
Article
Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene.
Published in:
Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-018-0343-z
By:
- Patowary, Ashok;
- Won, So Yeon;
- Oh, Shin Ji;
- Nesbitt, Ryan R;
- Archer, Marilyn;
- Nickerson, Debbie;
- Raskind, Wendy H.;
- Bernier, Raphael;
- Lee, Ji Eun;
- Brkanac, Zoran
Publication type:
Article
De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders.
Published in:
PLoS Genetics, 2018, v. 14, n. 12, p. 1, doi. 10.1371/journal.pgen.1007822
By:
- Guo, Yicheng;
- Qi, Hongjian;
- Zhou, Xueya;
- Zhu, Na;
- Zhao, Haoquan;
- Kitaygorodsky, Alexander;
- Shen, Yufeng;
- Warner, Brad W.;
- Mychaliska, George B.;
- Potoka, Douglas;
- Wagner, Amy J.;
- ElFiky, Mahmoud;
- Wilson, Jay M.;
- High, Frances A.;
- Longoni, Mauro;
- Donahoe, Patricia K.;
- Nickerson, Debbie;
- Bamshad, Michael;
- Yu, Lan;
- Wynn, Julia
Publication type:
Article
FOXE3 mutations predispose to thoracic aortic aneurysms and dissections.
Published in:
2016
By:
- Shao-Qing Kuang;
- Medina-Martinez, Olga;
- Dong-chuan Guo;
- Limin Gong;
- Regalado, Ellen S.;
- Reynolds, Corey L.;
- Boileau, Catherine;
- Jondeau, Guillaume;
- Prakash, Siddharth K.;
- Kwartler, Callie S.;
- Yang Zhu, Lawrence;
- Peters, Andrew M.;
- Xue-Yan Duan;
- Bamshad, Michael J.;
- Shendure, Jay;
- Nickerson, Debbie A.;
- Santos-Cortez, Regie L.;
- Xiurong Dong;
- Lea, Suzanne M.;
- Majesky, Mark W.
Publication type:
journal article
Inferring Clonal Composition from Multiple Sections of a Breast Cancer.
Published in:
PLoS Computational Biology, 2014, v. 10, n. 7, p. 1, doi. 10.1371/journal.pcbi.1003703
By:
- Zare, Habil;
- Wang, Junfeng;
- Hu, Alex;
- Weber, Kris;
- Smith, Josh;
- Nickerson, Debbie;
- Song, ChaoZhong;
- Witten, Daniela;
- Blau, C. Anthony;
- Noble, William Stafford
Publication type:
Article

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