R. Sherrington

发表

Microsatellite polymorphisms for chromosome 5 bands q11.2-q13.3.

H. Gurling, D. Curtis, G. Melmer, 1993, Human heredity.

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.

G Kalsi, T Sigmundsson, D Curtis, 2001, American journal of human genetics.

NBI-921352, a first-in-class, NaV1.6 selective, sodium channel inhibitor that prevents seizures in Scn8a gain-of-function mice, and wild-type mice and rats

Angela Hussainkhel, S. Decker, Matthew Waldbrook, 2021, bioRxiv.

Identification of four novel genes contributing to familial elevated plasma HDL cholesterol in humans[S]

M. Hayden, Kenny K. Wong, L. Mitnaul, 2014, Journal of Lipid Research.

Cloning of the human dopamine D5 receptor gene and identification of a highly polymorphic microsatellite for the DRD5 locus that shows tight linkage to the chromosome 4p reference marker RAF1P1.

K. Buetow, J. Attwood, H. Gurling, 1993, Genomics.

Human Mendelian pain disorders: a key to discovery and validation of novel analgesics

M. Hayden, Y. P. Goldberg, S. Pimstone, 2012, Clinical genetics.

A linkage study of affective disorder with DNA markers for the ABO-AK1-ORM linkage group near the dopamine beta hydroxylase gene

H. Pétursson, H. Gurling, D. Curtis, 1994, Biological Psychiatry.

Molecular genetic evidence for heterogeneity in manic depression

H. Pétursson, J. Mallet, H. Gurling, 1987, Nature.

Localization of a susceptibility locus for schizophrenia on chromosome 5

Hugh Gurling, H. Pétursson, B. Barraclough, 1988, Nature.

A cosmid clone for the 5HT1A receptor (HTR1A) reveals a TaqI RFLP that shows tight linkage to dna loci D5S6, D5S39, and D5S76.

H. Gurling, D. Curtis, G. Melmer, 1991, Genomics.

Exclusion of linkage to 5qll13 in families with schizophrenia and other psychiatric disorders

H. Gurling, E. Gershon, S. Detera-Wadleigh, 1989, Nature.

Recent and future molecular genetic research into schizophrenia.

H. Pétursson, H. Gurling, D. Curtis, 1989, Schizophrenia bulletin.

Linkage disequilibrium between two highly polymorphic microsatellites.

H. Gurling, D. Curtis, H. Gurling, 1991, American journal of human genetics.

Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates.

M. Hayden, X. Breakefield, B. Brais, 2004, American journal of human genetics.

Safety and Efficacy of a Topical Sodium Channel Inhibitor (TV-45070) in Patients With Postherpetic Neuralgia (PHN)

Y. P. Goldberg, R. Malamut, S. Pimstone, 2017, The Clinical journal of pain.

Loss‐of‐function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations

M. Dubé, D. Bowsher, E. Boltshauser, 2007, Clinical genetics.

Analysis of Polymorphic Microsatellite DNA Sequences by PCR Amplification of Paraffin‐embedded Tissue: A Method of Genotyping Deceased Members of Pedigrees in Genetic Linkage Studies

H. Pétursson, H. Gurling, J. Brynjólfsson, 1991 .

Molecular genetics and heterogeneity in manic depression

H. Pétursson, M. McInnis, J. Brynjólfsson, 2008, Molecular Neurobiology.

Treatment of Nav1.7-mediated pain in inherited erythromelalgia using a novel sodium channel blocker

M. Hayden, Y. P. Goldberg, S. Pimstone, 2012, PAIN.

Linkage study of the D5 dopamine receptor gene (DRD5) in multiplex Icelandic and English schizophrenia pedigrees.

T. Sigmundsson, H. Pétursson, D. Curtis, 1996, The American journal of psychiatry.

Two microsatellite polymorphisms at the D5S39 locus.

H. Gurling, D. Curtis, G. Melmer, 1991, Nucleic acids research.

No evidence of expansion of CAG or GAA repeats in schizophrenia families and monozygotic twins

H. Pétursson, J. Vincent, M. McInnis, 1998, Human Genetics.

A linkage study with the D5 dopamine receptor in Icelandic pedigrees with multiple cases of manic depression

H. Pétursson, H. Gurling, D. Curtis, 1993 .

Regression to the mean does not exclude anticipation and unstable DNA disease.

J. Kennedy, A. Petronis, R. Sherrington, 1994, American journal of human genetics.

Genetic anticipation in schizophrenia: pro and con.

A. Paterson, J. Kennedy, A. Petronis, 1995, Clinical neuroscience.

NaV1.6 inhibition drives the efficacy of voltage-gated sodium channel inhibitors to prevent electrically induced seizures in both wild type and Scn8aN1768D/+ gain-of-function mice

Wei Zhang, Angela Hussainkhel, Matthew Waldbrook, 2023, bioRxiv.

Letter to the Editor

Y. P. Goldberg, S. Pimstone, R. Sherrington, 2014, PAIN®.