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Author Details
Full Name
Heather S Hain
Affiliation
Center for Applied Genomics, Children's Hospital of Philadelphia
ORCID
Career Start Year
1999
Papers
24
H Index
13
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
37120522
Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.
J Neurodev Disord
2023
34665896
Do research participants share genomic screening results with family members?
J Genet Couns
2022
35690720
An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities.
J Neurodev Disord
2022
36556166
Attitudes among Parents towards Return of Disease-Related Polygenic Risk Scores (PRS) for Their Children.
J Pers Med
2022
33479212
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders.
Transl Psychiatry
2021
33795715
JAK/STAT inhibitor therapy partially rescues the lipodystrophic autoimmune phenotype in Clec16a KO mice.
Sci Rep
2021
33927318
Inducible knockout of Clec16a in mice results in sensory neurodegeneration.
Sci Rep
2021
30774629
The Autoimmune Disorder Susceptibility Gene <i>CLEC16A</i> Restrains NK Cell Function in YTS NK Cell Line and <i>Clec16a</i> Knockout Mice.
Front Immunol
2019
30226884
CLEC16A regulates splenocyte and NK cell function in part through MEK signaling.
PLoS One
2018
27253441
The Added Value of Family Material in the Discovery of Multiple Sclerosis Genes.
Neuron
2016
27677580
Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene.
Nat Commun
2016
26244437
Effect of a Novel, Orally Active Matrix Metalloproteinase-2 and -9 Inhibitor in Spinal and Trigeminal Rat Models of Neuropathic Pain.
J Oral Facial Pain Headache
2015
24698052
Anticonvulsant activity of pregabalin in the maximal electroshock-induced seizure assay in α2δ1 (R217A) and α2δ2 (R279A) mouse mutants.
Epilepsy Res
2014
24465047
Possible therapeutic effect of trilostane in rodent models of inflammation and nociception.
Curr Ther Res Clin Exp
2013
21195549
Genomic loci and candidate genes underlying inflammatory nociception.
Pain
2011
21865767
Anti-inflammatory and immunomodulatory effects of bortezomib in various in vivo models.
Pharmacology
2011
18070349
An extensive phenotypic characterization of the hTNFalpha transgenic mice.
BMC Physiol
2007
11973013
Identification of quantitative trait loci for chemical/inflammatory nociception in mice.
Pain
2002
11420618
Quantitative trait loci influencing morphine antinociception in four mapping populations.
Mamm Genome
2001
10734168
Cocaine-induced seizure thresholds: quantitative trait loci detection and mapping in two populations derived from the C57BL/6 and DBA/2 mouse strains.
J Pharmacol Exp Ther
2000
10525057
Pharmacogenetic evidence for the involvement of 5-hydroxytryptamine (Serotonin)-1B receptors in the mediation of morphine antinociceptive sensitivity.
J Pharmacol Exp Ther
1999
10204719
Heritability of nociception I: responses of 11 inbred mouse strains on 12 measures of nociception.
Pain
1999
10204720
Heritability of nociception II. 'Types' of nociception revealed by genetic correlation analysis.
Pain
1999
1 - 24 of 24
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Oregon Health & Science University
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Frank D Mentch
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5
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Co-authored papers
3
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3
Ingrid A Holm
Harvard Medical School
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3
Patrick M A Sleiman
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Co-authored papers
3
John J Connolly
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3
Joseph T Glessner
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3
E Clayton
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
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2
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Center for Systems Neurogenetics of Addiction at The Jackson Laboratory
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2
Georgia L Wiesner
Vanderbilt Genetics Institute, Vanderbilt University Medical Center
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2
Wendy K Chung
Boston Children's Hospital, Harvard Medical School
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2
Maureen E Smith
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
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2
Iftikhar J Kullo
Mayo Clinic
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2
Christin Hoell
Northwestern University, Center for Genetic Medicine
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Cynthia A Prows
Cincinnati Children's Hospital Medical Center
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