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Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes

Human molecular genetics, 2011-04, Vol.20 (7), p.1456-1466

2011

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Bone marrow-derived epithelial cells and hair follicle stem cells contribute to development of chronic cutaneous neoplasms

Nature communications, 2018-12, Vol.9 (1), p.5293-15, Article 5293

2018

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TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data

BMC bioinformatics, 2012-01, Vol.13 (1), p.13-13, Article 13

2012

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A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females

Nature communications, 2015-03, Vol.6 (1), p.6452-6452, Article 6452

2015

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Abstract LB-039: Chronic inflammation-mediated contribution of bone marrow-derived epithelial cells and hair follicle stem cells to development of cutaneous neoplasms

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.LB-039-LB-039

2019

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Neurocognitive endophenotypes: an update on the Field

International journal of psychological research, 2016-01, Vol.9 (1), p.6-8

2016

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Neurocognitive Endophenotypes: an update on the field: Endofenotipos Neurocognitivos/una actualizacion en el area

International journal of psychological research, 2016-01, Vol.9 (1), p.6

2016

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A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups

Journal of medical genetics, 2014-06, Vol.51 (6), p.401-406

2014

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Chromatin Profiling Reveals Regulatory Network Shifts and a Protective Role for Hepatocyte Nuclear Factor 4α during Colitis

Molecular and cellular biology, 2014-09, Vol.34 (17), p.3291-3304

2014

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Heroin addiction in African Americans: a hypothesis‐driven association study

Genes, brain and behavior, 2009-07, Vol.8 (5), p.531-540

2009

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Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata

American journal of human genetics, 2007-02, Vol.80 (2), p.316-328

2007

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Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach

European archives of psychiatry and clinical neuroscience, 2018-04, Vol.268 (3), p.301-316

2018

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IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants

Pediatric research, 2012-01, Vol.71 (1), p.107-114

2012

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An Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of Inheritance

Human heredity, 2016-01, Vol.81 (4), p.194-209

2016

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EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity

Physiological genomics, 2010-03, Vol.41 (1), p.71-77

2010

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IL-18R1 and IL-18RAP SNPs may associate with Bronchopulmonary Dysplasia in African American infants

Pediatric research, 2012-01, Vol.71 (1), p.107-114

2012

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A novel method for analyzing genetic association with longitudinal phenotypes

Statistical applications in genetics and molecular biology, 2013-03, Vol.12 (2), p.241-261

2013

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Evidence for association of two variants of the nociceptin/orphanin FQ receptor gene OPRL1 with vulnerability to develop opiate addiction in Caucasians

Psychiatric genetics, 2010-04, Vol.20 (2), p.65-72

2010

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Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities

BMC proceedings, 2014, Vol.8 (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo), p.S81-S81, Article S81

2014

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Single-Variant and Multi-Variant Trend Tests for Genetic Association with Next-Generation Sequencing That Are Robust to Sequencing Error

Human heredity, 2012-01, Vol.74 (3/4), p.172-183

2012

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A Cost-Effective Statistical Method to Correct for Differential Genotype Misclassification When Performing Case-Control Genetic Association

Human heredity, 2010-01, Vol.70 (2), p.102-108

2010

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Neurocognitive endophenotypes: an update on the Field

International journal of psychological research, 2016-01, Vol.9 (1)

2016

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Endofenotipos neurocognitivos: una actualización en el área

International journal of psychological research, 2016-01, Vol.9 (1), p.6

2016

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Beta 2 adrenergic receptor polymorphisms in cystic fibrosis

Pediatric pulmonology, 2005-06, Vol.39 (6), p.544-550

2005

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Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes

Bone marrow-derived epithelial cells and hair follicle stem cells contribute to development of chronic cutaneous neoplasms

TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data

Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis

A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females

Abstract LB-039: Chronic inflammation-mediated contribution of bone marrow-derived epithelial cells and hair follicle stem cells to development of cutaneous neoplasms

Neurocognitive endophenotypes: an update on the Field

Neurocognitive Endophenotypes: an update on the field: Endofenotipos Neurocognitivos/una actualizacion en el area

A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups

Chromatin Profiling Reveals Regulatory Network Shifts and a Protective Role for Hepatocyte Nuclear Factor 4α during Colitis

Heroin addiction in African Americans: a hypothesis‐driven association study

Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata

Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach

IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants

An Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of Inheritance

EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity

IL-18R1 and IL-18RAP SNPs may associate with Bronchopulmonary Dysplasia in African American infants

A novel method for analyzing genetic association with longitudinal phenotypes

Evidence for association of two variants of the nociceptin/orphanin FQ receptor gene OPRL1 with vulnerability to develop opiate addiction in Caucasians

Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities

Single-Variant and Multi-Variant Trend Tests for Genetic Association with Next-Generation Sequencing That Are Robust to Sequencing Error

A Cost-Effective Statistical Method to Correct for Differential Genotype Misclassification When Performing Case-Control Genetic Association

Neurocognitive endophenotypes: an update on the Field

Endofenotipos neurocognitivos: una actualización en el área

Beta 2 adrenergic receptor polymorphisms in cystic fibrosis

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