Gurling HM - Search Results

1

Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual.

Vincent JB, Herbrick JA, Gurling HM, Bolton PF, Roberts W, Scherer SW. Vincent JB, et al. Among authors: gurling hm. Am J Hum Genet. 2000 Aug;67(2):510-4. doi: 10.1086/303005. Epub 2000 Jul 7. Am J Hum Genet. 2000. PMID: 10889047 Free PMC article.

2

An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locus.

Vincent JB, Neves-Pereira ML, Paterson AD, Yamamoto E, Parikh SV, Macciardi F, Gurling HM, Potkin SG, Pato CN, Macedo A, Kovacs M, Davies M, Lieberman JA, Meltzer HY, Petronis A, Kennedy JL. Vincent JB, et al. Among authors: gurling hm. Am J Hum Genet. 2000 Mar;66(3):819-29. doi: 10.1086/302803. Am J Hum Genet. 2000. PMID: 10712198 Free PMC article.

3

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

Vincent JB, Kalsi G, Klempan T, Tatuch Y, Sherrington RP, Breschel T, McInnis MG, Brynjolfsson J, Petursson H, Gurling HM, Gottesman II, Torrey EF, Petronis A, Kennedy JL. Vincent JB, et al. Among authors: gurling hm. Hum Genet. 1998 Jul;103(1):41-7. doi: 10.1007/s004390050780. Hum Genet. 1998. PMID: 9737774

4

Genetic association analysis of serotonin system genes in bipolar affective disorder.

Vincent JB, Masellis M, Lawrence J, Choi V, Gurling HM, Parikh SV, Kennedy JL. Vincent JB, et al. Among authors: gurling hm. Am J Psychiatry. 1999 Jan;156(1):136-8. doi: 10.1176/ajp.156.1.136. Am J Psychiatry. 1999. PMID: 9892311

5

Point mutation analysis of the FMR-1 gene in autism.

Vincent JB, Konecki DS, Munstermann E, Bolton P, Poustka A, Poustka F, Gurling HM. Vincent JB, et al. Among authors: gurling hm. Mol Psychiatry. 1996 Jul;1(3):227-31. Mol Psychiatry. 1996. PMID: 9118347

6

Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes.

Gurling HM, Bolton PF, Vincent J, Melmer G, Rutter M. Gurling HM, et al. Hum Hered. 1997 Sep-Oct;47(5):254-62. doi: 10.1159/000154421. Hum Hered. 1997. PMID: 9358013

7

Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome.

Vincent JB, Gurling HM. Vincent JB, et al. Among authors: gurling hm. Hum Mutat. 1998;12(6):431-2. doi: 10.1002/(SICI)1098-1004(1998)12:6<431::AID-HUMU10>3.0.CO;2-Y. Hum Mutat. 1998. PMID: 9829913 No abstract available.

8

Oligonucleotides as short as 7-mers can be used for PCR amplification.

Vincent J, Gurling H, Melmer G. Vincent J, et al. DNA Cell Biol. 1994 Jan;13(1):75-82. doi: 10.1089/dna.1994.13.75. DNA Cell Biol. 1994. PMID: 8286042

9

Linkage between tyrosine hydroxylase gene and affective disorder cannot be excluded in two of six pedigrees.

Lim LC, Gurling H, Curtis D, Brynjolfsson J, Petursson H, Gill M. Lim LC, et al. Am J Med Genet. 1993 Dec 15;48(4):223-8. doi: 10.1002/ajmg.1320480410. Am J Med Genet. 1993. PMID: 7907843

10

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.

Gurling HM, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo BS, Read T, Murphy P, Blaveri E, McQuillin A, Petursson H, Curtis D. Gurling HM, et al. Am J Hum Genet. 2001 Mar;68(3):661-73. doi: 10.1086/318788. Am J Hum Genet. 2001. PMID: 11179014 Free PMC article.

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