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1 . Periodical
Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders
저자
by
Devanna, P
;
Chen, X S
;
Ho, J
;
Gajewski, D
;
Smith, S D
, et al.
소스
Molecular Psychiatry; May 2018, Vol. 23 Issue: 5 p1375-1384, 10p
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7 . Academic Journal
Copy number variations of chromosome 16p13.1 region associated with schizophrenia
저자
by
Ingason, A
;
Rujescu, D
;
Cichon, S
;
Sigurdsson, E
;
Sigmundsson, T
, et al.
소스
Molecular Psychiatry
. Jan 01, 2011 16(1):17-25
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7 . Academic Journal
Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts
저자
by
Muglia, P
;
Tozzi, F
;
Galwey, N W
;
Francks, C
;
Upmanyu, R
, et al.
소스
Molecular Psychiatry
. Jun 01, 2010 15(6):589-601
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7 . Academic Journal
Population-based linkage analysis of schizophrenia and bipolar case-control cohorts identifies a potential susceptibility locus on 19q13
저자
by
Francks, C
;
Tozzi, F
;
Farmer, A
;
Vincent, J B
;
Rujescu, D
, et al.
소스
Molecular Psychiatry
. Mar 01, 2010 15(3):319-325
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7 . Academic Journal
Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13.
저자
by
Ogdie, M N
;
Bakker, S C
;
Fisher, S E
;
Francks, C
;
Yang, M H
, et al.
소스
Molecular Psychiatry
. Jan2006, Vol. 11 Issue 1, p5-8. 4p. 1 Color Photograph, 1 Diagram.
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7 . Academic Journal
α-5/α-3 nicotinic receptor subunit alleles increase risk for heavy smoking
저자
by
Berrettini, W
;
Yuan, X
;
Tozzi, F
;
Song, K
;
Francks, C
, et al.
소스
Molecular Psychiatry
. Apr 01, 2008 13(4):368-373
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7 . Academic Journal
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
저자
by
Francks, C
;
Maegawa, S
;
Laurén, J
;
Abrahams, B S
;
Velayos-Baeza, A
, et al.
소스
Molecular Psychiatry
. Dec 01, 2007 12(12):1129-1139
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7 . Academic Journal
LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells
저자
by
Francks, C
;
Maegawa, S
;
Laurén, J
;
Abrahams, B S
;
Velayos-Baeza, A
, et al.
소스
Molecular Psychiatry
. Dec 01, 2007 12(12):1057-1057
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7 . Academic Journal
Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK
저자
by
Scerri, T S
;
Fisher, S E
;
Francks, C
;
MacPhie, I L
;
Paracchini, S
, et al.
소스
JOURNAL OF MEDICAL GENETICS
. Nov 01, 2004 41(11):853-857
Full Text (BMJ Journals)
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7 . Academic Journal
Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects
저자
by
Loo, S K
;
Fisher, S E
;
Francks, C
;
Ogdie, M N
;
MacPhie, I L
, et al.
소스
Molecular Psychiatry
. May 01, 2004 9(5):485-493
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