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All papers authored by Desmond Campbell

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2022 Richard J. Shaw

ORCID

, Katie L. Harron

ORCID

, Julia M. Pescarini

ORCID

, Elzo Pereira Pinto Junior

ORCID

ORCID

, Andressa N. Siroky

ORCID

, Desmond Campbell

ORCID

ORCID

, Maria Yury Ichihara

ORCID

, Alastair H. Leyland

ORCID

, Mauricio L. Barreto

ORCID

, Srinivasa Vittal Katikireddi

ORCID

Biases arising from linked administrative data for epidemiological research: a conceptual framework from registration to analyses

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2016 John K. L. Wong, Desmond Campbell

ORCID

, Ngoc Diem Ngo, Fanny Yeung, Guo Cheng, Clara S. M. Tang, Patrick H. Y. Chung, Ngoc Son Tran, Man-Ting So, Stacey S. Cherny

ORCID

, Pak C. Sham, Paul K. Tam, Maria-Mercè Garcia-Barcelo

Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

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Robert Milan Porsch

ORCID

, Elisa Merello, Patrizia De Marco, Guo Cheng, Laura Rodriguez, Manting So, Pak C. Sham, Paul K. Tam, Valeria Capra, Valeria Carpa, Stacey S. Cherny

ORCID

, Maria-Mercè Garcia-Barcelo, Desmond D. Campbell

ORCID

Sacral agenesis: a pilot whole exome sequencing and copy number study

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Peng Zhou, Ran Wei, Zhenkui Guo, Haining Zhu, Qi Li, Xiaoqun Xu, Junfu Wang, Meng Luan, Xing Chen, Gang Chen, Desmond Campbell

ORCID

A single nucleotide variant in HNF-1β is associated with maturity-onset diabetes of the young in a large Chinese family

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Timothy Shin Heng Mak, Sht Mak, Johnny Sheung Him Kwan, Sh Kwan, Desmond Dedalus Campbell

ORCID

, Pak Chung Sham

Local True Discovery Rate Weighted Polygenic Scores Using GWAS Summary Data

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Yan Li, Dino Samartzis, Desmond D. Campbell

ORCID

, Stacey Ss Cherny

ORCID

, Kmc Cheung, Keith D. Kdk Luk, Jaro Karppinen, Youqiang Song

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, Kse Cheah, Danny Chan, Pc Sham

Two subtypes of intervertebral disc degeneration distinguished by large-scale population-based study

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2015 Desmond D. Campbell

ORCID

, Robert M. Porsch, Stacey Ss Cherny

ORCID

, Valeria Capra, Elisa Merello, Patrizia De Marco, Pak C. Sham, Maria-Mercè Garcia-Barceló

Cost effective assay choice for rare disease study designs

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2014 T. Toulopoulou, N. van Haren, X. Zhang, Nv Haren, X. Zhou, Pc C. Sham, Ss S. Cherny

ORCID

, D. D. Campbell

ORCID

ORCID

, R. Murray, Di I. Boomsma, Hilleke E. Hulshoff Pol, Hh H. Pol, R. Brouwer, H. Schnack and 6 other authors

Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort

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Shugart Yy, Dongmei Yu, Carol A. Mathews, Scharf Jm, Jeremiah M. Scharf, Neale Bm, Benjamin M. Neale, Lea K. Davis, Davis Lk, Eric R. Gamazon, Eske M. Derks, Derks Em, Patrick Evans, Christopher K. Edlund, Edlund Ck and 204 other authors

Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette's Syndrome and OCD

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Conrad Iyegbe, Desmond Campbell

ORCID

, Amy Butler, Pak Sham, Olesya Ajnakina, James B. Kirkbride

The emerging molecular architecture of schizophrenia, polygenic risk scores and the clinical implications for gXe research

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Desmond Dedalus Campbell

ORCID

Error in sample size formula

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Hannah Dickson

ORCID

, Alexis E. Cullen, Abraham Reichenberg, Sheilagh Hodgins, Desmond D. Campbell

ORCID

, R. M. Morris, Robin G. Morris, K. R. Larurens, Kristin R. Laurens

ORCID

Cognitive impairment among children at-risk for schizophrenia

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2013 Filip van Nieuwerburgh, Matthew C. Keller, Lea K. Davis, Dongmei Yu, Clare L. Keenan, Eric R. Gamazon, Anuar I. Konkashbaev, Eske M. Derks, Benjamin M. Neale, Jian Yang

ORCID

, Sh Hong Lee, Patrick Evans, Cathy L. Barr, Laura Bellodi, Fortu Benarroch and 121 other authors

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

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Ge Zhang, Abhishek Nag, Elena G. Bochukova, Barbara Kremeyer, Desmond D. Campbell

ORCID

, Heike Muller, Ana V. Valencia-Duarte, Julio Cardona, Isabel C. Rivas, Sandra C. Mesa, Mauricio Cuartas, Jharley Garcia, Gabriel Bedoya, William Cornejo, Luis D. Herrera and 17 other authors

CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1

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2012 Jm M. Scharf, D. Yu, Ca A. Mathews, Bm M. Neale, Se E. Stewart, Ja A. Fagerness, P. Evans, E. Gamazon, Ck K. Edlund, Sk K. Service, A. Tikhomirov, L. Osiecki, C. Illmann, A. Pluzhnikov, A. Konkashbaev and 88 other authors

Genome-wide association study of Tourette's syndrome.

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Desmond D. Campbell

ORCID

, Maria V. Parra, Constanza Duque, Natalia Gallego, Liliana Franco, Arti Tandon, Tábita Hünemeier, Cátira Bortolini, Alberto Villegas, Gabriel Bedoya, Mark I. McCarthy, Alkes Price, David Reich, Andrés Ruiz-Linares

ORCID

Amerind Ancestry, Socioeconomic Status and the Genetics of Type 2 Diabetes in a Colombian Population

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Patricia Huezo-Diaz, Nader Perroud, Edgar P. Spencer, Robert Peter Smith, Sarah S. Sim, Susanne S. Virding, Rudolf Uher, Cerisse Gunasinghe, Jonathon Gray, Desmond D. Campbell

ORCID

, Joanna Wiktoria Hauser, Wolfgang W. Maier, Andrej Marusic, Marcella Rietschel, Jorge Coarasa Perez and 8 other authors

CYP2C19 genotype predicts steady state escitalopram concentration in GENDEP

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David Reich, Nick Patterson, Desmond Campbell

ORCID

, Arti Tandon, Stéphane Mazieres, Nicolas Ray, Mv Parra, Winston Rojas, Constanza Duque, Natalia Mesa, Lf García, Omar Triana, Silvia Blair, Amanda Maestre, Jc Dib and 49 other authors

Reconstructing Native American population history

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2009 Nader Perroud, Rudolf Uher, Andrej Marusic, Marcella Rietschel, Ole Mors, Neven Henigsberg, Joanna Wiktoria Hauser, Wolfgang Maier, Daniel Souery, Anna Placentino, Aleksandra Szczepankiewicz, Lisbeth Jorgensen, Jana Strohmaier, Astrid Zobel, Caterina Giovannini and 8 other authors

Suicidal ideation during treatment of depression with escitalopram and nortriptyline in Genome-Based Therapeutic Drugs for Depression (GENDEP): a clinical trial

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Desmond D. Campbell

ORCID

, Pak C. Sham, Jo Knight, Harvey Wickham, Sabine Landau

Software for generating liability distributions for pedigrees conditional on their observed disease states and covariates

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