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Demographic and clinical characteristics associated with treatment status in family members with obsessive-compulsive disorder.
Published in:
Depression & Anxiety (1091-4269), 2008, v. 25, n. 3, p. 218, doi. 10.1002/da.20293
By:
- Cullen, Bernadette;
- Samuels, Jack F.;
- Pinto, Anthony;
- Fyer, Abby J.;
- McCracken, James T.;
- Rauch, Scott L.;
- Murphy, Dennis L.;
- Greenberg, Benjamin D.;
- Knowles, James A.;
- Piacentini, John;
- Bienvenu III, O. Joseph;
- Grados, Marco A.;
- Riddle, Mark A.;
- Rasmussen, Steven A.;
- Pauls, David L.;
- Willour, Virginia L.;
- Shugart, Yin Y.;
- Kung-Yee Liang;
- Hoehn-Saric, Rudolf;
- Nestadt, Gerald
Publication type:
Article
Genetic Studies of Usher Syndrome.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 167, doi. 10.1111/j.1749-6632.1991.tb19585.x
By:
- KIMBERLING, W. J.;
- WESTON, M. D.;
- DAHL, S. PIEKE;
- KENYON, J. B.;
- SHUGART, Y. Y.;
- MOLLER, C.;
- DAVENPORT, S. L. H.;
- MARTINI, A.;
- MILANI, M.;
- SMITH, R. J.
Publication type:
Article
The Search for Branchiootorenal Syndrome on Chromosomes 1 and 8.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 288, doi. 10.1111/j.1749-6632.1991.tb19607.x
By:
- COMEAU, K.;
- KIMBERLING, W. J.;
- CREMERS, C. W. R. J.;
- SHUGART, Y.
Publication type:
Article
Report on Attempts to Localize Usher Syndrome Type 1 by Linkage Analysis to Selected Candidate Regions.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 298, doi. 10.1111/j.1749-6632.1991.tb19612.x
By:
- DAHL, S. PIEKE;
- WESTON, M. D.;
- KIMBERLING, W. J.;
- KENYON, J. B.;
- SHUGART, Y. Y.;
- SMITH, R. J. H.
Publication type:
Article
High rate of disease-related copy number variations in childhood onset schizophrenia.
Published in:
Molecular Psychiatry, 2014, v. 19, n. 5, p. 568, doi. 10.1038/mp.2013.59
By:
- Ahn, K;
- Gotay, N;
- Andersen, T M;
- Anvari, A A;
- Gochman, P;
- Lee, Y;
- Sanders, S;
- Guha, S;
- Darvasi, A;
- Glessner, J T;
- Hakonarson, H;
- Lencz, T;
- State, M W;
- Shugart, Y Y;
- Rapoport, J L
Publication type:
Article
Independence of familial transmission of mania and depression: results of the NIMH family study of affective spectrum disorders.
Published in:
Molecular Psychiatry, 2014, v. 19, n. 2, p. 272, doi. 10.1038/mp.2013.181
By:
- Merikangas, K R;
- Cui, L;
- Heaton, L;
- Nakamura, E;
- Roca, C;
- Ding, J;
- Qin, H;
- Guo, W;
- Yao-Shugart, Y;
- Zarate, C;
- Angst, J
Publication type:
Article
Independence of familial transmission of mania and depression: results of the NIMH family study of affective spectrum disorders.
Published in:
Molecular Psychiatry, 2014, v. 19, n. 2, p. 214, doi. 10.1038/mp.2013.116
By:
- Merikangas, K R;
- Cui, L;
- Heaton, L;
- Nakamura, E;
- Roca, C;
- Ding, J;
- Qin, H;
- Guo, W;
- Yao-Shugart, Y;
- Zarate, C;
- Angst, J
Publication type:
Article
Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.
Published in:
Molecular Psychiatry, 2013, v. 18, n. 2, p. 264, doi. 10.1038/mp.2012.45
By:
- Chen, D T;
- Jiang, X;
- Akula, N;
- Shugart, Y Y;
- Wendland, J R;
- Steele, C J M;
- Kassem, L;
- Park, J-H;
- Chatterjee, N;
- Jamain, S;
- Cheng, A;
- Leboyer, M;
- Muglia, P;
- Schulze, T G;
- Cichon, S;
- Nöthen, M M;
- Rietschel, M;
- McMahon, F J
Publication type:
Article
Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.
Published in:
Molecular Psychiatry, 2013, v. 18, n. 2, p. 195, doi. 10.1038/mp.2011.157
By:
- Chen, D T;
- Jiang, X;
- Akula, N;
- Shugart, Y Y;
- Wendland, J R;
- Steele, C J M;
- Kassem, L;
- Park, J-H;
- Chatterjee, N;
- Jamain, S;
- Cheng, A;
- Leboyer, M;
- Muglia, P;
- Schulze, T G;
- Cichon, S;
- Nöthen, M M;
- Rietschel, M;
- McMahon, F J
Publication type:
Article
Association of SLC6A4 variants with obsessive-compulsive disorder in a large multicenter US family study.
Published in:
Molecular Psychiatry, 2011, v. 16, n. 1, p. 108, doi. 10.1038/mp.2009.100
By:
- Voyiaziakis, E.;
- Evgrafov, O.;
- D. Li;
- H-J Yoon;
- Tabares, P.;
- Samuels, J.;
- Y. Wang;
- Riddle, M. A.;
- Grados, M. A.;
- Bienvenu, O. J.;
- Shugart, Y. Y.;
- K-Y Liang;
- Greenberg, B. D.;
- Rasmussen, S. A.;
- Murphy, D. L.;
- Wendland, J. R.;
- McCracken, J. T.;
- Piacentini, J.;
- Rauch, S. L.;
- Pauls, D. L.
Publication type:
Article
Corrigendum: Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome.
Published in:
2004
By:
- Ferland, R. J.;
- Eyaid, W.;
- Collura, R. V.;
- Tully, L. D.;
- Hill, R. S.;
- Al-Nouri, D.;
- Al-Rumayyan, A.;
- Topcu, M.;
- Gascon, G.;
- Bodell, A.;
- Shugart, Y. Y.;
- Ruvolo, M.;
- Walsh, C. A.
Publication type:
Correction Notice
An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29.
Published in:
Genes & Immunity, 2008, v. 9, n. 2, p. 161, doi. 10.1038/sj.gene.6364460
By:
- Shugart, Y. Y.;
- Silverberg, M. S.;
- Duerr, R. H.;
- Taylor, K. D.;
- Wang, M.-H.;
- Zarfas, K.;
- Schumm, L. P.;
- Bromfield, G.;
- Steinhart, A. H.;
- Griffiths, A.M.;
- Kane, S. V.;
- Barmada, M. M.;
- Rotter, J. I.;
- Mei, L.;
- Bernstein, C. N.;
- Bayless, T. M.;
- Langelier, D.;
- Cohen, A.;
- Bitton, A.;
- Rioux, J. D.
Publication type:
Article
Covariate-based linkage analysis: application of a propensity score as the single covariate consistently improves power to detect linkage.
Published in:
European Journal of Human Genetics, 2006, v. 14, n. 9, p. 1018, doi. 10.1038/sj.ejhg.5201650
By:
- Doan, Betty Q;
- Sorant, Alexa J M;
- Frangakis, Constantine E;
- Bailey-Wilson, Joan E;
- Shugart, Yin Y
Publication type:
Article
Multipoint genomic scanning for quantitative loci: effects of map density, sibship size and computational approach.
Published in:
European Journal of Human Genetics, 1999, v. 7, n. 2, p. 103, doi. 10.1038/sj.ejhg.5200280
By:
- Shugart, Yin Y;
- Goldgar, David E
Publication type:
Article
The early growth response protein 1-miR-30a-5p-neurogenic differentiation factor 1 axis as a novel biomarker for schizophrenia diagnosis and treatment monitoring.
Published in:
Translational Psychiatry, 2017, v. 7, n. 1, p. e998, doi. 10.1038/tp.2016.268
By:
- Liu, S;
- Zhang, F;
- Shugart, Y Y;
- Yang, L;
- Li, X;
- Liu, Z;
- Sun, N;
- Yang, C;
- Guo, X;
- Shi, J;
- Wang, L;
- Cheng, L;
- Zhang, K;
- Yang, T;
- Xu, Y
Publication type:
Article
Family-based tests applied to extended pedigrees identify rare variants related to hypertension.
Published in:
BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S31
By:
- Mengyuan Xu;
- Wang, Harold Z.;
- Wei Guo;
- Haide Qin;
- Shugart, Yin Y.
Publication type:
Article
Rare plus common SERT variants in obsessive-compulsive disorder.
Published in:
2007
By:
- Grados, M. A.;
- Samuels, J.;
- Shugart, Y. Y.;
- Willour, V. L.;
- Wang, Y.;
- Cullen, B.;
- Bienvenu, O .J.;
- Hoehn-Saric, R.;
- Valle, D.;
- Liang, K.-Y.;
- Riddle, M. A.;
- Wendland, J.R.;
- Murphy, D. L.;
- Nestadt, G.;
- Detera-Wadleigh, S.
Publication type:
Letter
Genomewide linkage scan for obsessive-compulsive disorder: evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q.
Published in:
Molecular Psychiatry, 2006, v. 11, n. 8, p. 763, doi. 10.1038/sj.mp.4001847
By:
- Shugart, Y. Y.;
- Samuels, J.;
- Willour, V. L.;
- Grados, M. A.;
- Greenberg, B. D.;
- Knowles, J. A.;
- McCracken, J. T.;
- Rauch, S. L.;
- Murphy, D. L.;
- Wang, Y.;
- Pinto, A.;
- Fyer, A. J.;
- Piacentini, J.;
- Pauls, D. L.;
- Cullen, B.;
- Page, J.;
- Rasmussen, S. A.;
- Bienvenu, O. J.;
- Hoehn-Saric, R.;
- Valle, D.
Publication type:
Article
CGH-targeted linkage analysis reveals a possible BRCA1 modifier locus on chromosome 5q.
Published in:
Human Molecular Genetics, 2002, v. 11, n. 11, p. 1327, doi. 10.1093/hmg/11.11.1327
By:
- Nathanson, Katherine L.;
- Shugart, Yin Y.;
- Omaruddin, Romaica;
- Szabo, Csilla;
- Goldgar, David;
- Rebbeck, Timothy R.;
- Weber, Barbara L.
Publication type:
Article
Comparison of Sib Pair-Based Approaches for Identifying Quantitative Trait Loci Underlying Asthma in the Busselton Families.
Published in:
Genetic Epidemiology, 2001, v. 21, p. S198, doi. 10.1002/gepi.2001.21.s1.s198
By:
- Shugart, Yin Y.;
- Specchia, Claudia;
- Li, Hui-Hua;
- Doan, Betty Q.;
- Mathias, Rasika A.;
- Devoto, Marcella
Publication type:
Article
The impact of redefining affection status for alcoholism on affected-sib-pair analysis.
Published in:
Genetic Epidemiology, 1999, v. 17, p. S151, doi. 10.1002/gepi.1370170726
By:
- Fann, Cathy S.J.;
- Shugart, Yin Y.;
- Lachman, Herb;
- Collins, Andrew;
- Chang, C.J.
Publication type:
Article
The performance of MIM in comparison with MAPMAKER/SIBS to detect QTLs.
Published in:
Genetic Epidemiology, 1997, v. 14, n. 6, p. 897, doi. 10.1002/(SICI)1098-2272(1997)14:6<897::AID-GEPI56>3.0.CO;2-H
By:
- Shugart, Yin Y.;
- Goldgar, David E.
Publication type:
Article
Precision of marker heterozygosity estimates.
Published in:
Genetic Epidemiology, 1995, v. 12, n. 6, p. 671, doi. 10.1002/gepi.1370120625
By:
- Shugart, Yin Y.
Publication type:
Article
Segregation analysis of autosomal dominant polycystic kidney disease.
Published in:
Genetic Epidemiology, 1993, v. 10, n. 3, p. 189, doi. 10.1002/gepi.1370100305
By:
- Dobin, A.;
- Kimberling, W. J.;
- Pettinger, W.;
- Bailey-Wilson, J. E.;
- Shugart, Y. Y.;
- Gabow, P.
Publication type:
Article
A Novel Mixture Model to Estimate the Time to Drug Effect Onset and Its Association with Covariates.
Published in:
Human Heredity, 2016, v. 80, n. 2, p. 90, doi. 10.1159/000440880
By:
- Xu, Meng Yuan;
- Umbach, David M.;
- Murphy, Eleanor;
- McMahon, Francis;
- Shugart, Yin Y.
Publication type:
Article

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