Back to Search
JERRY TERWILLIGER, MD
MD
Pediatrics Physician
NPI: 1598730376Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
144861-1(NY)MD028322E(PA)
Research & Publications (20)
An association analysis of murine anxiety genes in humans implicates novel candidate genes for anxiety disorders.
PMID 18639233·Biol Psychiatry·2008
7-preclinical
An utter refutation of the "fundamental theorem of the HapMap".
PMID 16479260·Eur J Hum Genet·2006
8-other
Confounding, ascertainment bias, and the blind quest for a genetic 'fountain of youth'.
PMID 14649335·Ann Med·2003
6-review
A bias-ed assessment of the use of SNPs in human complex traits.
PMID 12433588·Curr Opin Genet Dev·2002
6-review
On the resolution and feasibility of genome scanning approaches.
PMID 11037331·Adv Genet·2001
6-review
Gene mapping in the 20th and 21st centuries: statistical methods, data analysis, and experimental design.
PMID 10721614·Hum Biol·2000
6-review
A likelihood-based extended admixture model of oligogenic inheritance in 'model-based' and 'model-free' analysis.
PMID 10878659·Eur J Hum Genet·2000
8-other
Linkage analysis of schizophrenia controlling for population substructure.
PMID 19086037·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
Candidate endophenotypes for genetic studies of suicidal behavior.
PMID 19201395·Biol Psychiatry·2009
8-other
ForSim: a tool for exploring the genetic architecture of complex traits with controlled truth.
PMID 18565989·Bioinformatics·2008
8-other
Consistently replicating locus linked to migraine on 10q22-q23.
PMID 18423523·Am J Hum Genet·2008
8-other
Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans.
PMID 17701907·Am J Hum Genet·2007
8-other
Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.
PMID 17185386·Hum Mol Genet·2007
8-other
Trait components provide tools to dissect the genetic susceptibility of migraine.
PMID 16773568·Am J Hum Genet·2006
8-other
Testing of variants of the MTHFR and ESR1 genes in 1798 Finnish individuals fails to confirm the association with migraine with aura.
PMID 17116097·Cephalalgia·2006
8-other
Prostatic intraepithelial neoplasia and adenocarcinoma in mice expressing a probasin-Neu oncogenic transgene.
PMID 16401639·Carcinogenesis·2006
7-preclinical
AUTOGSCAN: powerful tools for automated genome-wide linkage and linkage disequilibrium analysis.
PMID 15836805·Twin Res Hum Genet·2005
8-other
Integrative annotation of 21,037 human genes validated by full-length cDNA clones.
PMID 15103394·PLoS Biol·2004
8-other
The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories.
PMID 12490532·Hum Mol Genet·2003
8-other
A genomewide screen of 345 families for autism-susceptibility loci.
PMID 13680528·Am J Hum Genet·2003
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1 GUTHRIE SQ
SAYRE, PA 18840 - Phone
- (570) 887-3070
Quick Facts
- NPI
- 1598730376
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile