Nanda A. Singh

发表

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy

J. Lupski, M. Leppert, J. Nathans, 1997, Nature Genetics.

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

Robin J. Leach, Mark Leppert, Carole Charlier, 1998, Nature Genetics.

Mutation of the Stargardt Disease Gene (ABCR) in Age-Related Macular Degeneration

Paul S. Bernstein, Richard A. Lewis, Amy Hutchinson, 1997 .

Association of adipose and red blood cell lipids with severity of dominant Stargardt macular dystrophy (STGD3) secondary to an ELOVL4 mutation.

M. Leppert, P. Bernstein, Nanda A. Singh, 2004, Archives of ophthalmology.

A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome

M. Leppert, M. Dixon, A. Peiffer, 2009, PLoS genetics.

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

Mark Leppert, Carole Charlier, Roberta Melis, 1998, Nature Genetics.

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.

M. Leppert, V. Anderson, M. Sanguinetti, 2003, Brain : a journal of neurology.

Nonsyndromic seizure disorders: epilepsy and the use of the internet to advance research.

M. Leppert, Nanda A. Singh, Mark F Leppert, 2003, Annual review of genomics and human genetics.

A Candidate Gene Approach Identifies the CHRNA5-A3-B4 Region as a Risk Factor for Age-Dependent Nicotine Addiction

Megan E. Piper, W. McMahon, H. Coon, 2008, PLoS genetics.

Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypes.

Megan E. Piper, W. McMahon, H. Coon, 2009, Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco.

Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization

M. Leppert, K. Wilcox, J. Noebels, 2008, The Journal of physiology.

The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial

J. Lupski, M. Leppert, R. Lewis, 1999, Vision Research.

Genotype-phenotype analysis of ABCR variants in macular degeneration probands and siblings.

J. Lupski, M. Leppert, R. Lewis, 2002, Investigative ophthalmology & visual science.

TXNIP gene not associated with familial combined hyperlipidemia in the NHLBI Family Heart Study.

H. Coon, M. Leppert, M. Province, 2004, Atherosclerosis.

Responses of Limbic and Extrapyramidal Neurotensin Systems to Stimulants of Abuse

G. Hanson, J. Gibb, K. Merchant, 1992, Annals of the New York Academy of Sciences.

Role of N-methyl-d-aspartate receptors in dopamine D1-, but not D2-, mediated changes in striatal and accumbens neurotensin systems

G. Hanson, J. Gibb, Nanda A. Singh, 1992, Brain Research.

Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions

K. Wilcox, C. Pappas, Nanda A. Singh, 2009, Epilepsia.

Susceptibility Genes in Human Epilepsy

M. Leppert, M. Leppert, Nanda A. Singh, 1999, Seminars in neurology.

Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration.

J. Lupski, M. Leppert, A. Peiffer, 1997, Science.

Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease.

J. Lupski, M. Leppert, A. Hutchinson, 1999, American journal of human genetics.

Mouse Models of Benign Familial Neonatal Convulsions (BFNC): Mutations in KCNQ (Kv7) Genes

M. Leppert, K. Wilcox, H. White, 2009 .

Corrigendum: A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

J. Lupski, J. Nathans, A. Peiffer, 1997, Nature Genetics.

A Candidate Gene Approach Identifies the CHRNA5-A3-B4 Region as a Risk Factor for Age-Dependent Nicotine Addiction

W. McMahon, H. Coon, M. Leppert, 2008, PLoS Genetics.

Dynamic dopaminergic regulation of neuropeptide Y systems in discrete striatal and accumbens regions.

G. Hanson, J. Gibb, Nanda A. Singh, 1994, European journal of pharmacology.

Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions

K. Wilcox, C. Pappas, Nanda A. Singh, 2009, Epilepsia.