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A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records

PLoS genetics, 2016-10, Vol.12 (10), p.e1006371-e1006371

2016

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The role of the dopamine transporter (DAT) in the development of PTSD in preschool children

Journal of traumatic stress, 2009-12, Vol.22 (6), p.534-539

2009

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Dominant and recessive deafness caused by mutations of a novel gene, TMC1 , required for cochlear hair-cell function

Nature genetics, 2002-03, Vol.30 (3), p.277-284

2002

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Harmonin (Ush1c) is required in zebrafish Müller glial cells for photoreceptor synaptic development and function

Disease models & mechanisms, 2011-11, Vol.4 (6), p.786-800

2011

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HPPD: A newly recognized autosomal dominant disorder involving hypertelorism, preauricular sinus, punctal pits, and deafness mapping to chromosome 14q31

American journal of medical genetics. Part A, 2011-05, Vol.155A (5), p.976-985

2011

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Multi-site diagnosis and management of 260 patients with Auditory Neuropathy/Dys-synchrony (Auditory Neuropathy Spectrum Disorder)

International journal of audiology, 2010, Vol.49 (1), p.30-43

2010

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Newton E. Morton (1929–2018)

American journal of human genetics, 2018-06, Vol.102 (6), p.1011-1017

2018

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Deafness and retinal degeneration in a novel USH1C knock‐in mouse model

Developmental neurobiology (Hoboken, N.J.), 2010-03, Vol.70 (4), p.253-267

2010

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Modification of Depression by COMT val[superscript 158]Met Polymorphism in Children Exposed to Early Severe Psychosocial Deprivation

Child abuse & neglect, 2010-06, Vol.34 (6), p.387

2010

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Chronic and Recurrent Otitis Media: A Genome Scan for Susceptibility Loci

American journal of human genetics, 2004-12, Vol.75 (6), p.988-997

2004

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Genetic heterogeneity in Usher syndrome

American journal of medical genetics, 2004-09, Vol.130A (1), p.13-16

2004

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Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansion

Annals of neurology, 1997-05, Vol.41 (5), p.675-682

1997

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Modification of depression by COMT val158met polymorphism in children exposed to early severe psychosocial deprivation

Child abuse & neglect, 2010-06, Vol.34 (6), p.387-395

2010

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Genes and syndromic hearing loss

Journal of communication disorders, 2002-07, Vol.35 (4), p.355-366

Keats, Bronya J.B

2002

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A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

Nature genetics, 2000-09, Vol.26 (1), p.51-55

2000

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Recollections from 60 ASHG Meetings

American journal of human genetics, 2010-11, Vol.87 (5), p.580-592

2010

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Genetic variation of recent Alu insertions in human populations

Journal of molecular evolution, 1996-01, Vol.42 (1), p.22-29

1996

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Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of the USH1C gene

Genomics (San Diego, Calif.), 2004-03, Vol.83 (3), p.439-444

2004

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Mouse tales from Kresge: the deafness mouse

Journal of the American Academy of Audiology, 2003-06, Vol.14 (6), p.296-301

2003

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Modification of depression by COMT valmet polymorphism in children exposed to early severe psychosocial deprivation

Child abuse & neglect, 2010-06, Vol.34 (6), p.387-395

2010

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Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical Genetics

Genetics in medicine, 2003-07, Vol.5 (4), p.338-341

2003

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Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxia

Nucleic acids research, 2004-01, Vol.32 (19), p.5962-5971

2004

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Effects of Misspecification of Allele Frequencies on the Type I Error Rate of Model-Free Linkage Analysis

Human heredity, 2000-03, Vol.50 (2), p.126-132

2000

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Male Sexual Orientation and Genetic Evidence

Science (American Association for the Advancement of Science), 1993-12, Vol.262 (5142), p.2063-2065

1993

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A dominantly inherited progressive deafness affecting distal auditory nerve and hair cells

Journal of the Association for Research in Otolaryngology, 2004-12, Vol.5 (4), p.411-426

2004

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A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records

The role of the dopamine transporter (DAT) in the development of PTSD in preschool children

Dominant and recessive deafness caused by mutations of a novel gene, TMC1 , required for cochlear hair-cell function

Harmonin (Ush1c) is required in zebrafish Müller glial cells for photoreceptor synaptic development and function

HPPD: A newly recognized autosomal dominant disorder involving hypertelorism, preauricular sinus, punctal pits, and deafness mapping to chromosome 14q31

Multi-site diagnosis and management of 260 patients with Auditory Neuropathy/Dys-synchrony (Auditory Neuropathy Spectrum Disorder)

Newton E. Morton (1929–2018)

Deafness and retinal degeneration in a novel USH1C knock‐in mouse model

Modification of Depression by COMT val[superscript 158]Met Polymorphism in Children Exposed to Early Severe Psychosocial Deprivation

Chronic and Recurrent Otitis Media: A Genome Scan for Susceptibility Loci

Genetic heterogeneity in Usher syndrome

Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansion

Modification of depression by COMT val158met polymorphism in children exposed to early severe psychosocial deprivation

Genes and syndromic hearing loss

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

Recollections from 60 ASHG Meetings

Genetic variation of recent Alu insertions in human populations

Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of the USH1C gene

Mouse tales from Kresge: the deafness mouse

Modification of depression by COMT valmet polymorphism in children exposed to early severe psychosocial deprivation

Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical Genetics

Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxia

Effects of Misspecification of Allele Frequencies on the Type I Error Rate of Model-Free Linkage Analysis

Male Sexual Orientation and Genetic Evidence

A dominantly inherited progressive deafness affecting distal auditory nerve and hair cells

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