Yin Yao Shugart

Yin Yao Shugart

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Yin Yao Shugart

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Genome-Wide Association Study of Susceptibility Loci for Radiation-Induced Brain Injury.

J Natl Cancer Inst 2018 Oct 8. Epub 2018 Oct 8.

State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Sun Yat-sen University Cancer Center, Guangzhou, China.

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https://academic.oup.com/jnci/advance-article/doi/10.1093/jn
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http://dx.doi.org/10.1093/jnci/djy150DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6579742PMC
October 2018

Nuclear Norm Clustering: a promising alternative method for clustering tasks.

Sci Rep 2018 Jul 18;8(1):10873. Epub 2018 Jul 18.

State Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai, China.

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http://www.nature.com/articles/s41598-018-29246-4
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http://dx.doi.org/10.1038/s41598-018-29246-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052164PMC
July 2018

Diagnostic value of blood-derived microRNAs for schizophrenia: results of a meta-analysis and validation.

Sci Rep 2017 11 10;7(1):15328. Epub 2017 Nov 10.

Department of Psychiatry, First Hospital/First Clinical Medical College of Shanxi Medical University, Taiyuan, 030001, P. R. China.

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http://dx.doi.org/10.1038/s41598-017-15751-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681644PMC
November 2017

Bagging Nearest-Neighbor Prediction independence Test: an efficient method for nonlinear dependence of two continuous variables.

Sci Rep 2017 10 6;7(1):12736. Epub 2017 Oct 6.

State Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai, China.

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http://dx.doi.org/10.1038/s41598-017-12783-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630623PMC
October 2017

Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia.

J Genet Genomics 2017 Jun 8;44(6):295-306. Epub 2017 Jun 8.

Institute of Mental Health, National Clinical Research Center for Mental Health Disorders and National Technology Institute of Psychiatry, and Key Laboratory of Psychiatry and Mental Health of Hunan Province, The Second Xiangya Hospital, Central South University, Changsha 410011, China. Electronic address:

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http://dx.doi.org/10.1016/j.jgg.2017.05.005DOI Listing
June 2017

ADAR2 functions as a tumor suppressor via editing IGFBP7 in esophageal squamous cell carcinoma.

Int J Oncol 2017 Feb 29;50(2):622-630. Epub 2016 Dec 29.

State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong 510060, P.R. China.

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http://dx.doi.org/10.3892/ijo.2016.3823DOI Listing
February 2017

Integrating multiple genomic data: sparse representation based biomarker selection for blood pressure.

BMC Proc 2016 18;10(Suppl 7):283-288. Epub 2016 Oct 18.

Unit on Statistical Genomics, Division of Intramural Research Programs, National Institute of Mental Health, National Institutes of Health, Building 35, Room 3A 1000, 35 Convent Drive, Bethesda, MD 20892 USA.

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http://dx.doi.org/10.1186/s12919-016-0044-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133507PMC
October 2016

Random Bits Forest: a Strong Classifier/Regressor for Big Data.

Sci Rep 2016 07 22;6:30086. Epub 2016 Jul 22.

Ministry of Education Key Laboratory of Contemporary Anthropology, Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai 200433, China.

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http://dx.doi.org/10.1038/srep30086DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957112PMC
July 2016

No association between ZNF804A rs1344706 and schizophrenia in a case-control study of Han Chinese.

Neurosci Lett 2016 Apr 2;618:14-18. Epub 2016 Mar 2.

Wuxi Mental Health Center of Nanjing Medical University, Wuxi, Jiangsu 214151, China. Electronic address:

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http://dx.doi.org/10.1016/j.neulet.2016.02.048DOI Listing
April 2016

Mapsnp: an R package to plot a genomic map for single nucleotide polymorphisms.

PLoS One 2015 8;10(4):e0123609. Epub 2015 Apr 8.

Unit on Statistical Genomics, Intramural Research Program, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0123609PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390227PMC
March 2016

Three dysconnectivity patterns in treatment-resistant schizophrenia patients and their unaffected siblings.

Neuroimage Clin 2015 24;8:95-103. Epub 2015 Mar 24.

Institute of Mental Health, The Second Xiangya Hospital of Central South University, 139 Renmin Road, Changsha, Hunan 410011, China ; State Key Laboratory of Medical Genetics, Central South University, Changsha, Hunan 410078, China ; National Technology of Institute of Psychiatry, Central South University, Changsha, Hunan 410011, China.

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http://dx.doi.org/10.1016/j.nicl.2015.03.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4473730PMC
March 2016

Potential involvement of the interleukin-18 pathway in schizophrenia.

J Psychiatr Res 2016 Mar 15;74:10-6. Epub 2015 Dec 15.

Institute of Mental Health, Sixth Hospital, Peking University, Beijing, China; Key Laboratory of Mental Health, Ministry of Health & National Clinical Research Center for Mental Disorders (Peking University), Beijing, China; Peking-Tsinghua Center for Life Sciences/PKU-IDG/McGovern Institute for Brain Research, Peking University, Beijing, China.

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http://dx.doi.org/10.1016/j.jpsychires.2015.12.013DOI Listing
March 2016

Evidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders.

BMC Genomics 2016 Mar 1;17:163. Epub 2016 Mar 1.

Unit on Statistical Genomics, Intramural Research Program, National Institute of Mental Health, National Institute of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1186/s12864-016-2475-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774106PMC
March 2016

Altered expression of mRNA profiles in blood of early-onset schizophrenia.

Sci Rep 2016 Jan 6;6:16767. Epub 2016 Jan 6.

Institute of Mental Health, Sixth Hospital, Peking University; Beijing 100191, China.

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http://dx.doi.org/10.1038/srep16767DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702094PMC
January 2016

Increased Variability of Genomic Transcription in Schizophrenia.

Sci Rep 2015 Dec 10;5:17995. Epub 2015 Dec 10.

Department of Psychiatry, First Hospital /First Clinical Medical College of Shanxi Medical University, Taiyuan, China.

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http://dx.doi.org/10.1038/srep17995DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675071PMC
December 2015

Further evidence supporting the association of NKAPL with schizophrenia.

Neurosci Lett 2015 Sep 18;605:49-52. Epub 2015 Aug 18.

Wuxi Mental Health Center of Nanjing Medical University, Wuxi, Jiangsu, China. Electronic address:

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http://dx.doi.org/10.1016/j.neulet.2015.08.023DOI Listing
September 2015

New findings support the association of DISC1 genetic variants with susceptibility to schizophrenia in the Han Chinese population.

Psychiatry Res 2015 Aug 28;228(3):966-8. Epub 2015 Jun 28.

Divsion ofIntramuralResearchProgram, National InstituteofMentalHealth,NationalInstitutesofHealth, Building 35,Room3A1000,35ConventDrive, Bethesda, MD20892,USA.

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http://dx.doi.org/10.1016/j.psychres.2015.05.115DOI Listing
August 2015

Efficient test for nonlinear dependence of two continuous variables.

BMC Bioinformatics 2015 Aug 19;16:260. Epub 2015 Aug 19.

Ministry of Education Key Laboratory of Contemporary Anthropology, Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University, Shanghai, 200433, China.

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http://bmcbioinformatics.biomedcentral.com/articles/10.1186/
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http://dx.doi.org/10.1186/s12859-015-0697-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539721PMC
August 2015

Heterogeneity revealed through meta-analysis might link geographical differences with nasopharyngeal carcinoma incidence in Han Chinese populations.

BMC Cancer 2015 Aug 26;15:598. Epub 2015 Aug 26.

Division of Intramural Research Programs, Unit on Statistical Genomics, National Institute of Mental Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1186/s12885-015-1607-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4549009PMC
August 2015

Converging evidence implicates the abnormal microRNA system in schizophrenia.

Schizophr Bull 2015 May 26;41(3):728-35. Epub 2014 Nov 26.

Department of Psychiatry, The Sixth Affiliated Hospital and Institute for Mental Health of Peking University/Key Laboratory of Mental Health, Ministry of Health, Beijing, China; Peking-Tsinghua Center for Life Sciences/PKU-IDG/McGovern Institute for Brain Research, Peking University, Beijing, China

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http://dx.doi.org/10.1093/schbul/sbu148DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393688PMC
May 2015

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

Authors:
Dongmei Yu Carol A Mathews Jeremiah M Scharf Benjamin M Neale Lea K Davis Eric R Gamazon Eske M Derks Patrick Evans Christopher K Edlund Jacquelyn Crane Jesen A Fagerness Lisa Osiecki Patience Gallagher Gloria Gerber Stephen Haddad Cornelia Illmann Lauren M McGrath Catherine Mayerfeld Sampath Arepalli Cristina Barlassina Cathy L Barr Laura Bellodi Fortu Benarroch Gabriel Bedoya Berrió O Joseph Bienvenu Donald W Black Michael H Bloch Helena Brentani Ruth D Bruun Cathy L Budman Beatriz Camarena Desmond D Campbell Carolina Cappi Julio C Cardona Silgado Maria C Cavallini Denise A Chavira Sylvain Chouinard Edwin H Cook M R Cookson Vladimir Coric Bernadette Cullen Daniele Cusi Richard Delorme Damiaan Denys Yves Dion Valsama Eapen Karin Egberts Peter Falkai Thomas Fernandez Eduardo Fournier Helena Garrido Daniel Geller Donald L Gilbert Simon L Girard Hans J Grabe Marco A Grados Benjamin D Greenberg Varda Gross-Tsur Edna Grünblatt John Hardy Gary A Heiman Sian M J Hemmings Luis D Herrera Dianne M Hezel Pieter J Hoekstra Joseph Jankovic James L Kennedy Robert A King Anuar I Konkashbaev Barbara Kremeyer Roger Kurlan Nuria Lanzagorta Marion Leboyer James F Leckman Leonhard Lennertz Chunyu Liu Christine Lochner Thomas L Lowe Sara Lupoli Fabio Macciardi Wolfgang Maier Paolo Manunta Maurizio Marconi James T McCracken Sandra C Mesa Restrepo Rainald Moessner Priya Moorjani Jubel Morgan Heike Muller Dennis L Murphy Allan L Naarden Erika Nurmi William Cornejo Ochoa Roel A Ophoff Andrew J Pakstis Michele T Pato Carlos N Pato John Piacentini Christopher Pittenger Yehuda Pollak Scott L Rauch Tobias Renner Victor I Reus Margaret A Richter Mark A Riddle Mary M Robertson Roxana Romero Maria C Rosário David Rosenberg Stephan Ruhrmann Chiara Sabatti Erika Salvi Aline S Sampaio Jack Samuels Paul Sandor Susan K Service Brooke Sheppard Harvey S Singer Jan H Smit Dan J Stein Eric Strengman Jay A Tischfield Maurizio Turiel Ana V Valencia Duarte Homero Vallada Jeremy Veenstra-VanderWeele Susanne Walitza Ying Wang Mike Weale Robert Weiss Jens R Wendland Herman G M Westenberg Yin Yao Shugart Ana G Hounie Euripedes C Miguel Humberto Nicolini Michael Wagner Andres Ruiz-Linares Danielle C Cath William McMahon Danielle Posthuma Ben A Oostra Gerald Nestadt Guy A Rouleau Shaun Purcell Michael A Jenike Peter Heutink Gregory L Hanna David V Conti Paul D Arnold Nelson B Freimer S Evelyn Stewart James A Knowles Nancy J Cox David L Pauls

Am J Psychiatry 2015 Jan 31;172(1):82-93. Epub 2014 Oct 31.

From the Psychiatric and Neurodevelopmental Genetics Unit, Center for Human Genetics Research, Department of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Boston; the Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT, Cambridge, Mass.; the Department of Psychiatry, University of California, San Francisco; the Department of Neurology, Massachusetts General Hospital, Boston; the Division of Cognitive and Behavioral Neurology, Brigham and Women's Hospital, Boston; the Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston; Section of Genetic Medicine, Department of Medicine, University of Chicago, Chicago; the Department of Psychiatry, Academic Medical Center, University of Amsterdam, Amsterdam; the Department of Preventive Medicine, Division of Biostatistics, Keck School of Medicine, University of Southern California, Los Angeles; the Laboratory of Neurogenetics, National Institute on Aging, Bethesda, Md.; the Genomic and Bioinformatic Unit, Filarete Foundation, Milan, Italy; the Department of Health Sciences, Graduate School of Nephrology, University of Milan, Milan; the Toronto Western Research Institute, University Health Network, Toronto; Hospital for Sick Children, Toronto; Università Vita-Salute San Raffaele, Milan; the Herman Dana Division of Child and Adolescent Psychiatry, Hadassah-Hebrew University Medical Center, Jerusalem; Universidad de Antioquia, Universidad Pontificia Bolivariana, Medellín, Colombia; the Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore; the Department of Psychiatry, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City; the Child Study Center and the Department of Psychiatry, Yale University School of Medicine, New Haven, Conn.; the Department of Psychiatry, University of São Paulo Medical School, São Paulo, Brazil; North Shore-Long Island Jewish Medical Center and North Shore-Lo

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http://dx.doi.org/10.1176/appi.ajp.2014.13101306DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282594PMC
January 2015

Sparse representation based biomarker selection for schizophrenia with integrated analysis of fMRI and SNPs.

Neuroimage 2014 Nov 12;102 Pt 1:220-8. Epub 2014 Feb 12.

Department of Biomedical Engineering, Tulane University, New Orleans, LA, USA; Department of Biostatistics & Bioinformatics, Tulane University, New Orleans, LA, USA. Electronic address:

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http://ieeexplore.ieee.org/iel7/6548349/6556393/06556585.pdf
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http://linkinghub.elsevier.com/retrieve/pii/S105381191400042
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http://dx.doi.org/10.1016/j.neuroimage.2014.01.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4130811PMC
November 2014

How genome-wide SNP-SNP interactions relate to nasopharyngeal carcinoma susceptibility.

PLoS One 2013 23;8(12):e83034. Epub 2013 Dec 23.

Chang Gung Molecular Medicine Research Center, Chang Gung University, Taoyuan, Taiwan.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0083034PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871583PMC
October 2014

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.

Authors:
Lauren M McGrath Dongmei Yu Christian Marshall Lea K Davis Bhooma Thiruvahindrapuram Bingbin Li Carolina Cappi Gloria Gerber Aaron Wolf Frederick A Schroeder Lisa Osiecki Colm O'Dushlaine Andrew Kirby Cornelia Illmann Stephen Haddad Patience Gallagher Jesen A Fagerness Cathy L Barr Laura Bellodi Fortu Benarroch O Joseph Bienvenu Donald W Black Michael H Bloch Ruth D Bruun Cathy L Budman Beatriz Camarena Danielle C Cath Maria C Cavallini Sylvain Chouinard Vladimir Coric Bernadette Cullen Richard Delorme Damiaan Denys Eske M Derks Yves Dion Maria C Rosário Valsama Eapen Patrick Evans Peter Falkai Thomas V Fernandez Helena Garrido Daniel Geller Hans J Grabe Marco A Grados Benjamin D Greenberg Varda Gross-Tsur Edna Grünblatt Gary A Heiman Sian M J Hemmings Luis D Herrera Ana G Hounie Joseph Jankovic James L Kennedy Robert A King Roger Kurlan Nuria Lanzagorta Marion Leboyer James F Leckman Leonhard Lennertz Christine Lochner Thomas L Lowe Gholson J Lyon Fabio Macciardi Wolfgang Maier James T McCracken William McMahon Dennis L Murphy Allan L Naarden Benjamin M Neale Erika Nurmi Andrew J Pakstis Michele T Pato Carlos N Pato John Piacentini Christopher Pittenger Yehuda Pollak Victor I Reus Margaret A Richter Mark Riddle Mary M Robertson David Rosenberg Guy A Rouleau Stephan Ruhrmann Aline S Sampaio Jack Samuels Paul Sandor Brooke Sheppard Harvey S Singer Jan H Smit Dan J Stein Jay A Tischfield Homero Vallada Jeremy Veenstra-VanderWeele Susanne Walitza Ying Wang Jens R Wendland Yin Yao Shugart Euripedes C Miguel Humberto Nicolini Ben A Oostra Rainald Moessner Michael Wagner Andres Ruiz-Linares Peter Heutink Gerald Nestadt Nelson Freimer Tracey Petryshen Danielle Posthuma Michael A Jenike Nancy J Cox Gregory L Hanna Helena Brentani Stephen W Scherer Paul D Arnold S Evelyn Stewart Carol A Mathews James A Knowles Edwin H Cook David L Pauls Kai Wang Jeremiah M Scharf

J Am Acad Child Adolesc Psychiatry 2014 Aug 24;53(8):910-9. Epub 2014 Jun 24.

Massachusetts General Hospital, Boston; Brigham and Womens Hospital, Boston; Harvard-MIT Broad Institute, Boston. Electronic address:

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http://dx.doi.org/10.1016/j.jaac.2014.04.022DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4218748PMC
August 2014

The power comparison of the haplotype-based collapsing tests and the variant-based collapsing tests for detecting rare variants in pedigrees.

BMC Genomics 2014 Jul 28;15:632. Epub 2014 Jul 28.

Division of Intramural Division Program, National Institute of Mental Health, National Institute of Health, 35 Convent Drive, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1186/1471-2164-15-632DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131059PMC
July 2014

Association analysis of a functional variant in ATXN2 with schizophrenia.

Neurosci Lett 2014 Mar 9;562:24-7. Epub 2013 Dec 9.

Institute of Mental Health, Peking University, Beijing, China; Key Laboratory of Mental Health, Ministry of Health, Beijing, China. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S03043940130107
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http://dx.doi.org/10.1016/j.neulet.2013.12.001DOI Listing
March 2014

New insights into the genetic mechanism of IQ in autism spectrum disorders.

Front Genet 2013 18;4:195. Epub 2013 Oct 18.

Unit on Statistical Genomics, Intramural Research Program, National Institute of Mental Health, National Institutes of Health Bethesda, MD, USA.

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http://dx.doi.org/10.3389/fgene.2013.00195DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799005PMC
October 2013

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.

Authors:
Lea K Davis Dongmei Yu Clare L Keenan Eric R Gamazon Anuar I Konkashbaev Eske M Derks Benjamin M Neale Jian Yang S Hong Lee Patrick Evans Cathy L Barr Laura Bellodi Fortu Benarroch Gabriel Bedoya Berrio Oscar J Bienvenu Michael H Bloch Rianne M Blom Ruth D Bruun Cathy L Budman Beatriz Camarena Desmond Campbell Carolina Cappi Julio C Cardona Silgado Danielle C Cath Maria C Cavallini Denise A Chavira Sylvain Chouinard David V Conti Edwin H Cook Vladimir Coric Bernadette A Cullen Dieter Deforce Richard Delorme Yves Dion Christopher K Edlund Karin Egberts Peter Falkai Thomas V Fernandez Patience J Gallagher Helena Garrido Daniel Geller Simon L Girard Hans J Grabe Marco A Grados Benjamin D Greenberg Varda Gross-Tsur Stephen Haddad Gary A Heiman Sian M J Hemmings Ana G Hounie Cornelia Illmann Joseph Jankovic Michael A Jenike James L Kennedy Robert A King Barbara Kremeyer Roger Kurlan Nuria Lanzagorta Marion Leboyer James F Leckman Leonhard Lennertz Chunyu Liu Christine Lochner Thomas L Lowe Fabio Macciardi James T McCracken Lauren M McGrath Sandra C Mesa Restrepo Rainald Moessner Jubel Morgan Heike Muller Dennis L Murphy Allan L Naarden William Cornejo Ochoa Roel A Ophoff Lisa Osiecki Andrew J Pakstis Michele T Pato Carlos N Pato John Piacentini Christopher Pittenger Yehuda Pollak Scott L Rauch Tobias J Renner Victor I Reus Margaret A Richter Mark A Riddle Mary M Robertson Roxana Romero Maria C Rosàrio David Rosenberg Guy A Rouleau Stephan Ruhrmann Andres Ruiz-Linares Aline S Sampaio Jack Samuels Paul Sandor Brooke Sheppard Harvey S Singer Jan H Smit Dan J Stein E Strengman Jay A Tischfield Ana V Valencia Duarte Homero Vallada Filip Van Nieuwerburgh Jeremy Veenstra-Vanderweele Susanne Walitza Ying Wang Jens R Wendland Herman G M Westenberg Yin Yao Shugart Euripedes C Miguel William McMahon Michael Wagner Humberto Nicolini Danielle Posthuma Gregory L Hanna Peter Heutink Damiaan Denys Paul D Arnold Ben A Oostra Gerald Nestadt Nelson B Freimer David L Pauls Naomi R Wray S Evelyn Stewart Carol A Mathews James A Knowles Nancy J Cox Jeremiah M Scharf

PLoS Genet 2013 Oct 24;9(10):e1003864. Epub 2013 Oct 24.

Section of Genetic Medicine, Department of Medicine, University of Chicago, Chicago, Illinois, United States of America.

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http://dx.doi.org/10.1371/journal.pgen.1003864DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812053PMC
October 2013

Quantitative association of tobacco smoking with the risk of nasopharyngeal carcinoma: a comprehensive meta-analysis of studies conducted between 1979 and 2011.

Am J Epidemiol 2013 Aug 19;178(3):325-38. Epub 2013 Jun 19.

State Key Laboratory of Oncology in Southern China, Department of Experimental Research, Sun Yat-Sen University Cancer Center, Guangzhou 510060, People’s Republic of China.

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http://dx.doi.org/10.1093/aje/kws479DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727336PMC
August 2013

Amish revisited: next-generation sequencing studies of psychiatric disorders among the Plain people.

Trends Genet 2013 Jul 17;29(7):412-8. Epub 2013 Feb 17.

Human Genetics Branch, National Institute of Mental Health (NIMH) Intramural Research Program, National Institutes of Health (NIH), US Department of Health and Human Services, Bethesda, MD, USA.

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http://dx.doi.org/10.1016/j.tig.2013.01.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941079PMC
July 2013

Functional polymorphism in the 5'-UTR of CR2 is associated with susceptibility to nasopharyngeal carcinoma.

Oncol Rep 2013 Jul 23;30(1):11-6. Epub 2013 Apr 23.

College of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, P.R. China.

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http://dx.doi.org/10.3892/or.2013.2421DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3729234PMC
July 2013

Detecting rare variants for quantitative traits using nuclear families.

Hum Hered 2012 12;73(3):148-58. Epub 2012 Jun 12.

Division of Intramural Division Program, National Institute of Mental Health, National Institute of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1159/000338439DOI Listing
November 2012

Weighted pedigree-based statistics for testing the association of rare variants.

BMC Genomics 2012 Nov 24;13:667. Epub 2012 Nov 24.

Unit of Statistical Genomics, Division of Intramural Division Program, National Institute of Mental Health, National Institute of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1186/1471-2164-13-667DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827928PMC
November 2012

Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer.

Authors:
Christopher A Maxwell Javier Benítez Laia Gómez-Baldó Ana Osorio Núria Bonifaci Ricardo Fernández-Ramires Sylvain V Costes Elisabet Guinó Helen Chen Gareth J R Evans Pooja Mohan Isabel Català Anna Petit Helena Aguilar Alberto Villanueva Alvaro Aytes Jordi Serra-Musach Gad Rennert Flavio Lejbkowicz Paolo Peterlongo Siranoush Manoukian Bernard Peissel Carla B Ripamonti Bernardo Bonanni Alessandra Viel Anna Allavena Loris Bernard Paolo Radice Eitan Friedman Bella Kaufman Yael Laitman Maya Dubrovsky Roni Milgrom Anna Jakubowska Cezary Cybulski Bohdan Gorski Katarzyna Jaworska Katarzyna Durda Grzegorz Sukiennicki Jan Lubiński Yin Yao Shugart Susan M Domchek Richard Letrero Barbara L Weber Frans B L Hogervorst Matti A Rookus J Margriet Collee Peter Devilee Marjolijn J Ligtenberg Rob B van der Luijt Cora M Aalfs Quinten Waisfisz Juul Wijnen Cornelis E P van Roozendaal Douglas F Easton Susan Peock Margaret Cook Clare Oliver Debra Frost Patricia Harrington D Gareth Evans Fiona Lalloo Rosalind Eeles Louise Izatt Carol Chu Diana Eccles Fiona Douglas Carole Brewer Heli Nevanlinna Tuomas Heikkinen Fergus J Couch Noralane M Lindor Xianshu Wang Andrew K Godwin Maria A Caligo Grazia Lombardi Niklas Loman Per Karlsson Hans Ehrencrona Anna von Wachenfeldt Rosa Bjork Barkardottir Ute Hamann Muhammad U Rashid Adriana Lasa Trinidad Caldés Raquel Andrés Michael Schmitt Volker Assmann Kristen Stevens Kenneth Offit João Curado Hagen Tilgner Roderic Guigó Gemma Aiza Joan Brunet Joan Castellsagué Griselda Martrat Ander Urruticoechea Ignacio Blanco Laima Tihomirova David E Goldgar Saundra Buys Esther M John Alexander Miron Melissa Southey Mary B Daly Rita K Schmutzler Barbara Wappenschmidt Alfons Meindl Norbert Arnold Helmut Deissler Raymonda Varon-Mateeva Christian Sutter Dieter Niederacher Evgeny Imyamitov Olga M Sinilnikova Dominique Stoppa-Lyonne Sylvie Mazoyer Carole Verny-Pierre Laurent Castera Antoine de Pauw Yves-Jean Bignon Nancy Uhrhammer Jean-Philippe Peyrat Philippe Vennin Sandra Fert Ferrer Marie-Agnès Collonge-Rame Isabelle Mortemousque Amanda B Spurdle Jonathan Beesley Xiaoqing Chen Sue Healey Mary Helen Barcellos-Hoff Marc Vidal Stephen B Gruber Conxi Lázaro Gabriel Capellá Lesley McGuffog Katherine L Nathanson Antonis C Antoniou Georgia Chenevix-Trench Markus C Fleisch Víctor Moreno Miguel Angel Pujana

PLoS Biol 2011 Nov 15;9(11):e1001199. Epub 2011 Nov 15.

Translational Research Laboratory, Catalan Institute of Oncology, Bellvitge Biomedical Research Institute-IDIBELL, L'Hospitalet, Catalonia, Spain.

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http://dx.doi.org/10.1371/journal.pbio.1001199DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3217025PMC
November 2011

Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives.

BMC Proc 2011 Nov 29;5 Suppl 9:S76. Epub 2011 Nov 29.

Mood and Anxiety Section, Human Genetics Branch, National Institute of Mental Health, National Institutes of Health, 35 Convent Drive, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1186/1753-6561-5-S9-S76DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287916PMC
November 2011

Elevated Epstein-Barr virus seroreactivity among unaffected members of families with nasopharyngeal carcinoma.

J Med Virol 2011 Oct;83(10):1792-8

State Key Laboratory of Oncology in South China, Department of Experimental Research, Sun Yat-Sen University Cancer Center, Guangzhou, China.

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http://doi.wiley.com/10.1002/jmv.22121
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October 2011

Human genetic variants of homologous recombination repair genes first found to be associated with Epstein-Barr virus antibody titers in healthy Cantonese.

Int J Cancer 2011 Sep 12;129(6):1459-66. Epub 2011 Jan 12.

State Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, China.

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http://doi.wiley.com/10.1002/ijc.25759
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http://dx.doi.org/10.1002/ijc.25759DOI Listing
September 2011

A gender-specific association of CNV at 6p21.3 with NPC susceptibility.

Hum Mol Genet 2011 Jul 2;20(14):2889-96. Epub 2011 May 2.

Genome Medicine Core, Chang Gung Molecular Medicine Research Center, Graduate Institute of Biomedical Sciences, Chang Gung University, No. 259 Wen-Hwa 1st Road, Kwei-shan,Taoyuan 333, Taiwan.

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http://dx.doi.org/10.1093/hmg/ddr191DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3146013PMC
July 2011

Genetic polymorphisms in DNA double-strand break repair genes XRCC5, XRCC6 and susceptibility to hepatocellular carcinoma.

Carcinogenesis 2011 Apr 8;32(4):530-6. Epub 2011 Feb 8.

State Key Laboratory of Genetic Engineering, School of Life Sciences and Institutes of Biomedical Sciences, Fudan University, 220 Handan Road, Shanghai 200433 China.

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https://academic.oup.com/carcin/article-lookup/doi/10.1093/c
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http://dx.doi.org/10.1093/carcin/bgr018DOI Listing
April 2011

Comprehensive pathway-based association study of DNA repair gene variants and the risk of nasopharyngeal carcinoma.

Cancer Res 2011 Apr 2;71(8):3000-8. Epub 2011 Mar 2.

State Key Laboratory of Oncology in South China, Department of Experimental Research, Sun Yat-Sen University Cancer Center, Guangzhou, China.

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http://dx.doi.org/10.1158/0008-5472.CAN-10-0469DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383064PMC
April 2011

GWAS signals across the HLA regions: revealing a clue for common etiology underlying infectious tumors and other immunity diseases.

Chin J Cancer 2011 Apr;30(4):226-30

Unit of Statistical Genomics, Intramural Research Program, National Institute of Mental Health, National Institute of Health, Bethesda, Maryland 20892, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3381606PMC
April 2011

Possible association between polymorphisms of human vascular endothelial growth factor A gene and susceptibility to glioma in a Chinese population.

Int J Cancer 2011 Jan;128(1):166-75

State Key Laboratory of Genetic Engineering, Center for Fudan-VARI Genetics Epidemiology and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, Shanghai, China.

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http://dx.doi.org/10.1002/ijc.25306DOI Listing
January 2011

Cruciferous vegetable intake and lung cancer risk: a nested case-control study matched on cigarette smoking.

Cancer Epidemiol Biomarkers Prev 2010 Oct 14;19(10):2534-40. Epub 2010 Sep 14.

Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, USA.

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http://dx.doi.org/10.1158/1055-9965.EPI-10-0475DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2952042PMC
October 2010

Mapping human genetic diversity in Asia.

Science 2009 Dec;326(5959):1541-5

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http://dx.doi.org/10.1126/science.1177074DOI Listing
December 2009

Hypothesis-driven candidate gene association studies: practical design and analytical considerations.

Am J Epidemiol 2009 Oct 17;170(8):986-93. Epub 2009 Sep 17.

Department of Radiation Medicine, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20057, USA.

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http://dx.doi.org/10.1093/aje/kwp242DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2765367PMC
October 2009

Copy number variants of GSTM1 and GSTT1 in relation to lung cancer risk in a prospective cohort study.

Ann Epidemiol 2009 Aug 25;19(8):546-52. Epub 2009 Apr 25.

Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.

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http://dx.doi.org/10.1016/j.annepidem.2009.03.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720160PMC
August 2009

Common genetic variations of the cytochrome P450 1A1 gene and risk of hepatocellular carcinoma in a Chinese population.

Eur J Cancer 2009 May 26;45(7):1239-1247. Epub 2008 Dec 26.

State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University, 220 Handan Rd., Shanghai 200433, PR China.

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http://dx.doi.org/10.1016/j.ejca.2008.11.007DOI Listing
May 2009

A simulation study of control sampling methods for nested case-control studies of genetic and molecular biomarkers and prostate cancer progression.

Cancer Epidemiol Biomarkers Prev 2009 Mar 3;18(3):706-11. Epub 2009 Mar 3.

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, and Department of Medicine, Saint Agnes Hospital, Room E6132, 615 North Wolfe Street, Baltimore, MD 21205, USA.

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http://dx.doi.org/10.1158/1055-9965.EPI-08-0839DOI Listing
March 2009

Contributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohn's disease risk in a population-based case-control study: evidence of gene-gene interactions.

Inflamm Bowel Dis 2008 Nov;14(11):1528-41

Harvey M. and Lyn P. Meyerhoff Inflammatory Bowel Disease Center, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, USA.

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http://dx.doi.org/10.1002/ibd.20512DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3336049PMC
November 2008

Polymorphisms of LIG4 and XRCC4 involved in the NHEJ pathway interact to modify risk of glioma.

Hum Mutat 2008 Mar;29(3):381-9

State Key Laboratory of Genetic Engineering, School of Life Sciences, Fudan University, Shanghai, China.

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http://dx.doi.org/10.1002/humu.20645DOI Listing
March 2008

Family-based linkage disequilibrium tests using general pedigrees.

Methods Mol Biol 2007 ;376:141-9

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

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http://dx.doi.org/10.1007/978-1-59745-389-9_10DOI Listing
December 2007

Polymorphic variants in alpha-methylacyl-CoA racemase and prostate cancer.

Prostate 2007 Oct;67(14):1487-97

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1002/pros.20635DOI Listing
October 2007

Tagging SNPs in non-homologous end-joining pathway genes and risk of glioma.

Carcinogenesis 2007 Sep 26;28(9):1906-13. Epub 2007 Mar 26.

State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences and Institutes for Biomedical Sciences, Fudan University, 220 Handan Road, Shanghai 200433, China.

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http://dx.doi.org/10.1093/carcin/bgm073DOI Listing
September 2007

Variants in the alpha-Methylacyl-CoA racemase gene and the association with advanced distal colorectal adenoma.

Cancer Epidemiol Biomarkers Prev 2007 Aug;16(8):1536-42

Divison of Cancer Epidemiology and Genetics, Department of Health and Human Services, National Cancer Institute, 6120 Executive Boulevard, EPS Rm 8113, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1158/1055-9965.EPI-07-0117DOI Listing
August 2007

A population-based case-control study of CARD15 and other risk factors in Crohn's disease and ulcerative colitis.

Am J Gastroenterol 2007 Feb 13;102(2):313-23. Epub 2006 Nov 13.

Harvey M. and Lyn P. Meyerhoff Inflammatory Bowel Disease Center, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, USA.

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http://dx.doi.org/10.1111/j.1572-0241.2006.00926.xDOI Listing
February 2007

Effect of the peroxisome proliferators-activated receptor (PPAR) gamma 3 gene on BMI in 1,210 school students from Morelos, Mexico.

Pac Symp Biocomput 2006 :467-77

Department of Social Medicine, University of Bristol, Bristol, UK.

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January 2007