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Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas

Nature genetics, 2013-02, Vol.45 (2), p.136-144

2013

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Variants on chromosome 4q21 near PKD2 and SIBLINGs are associated with dental caries

Journal of human genetics, 2017-04, Vol.62 (4), p.491-496

2017

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Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor

Nature genetics, 2008-11, Vol.40 (11), p.1329-1334

2008

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Dopamine system genes and attention deficit hyperactivity disorder: a meta-analysis

Psychiatric genetics, 2002-12, Vol.12 (4), p.207-215

2002

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Genome Scan for Loci Involved in Cleft Lip With or Without Cleft Palate, in Chinese Multiplex Families

American journal of human genetics, 2002-08, Vol.71 (2), p.349-364

2002

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Genome-wide linkage survey for genetic loci that influence the development of depressive disorders in families with recurrent, early-onset, major depression

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2003-11, Vol.123B (1), p.1-18

2003

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Association of the serotonin transporter gene with sudden infant death syndrome: A haplotype analysis

American journal of medical genetics, 2003-10, Vol.122A (3), p.238-245

2003

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Sudden infant death syndrome: Association with a promoter polymorphism of the serotonin transporter gene

American journal of medical genetics, 2003-03, Vol.117A (3), p.268-274

2003

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Genetic linkage of region containing the CREB1 gene to depressive disorders in women from families with recurrent, early-onset, major depression

American journal of medical genetics, 2002-12, Vol.114 (8), p.980-987

2002

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Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio

American journal of medical genetics, 2004-03, Vol.125A (2), p.135-144

2004

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Genome-wide linkage survey for genetic loci that affect the risk of suicide attempts in families with recurrent, early-onset, major depression

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2004-08, Vol.129B (1), p.47-54

2004

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Installing oncofertility programs for common cancers in optimum resource settings (Repro-Can-OPEN Study Part II): a committee opinion

Journal of assisted reproduction and genetics, 2021, Vol.38 (1), p.163-176

2021

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Three-dimensional morphometric analysis of craniofacial shape in the unaffected relatives of individuals with nonsyndromic orofacial clefts: A possible marker for genetic susceptibility

American journal of medical genetics. Part A, 2008-02, Vol.146A (4), p.409-420

2008

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Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate

American journal of medical genetics. Part A, 2007-06, Vol.143A (11), p.1143-1149

2007

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3′ UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: Haplotype analysis

American journal of medical genetics. Part A, 2006-07, Vol.140A (13), p.1453-1457

2006

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Identifying genomic regions for fine-mapping using genome scan meta-analysis (GSMA) to identify the minimum regions of maximum significance (MRMS) across populations

BMC genetics, 2005-12, Vol.6 Suppl 1, p.S42

2005

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Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene

American journal of medical genetics. Part A, 2006-08, Vol.140A (15), p.1687-1691

2006

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COGENT (COlorectal cancer GENeTics) revisited

Mutagenesis, 2012-03, Vol.27 (2), p.143-151

Houlston, Richard S

2012

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Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome

American journal of medical genetics. Part A, 2006-07, Vol.140A (13), p.1447-1452

2006

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Segregation analysis of attention deficit hyperactivity disorder

American journal of medical genetics, 1999-02, Vol.88 (1), p.71-78

1999

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Quantitative Trait Linkage Analysis of the Liability Underlying a Common Oligogenic Disease

Genetic epidemiology, 2001, Vol.21 (S1), p.S720-S725

2001

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Case/control family study of autonomic nervous system dysfunction in idiopathic congenital central hypoventilation syndrome

American journal of medical genetics, 2001-05, Vol.100 (3), p.237-245

2001

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Von Hippel-Lindau disease : identification of deletion mutations by pulsed-field gel electrophoresis

Human genetics, 1993-12, Vol.92 (6), p.605-614

1993

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Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas

Meta-Analysis of 13 Genome Scans Reveals Multiple Cleft Lip/Palate Genes with Novel Loci on 9q21 and 2q32-35

Variants on chromosome 4q21 near PKD2 and SIBLINGs are associated with dental caries

Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor

Dopamine system genes and attention deficit hyperactivity disorder: a meta-analysis

Genome Scan for Loci Involved in Cleft Lip With or Without Cleft Palate, in Chinese Multiplex Families

Genome Scan, Fine-Mapping, and Candidate Gene Analysis of Non-Syndromic Cleft Lip with or without Cleft Palate Reveals Phenotype-Specific Differences in Linkage and Association Results

Genome-wide linkage survey for genetic loci that influence the development of depressive disorders in families with recurrent, early-onset, major depression

Association of the serotonin transporter gene with sudden infant death syndrome: A haplotype analysis

Sudden infant death syndrome: Association with a promoter polymorphism of the serotonin transporter gene

Genetic linkage of region containing the CREB1 gene to depressive disorders in women from families with recurrent, early-onset, major depression

Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio

Genome-wide linkage survey for genetic loci that affect the risk of suicide attempts in families with recurrent, early-onset, major depression

Installing oncofertility programs for common cancers in optimum resource settings (Repro-Can-OPEN Study Part II): a committee opinion

Three-dimensional morphometric analysis of craniofacial shape in the unaffected relatives of individuals with nonsyndromic orofacial clefts: A possible marker for genetic susceptibility

Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate

3′ UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: Haplotype analysis

Identifying genomic regions for fine-mapping using genome scan meta-analysis (GSMA) to identify the minimum regions of maximum significance (MRMS) across populations

Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene

COGENT (COlorectal cancer GENeTics) revisited

Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome

Segregation analysis of attention deficit hyperactivity disorder

Quantitative Trait Linkage Analysis of the Liability Underlying a Common Oligogenic Disease

Case/control family study of autonomic nervous system dysfunction in idiopathic congenital central hypoventilation syndrome

Von Hippel-Lindau disease : identification of deletion mutations by pulsed-field gel electrophoresis

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