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RICHARD LIFTON, M.D.
M.D.
Internal Medicine Physician
NPI: 1689922650Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
034123(CT)
Research & Publications (20)
Rare independent mutations in renal salt handling genes contribute to blood pressure variation.
PMID 18391953·Nat Genet·2008
8-other
Salt and blood pressure: new insight from human genetic studies.
PMID 12858570·Cold Spring Harb Symp Quant Biol·2002
6-review
Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.
PMID 19289823·Proc Natl Acad Sci U S A·2009
7-preclinical
Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
PMID 19197348·PLoS Genet·2009
8-other
Angiotensin II signaling increases activity of the renal Na-Cl cotransporter through a WNK4-SPAK-dependent pathway.
PMID 19240212·Proc Natl Acad Sci U S A·2009
7-preclinical
Accelerated development of collapsing glomerulopathy in mice congenic for the HIVAN1 locus.
PMID 19092797·Kidney Int·2009
7-preclinical
Sites of regulated phosphorylation that control K-Cl cotransporter activity.
PMID 19665974·Cell·2009
7-preclinical
Susceptibility loci for murine HIV-associated nephropathy encode trans-regulators of podocyte gene expression.
PMID 19381020·J Clin Invest·2009
7-preclinical
Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population.
PMID 18322713·Neurogenetics·2008
5-case
A translocation causing increased alpha-klotho level results in hypophosphatemic rickets and hyperparathyroidism.
PMID 18308935·Proc Natl Acad Sci U S A·2008
5-case
A novel protein kinase signaling pathway essential for blood pressure regulation in humans.
PMID 18280177·Trends Endocrinol Metab·2008
6-review
Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
PMID 18272841·J Am Soc Nephrol·2008
8-other
A novel form of human mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism.
PMID 18505761·J Clin Endocrinol Metab·2008
8-other
Susceptibility loci for intracranial aneurysm in European and Japanese populations.
PMID 18997786·Nat Genet·2008
8-other
Roles of the cation-chloride cotransporters in neurological disease.
PMID 18769373·Nat Clin Pract Neurol·2008
6-review
Skint1, the prototype of a newly identified immunoglobulin superfamily gene cluster, positively selects epidermal gammadelta T cells.
PMID 18408721·Nat Genet·2008
7-preclinical
Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.
PMID 18551756·Am J Hum Genet·2008
5-case
Regulation of NKCC2 by a chloride-sensing mechanism involving the WNK3 and SPAK kinases.
PMID 18550832·Proc Natl Acad Sci U S A·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 300 CEDAR ST, TAC S341D
NEW HAVEN, CT 06519 - Phone
- (203) 737-1091
Quick Facts
- NPI
- 1689922650
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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