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APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study

Molecular psychiatry, 2014-03, Vol.19 (3), p.351-357

2014

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Oculomotor control in asymptomatic and recently diagnosed individuals with the genetic marker for Huntington’s disease

Vision research (Oxford), 2004-10, Vol.44 (23), p.2729-2736

2004

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Genetic Predisposition to External Apical Root Resorption in Orthodontic Patients: Linkage of Chromosome-18 Marker

Journal of dental research, 2003-05, Vol.82 (5), p.356-360

2003

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Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension

American journal of respiratory and critical care medicine, 1995-07, Vol.152 (1), p.93

1995

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The Alzheimer's Disease Sequencing Project: Study design and sample selection

Neurology. Genetics, 2017-10, Vol.3 (5), p.e194-e194

2017

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FASTKD2 is associated with memory and hippocampal structure in older adults

Molecular psychiatry, 2015-10, Vol.20 (10), p.1197-1204

2015

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Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or women

Osteoporosis international, 2006-04, Vol.17 (4), p.587-592

2006

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Alcohol dehydrogenase-22 allele is associated with decreased prevalence of fetal alcohol syndrome in the mixed-ancestry population of the Western Cape Province, South Africa

Alcoholism, clinical and experimental research, 2001-12, Vol.25 (12), p.1719-1722

2001

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Association of the Angiotensinogen Gene to Serum Angiotensinogen in Blacks and Whites

Hypertension (Dallas, Tex. 1979), 1997-05, Vol.29 (5), p.1078-1082

1997

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A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

Acta neuropathologica, 2019-08, Vol.138 (2), p.237-250

2019

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Genetic Variants Associated with Circulating Fibroblast Growth Factor 23

Journal of the American Society of Nephrology, 2018-10, Vol.29 (10), p.2583-2592

2018

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Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

Acta neuropathologica, 2020-05, Vol.139 (5), p.959-962

2020

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Alcohol Dehydrogenase-22 Allele is Associated With Decreased Prevalence of Fetal Alcohol Syndrome in the Mixed-Ancestry Population of the Western Cape Province, South Africa

Alcoholism, clinical and experimental research, 2001-12, Vol.25 (12), p.1719-1722

2001

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The Presence of Genetic Anticipation Suggests That the Molecular Basis of Familial Primary Pulmonary Hypertension May Be Trinucleotide Repeat Expansion

Chest, 1997-06, Vol.111 (6), p.82S-83S

1997

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Genetic predisposition to external apical root resorption

American journal of orthodontics and dentofacial orthopedics, 2003-03, Vol.123 (3), p.242-252

2003

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Human ALOX12, but Not ALOX15, Is Associated With BMD in White Men and Women

Journal of bone and mineral research, 2006-04, Vol.21 (4), p.556-564

2006

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Polymorphisms in the Estrogen Receptor β (ESR2) Gene Are Associated with Bone Mineral Density in Caucasian Men and Women

The journal of clinical endocrinology and metabolism, 2005-11, Vol.90 (11), p.5921-5927

2005

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Confirmation of Linkage to Chromosome 1q for Peak Vertebral Bone Mineral Density in Premenopausal White Women

American journal of human genetics, 2004-02, Vol.74 (2), p.223-228

2004

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Heritability of Changes in Bone Size and Bone Mass With Age in Premenopausal White Sisters

Journal of bone and mineral research, 2006-07, Vol.21 (7), p.1121-1125

2006

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Root resorption associated with orthodontic force in inbred mice: genetic contributions

European journal of orthodontics, 2006-02, Vol.28 (1), p.13-19

2006

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Longitudinal Associations of Blood Phosphorylated Tau181 and Neurofilament Light Chain With Neurodegeneration in Alzheimer Disease

JAMA neurology, 2021-04, Vol.78 (4), p.396

2021

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Alzheimer's disease: analyzing the missing heritability

PloS one, 2013-11, Vol.8 (11), p.e79771-e79771

2013

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Assessment of the genetic variance of late-onset Alzheimer's disease

Neurobiology of aging, 2016-05, Vol.41, p.200.e13-200.e20

2016

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APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study

Oculomotor control in asymptomatic and recently diagnosed individuals with the genetic marker for Huntington’s disease

Genetic Predisposition to External Apical Root Resorption in Orthodontic Patients: Linkage of Chromosome-18 Marker

Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension

The Alzheimer's Disease Sequencing Project: Study design and sample selection

FASTKD2 is associated with memory and hippocampal structure in older adults

Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or women

Alcohol dehydrogenase-22 allele is associated with decreased prevalence of fetal alcohol syndrome in the mixed-ancestry population of the Western Cape Province, South Africa

Association of the Angiotensinogen Gene to Serum Angiotensinogen in Blacks and Whites

A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

Genetic Variants Associated with Circulating Fibroblast Growth Factor 23

Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

Alcohol Dehydrogenase-22 Allele is Associated With Decreased Prevalence of Fetal Alcohol Syndrome in the Mixed-Ancestry Population of the Western Cape Province, South Africa

The Presence of Genetic Anticipation Suggests That the Molecular Basis of Familial Primary Pulmonary Hypertension May Be Trinucleotide Repeat Expansion

Genetic predisposition to external apical root resorption

Human ALOX12, but Not ALOX15, Is Associated With BMD in White Men and Women

Polymorphisms in the Estrogen Receptor β (ESR2) Gene Are Associated with Bone Mineral Density in Caucasian Men and Women

Confirmation of Linkage to Chromosome 1q for Peak Vertebral Bone Mineral Density in Premenopausal White Women

Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees

Heritability of Changes in Bone Size and Bone Mass With Age in Premenopausal White Sisters

Root resorption associated with orthodontic force in inbred mice: genetic contributions

Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction

Longitudinal Associations of Blood Phosphorylated Tau181 and Neurofilament Light Chain With Neurodegeneration in Alzheimer Disease

Alzheimer's disease: analyzing the missing heritability

Assessment of the genetic variance of late-onset Alzheimer's disease

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