Works matching IS 15524841 AND DT 2014 AND VI 165B AND IP 1

Results: 11

Significant study of population stratification, sensitivity analysis and trim and fill analyses on GBA mutation and parkinson's disease.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 96, doi. 10.1002/ajmg.b.32214

By:

Liu, Jie;
Zhang, Hong‐Xin

Publication type:

Article

Genetic susceptibility for bipolar disorder and response to antidepressants in major depressive disorder.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 77, doi. 10.1002/ajmg.b.32210

By:

Tansey, Katherine E.;
Guipponi, Michel;
Domenici, Enrico;
Lewis, Glyn;
Malafosse, Alain;
O'Donovan, Michael;
Wendland, Jens R.;
Lewis, Cathryn M.;
McGuffin, Peter;
Uher, Rudolf

Publication type:

Article

Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 41, doi. 10.1002/ajmg.b.32203

By:

Kraan, Claudine M.;
Hocking, Darren R.;
Georgiou‐Karistianis, Nellie;
Metcalfe, Sylvia A.;
Archibald, Alison D.;
Fielding, Joanne;
Trollor, Julian;
Bradshaw, John L.;
Cohen, Jonathan;
Cornish, Kim M.

Publication type:

Article

How might ZNF804A variants influence risk for schizophrenia and bipolar disorder? A literature review, synthesis, and bioinformatic analysis.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 28, doi. 10.1002/ajmg.b.32207

By:

Hess, Jonathan L.;
Glatt, Stephen J.

Publication type:

Article

HLA associations in schizophrenia: Are we re-discovering the wheel?

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 19, doi. 10.1002/ajmg.b.32195

By:

Kodavali, Chowdari V.;
Watson, Annie M.;
Prasad, Konasale M.;
Celik, Cemil;
Mansour, Hader;
Yolken, Robert H.;
Nimgaonkar, Vishwajit L.

Publication type:

Article

Effects of neuregulin-1 genetic variation and depression symptom severity on longitudinal patterns of psychotic symptoms in primary care attendees.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 62, doi. 10.1002/ajmg.b.32206

By:

Bousman, C.A.;
Potiriadis, M.;
Everall, I.P.;
Gunn, J.M.

Publication type:

Article

Alterations of brain anatomy in mouse model of MDD created by replacement of homologous mouse DNA sequence with an illness-associated 6-base human CREB1 promoter sequence.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 1, doi. 10.1002/ajmg.b.32198

By:

Zubenko, George S.;
Hughes, Hugh B.;
Hitchens, T. Kevin;
Cohen, Bruce M.

Publication type:

Article

Neurophysiologic effect of GWAS derived schizophrenia and bipolar risk variants.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 9, doi. 10.1002/ajmg.b.32212

By:

Hall, Mei‐Hua;
Levy, Deborah L.;
Salisbury, Dean F.;
Haddad, Steve;
Gallagher, Patience;
Lohan, Mary;
Cohen, Bruce;
Öngür, Dost;
Smoller, Jordan W.

Publication type:

Article

Methylenetetrahydrofolate reductase ( MTHFR) genetic variation and major depressive disorder prognosis: A five-year prospective cohort study of primary care attendees.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 68, doi. 10.1002/ajmg.b.32209

By:

Bousman, Chad A.;
Potiriadis, Maria;
Everall, Ian P.;
Gunn, Jane M.

Publication type:

Article

Genome-wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 84, doi. 10.1002/ajmg.b.32211

By:

Knowles, Emma E.M.;
Carless, Melanie A.;
de Almeida, Marcio A.A.;
Curran, Joanne E.;
McKay, D. Reese;
Sprooten, Emma;
Dyer, Thomas D.;
Göring, Harald H.;
Olvera, Rene;
Fox, Peter;
Almasy, Laura;
Duggirala, Ravi;
Kent, Jack W.;
Blangero, John;
Glahn, David. C.

Publication type:

Article

Sequence analysis of 17 NRXN1 deletions.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 52, doi. 10.1002/ajmg.b.32204

By:

Hoeffding, Louise Kristine Enggaard;
Hansen, Thomas;
Ingason, Andrés;
Doung, Linh;
Thygesen, Johan H.;
Møller, Rikke S.;
Tommerup, Niels;
Kirov, George;
Rujescu, Dan;
Larsen, Lars A.;
Werge, Thomas

Publication type:

Article