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LESLIE HOCKING, M.D.
M.D.
Psychiatry Physician
NPI: 1285712240Individual
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
34352(NC)
Research & Publications (20)
PADI4 genotype is not associated with rheumatoid arthritis in a large UK Caucasian population.
PMID 19470526·Ann Rheum Dis·2010
1-meta
Association of CD40 with rheumatoid arthritis confirmed in a large UK case-control study.
PMID 19435719·Ann Rheum Dis·2010
1-meta
A re-evaluation of three putative functional single nucleotide polymorphisms in rheumatoid arthritis.
PMID 19605748·Ann Rheum Dis·2009
1-meta
Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23.
PMID 19417005·Hum Mol Genet·2009
4-observational
Identification of AF4/FMR2 family, member 3 (AFF3) as a novel rheumatoid arthritis susceptibility locus and confirmation of two further pan-autoimmune susceptibility genes.
PMID 19359276·Hum Mol Genet·2009
4-observational
Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13.
PMID 18794857·Nat Genet·2008
4-observational
Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility.
PMID 18434327·Hum Mol Genet·2008
8-other
Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent.
PMID 17907922·J Bone Miner Res·2008
8-other
Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone.
PMID 16199218·Bone·2006
8-other
Loss of ubiquitin-binding associated with Paget's disease of bone p62 (SQSTM1) mutations.
PMID 15765181·J Bone Miner Res·2005
8-other
Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: evidence for a founder effect in patients of British descent.
PMID 15647816·J Bone Miner Res·2005
8-other
Structural and functional studies of mutations affecting the UBA domain of SQSTM1 (p62) which cause Paget's disease of bone.
PMID 15493999·Biochem Soc Trans·2004
6-review
Susceptibility to Paget's disease of bone is influenced by a common polymorphic variant of osteoprotegerin.
PMID 15312251·J Bone Miner Res·2004
8-other
Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequences.
PMID 15176995·J Bone Miner Res·2004
8-other
Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease.
PMID 12374763·Hum Mol Genet·2002
8-other
Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35.
PMID 11555792·Am J Hum Genet·2001
8-other
Mutation screening of the TNFRSF11A gene encoding receptor activator of NF kappa B (RANK) in familial and sporadic Paget's disease of bone and osteosarcoma.
PMID 11351498·Calcif Tissue Int·2001
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
- 220 SWINBURNE RD
RALEIGH, NC 27610 - Phone
- (919) 212-9566
Quick Facts
- NPI
- 1285712240
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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