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Showing 201–218 of 218 results

Advanced filters: Author: D H Ledbetter Clear advanced filters

Interleukin-12 requires initial CD80-mediated T-cell activation to support immune responses toward human breast and ovarian carcinoma

Brigitte Gückel
Geeske C Meyer
Ulrich Moebius
Research01 Jun 1999
Cancer Gene Therapy

Volume: 6, P: 228-237
Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

Adam H Buchanan
Kandamurugu Manickam
Michael F Murray
ResearchOpen Access26 Oct 2017
Genetics in Medicine

Volume: 20, P: 554-558
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

A GWAS and exome-wide association study meta-analysis identifies 53 loci affecting hearing loss risk from over half a million individuals across five cohorts. Rare variants in Mendelian hearing loss genes contribute to hearing loss risk in adults.

Kavita Praveen
Lee Dobbyn
Giovanni Coppola
ResearchOpen Access03 Jun 2022
Communications Biology

Volume: 5, P: 1-12
Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

Adam H. Buchanan
Kandamurugu Manickam
Michael F. Murray
Amendments and Corrections13 Oct 2021
Genetics in Medicine

Volume: 23, P: 2470
Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes

Aimee M. Deaton
Margaret M. Parker
Paul Nioi
ResearchOpen Access03 Nov 2021
Scientific Reports

Volume: 11, P: 1-16
Postnatal Stress Produces Hyperglycemia in Adult Rats Exposed to Hypoxia-Ischemia

Ronald J McPherson
Marcella Mascher-Denen
Sandra E Juul
Research01 Sept 2009
Pediatric Research

Volume: 66, P: 278-282
A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency

Sandra Jansen
Alexander Hoischen
Bert B. A. de Vries
Research05 Dec 2017
European Journal of Human Genetics

Volume: 26, P: 54-63
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing

Christopher M Haggerty
Cynthia A James
Brandon K Fornwalt
Research04 May 2017
Genetics in Medicine

Volume: 19, P: 1245-1252
Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder

G K Chen
N Kono
R M Cantor
Research27 Sept 2005
Molecular Psychiatry

Volume: 11, P: 214-220
Sodium channels SCN1A, SCN2A and SCN3A in familial autism

L A Weiss
A Escayg
M H Meisler
Research27 Feb 2003
Molecular Psychiatry

Volume: 8, P: 186-194
Implementing genomic medicine in the clinic: the future is here

Teri A. Manolio
Rex L. Chisholm
Geoffrey S. Ginsburg
ReviewsOpen Access10 Jan 2013
Genetics in Medicine

Volume: 15, P: 258-267
QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders

A T-H Lu
J Yoon
R M Cantor
Research22 Nov 2011
Molecular Psychiatry

Volume: 18, P: 226-235
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID

B W M van Bon
B P Coe
E E Eichler
Research24 Feb 2015
Molecular Psychiatry

Volume: 21, P: 126-132
Recommendations for the integration of genomics into clinical practice

Sarah Bowdin
Adel Gilbert
Ian D. Krantz
Reviews12 May 2016
Genetics in Medicine

Volume: 18, P: 1075-1084
Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene–environment interactions

M D'Amelio
I Ricci
A M Persico
Research19 Jul 2005
Molecular Psychiatry

Volume: 10, P: 1006-1016
β₂-Adrenergic receptor gene variants and risk for autism in the AGRE cohort

K Cheslack-Postava
M D Fallin
C J Newschaffer
Research02 Jan 2007
Molecular Psychiatry

Volume: 12, P: 283-291
Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs

M Alarcón
A L Yonan
D H Geschwind
Research12 Apr 2005
Molecular Psychiatry

Volume: 10, P: 747-757
The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future

Omri Gottesman
Helena Kuivaniemi
Marc S. Williams
ReviewsOpen Access06 Jun 2013
Genetics in Medicine

Volume: 15, P: 761-771

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Interleukin-12 requires initial CD80-mediated T-cell activation to support immune responses toward human breast and ovarian carcinoma

Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes

Postnatal Stress Produces Hyperglycemia in Adult Rats Exposed to Hypoxia-Ischemia

A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency

Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing

Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder

Sodium channels SCN1A, SCN2A and SCN3A in familial autism

Implementing genomic medicine in the clinic: the future is here

QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders

Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID

Recommendations for the integration of genomics into clinical practice

Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene–environment interactions

β₂-Adrenergic receptor gene variants and risk for autism in the AGRE cohort

Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future

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