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1 . Academic Journal
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy
저자
by
Fehlings, Darcy L.
;
Zarrei, Mehdi
;
Engchuan, Worrawat
;
Sondheimer, Neal
;
Thiruvahindrapuram, Bhooma
, et al.
소스
Nature Genetics
. 56(4):585-594
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7 . Academic Journal
70. GENE-BASED ANALYSIS OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IDENTIFIES COMMON BIOLOGICAL COMPONENTS BUT DISTINCTLY DIFFERENT GENETIC EFFECTS IN AUTISM AND SCHIZOPHRENIA
저자
by
Engchuan, Worrawat
;
Thiruvahindrapuram, Bhooma
;
MacDonald, Jeffrey R.
;
Shanta, Omar
;
Kumar, Kuldeep
, et al.
소스
In
European Neuropsychopharmacology
October 2023 75 Supplement 1:S93-S94
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7 . Academic Journal
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder.
저자
by
Chan, Ada J. S.
;
Engchuan, Worrawat
;
Reuter, Miriam S.
;
Wang, Zhuozhi
;
Thiruvahindrapuram, Bhooma
, et al.
소스
Nature Communications; 10/29/2022, Vol. 13 Issue 1, p1-16, 16p
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7 . Periodical
Rare copy number variation in posttraumatic stress disorder
저자
by
Maihofer, Adam X.
;
Engchuan, Worrawat
;
Huguet, Guillaume
;
Klein, Marieke
;
MacDonald, Jeffrey R.
, et al.
소스
Molecular Psychiatry; December 2022, Vol. 27 Issue: 12 p5062-5069, 8p
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7 . Academic Journal
The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants
저자
by
Reuter, Miriam S.
;
Walker, Susan
;
Thiruvahindrapuram, Bhooma
;
Whitney, Joe
;
Cohn, Iris
, et al.
소스
CMAJ Canadian Medical Association Journal
. Feb 05, 2018 190(5):E126-E136
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7 . Academic Journal
Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta‐analysis
저자
by
Zhang, Yanqing
;
Liu, Yi
;
Zarrei, Mehdi
;
Tong, Winnie
;
Dong, Rui
, et al.
소스
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
. Jan 01, 2018 177(1):93-100
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7 . Periodical
Association of IMMP2Ldeletions with autism spectrum disorder: A trio family study and meta‐analysis
저자
by
Zhang, Yanqing
;
Liu, Yi
;
Zarrei, Mehdi
;
Tong, Winnie
;
Dong, Rui
, et al.
소스
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics: The Official Publication of the International Society of Psychiatric Genetics; January 2018, Vol. 177 Issue: 1 p93-100, 8p
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7 . Academic Journal
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
저자
by
Lionel, Anath C.
;
Tammimies, Kristiina
;
Vaags, Andrea K.
;
Rosenfeld, Jill A.
;
Ahn, Joo Wook
, et al.
소스
Human Molecular Genetics
. May 15, 2014 23(10):2752-2768
Full Text (OUP)
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7 . Academic Journal
The Database of Genomic Variants: a curated collection of structural variation in the human genome
저자
by
MacDonald, Jeffrey R.
;
Ziman, Robert
;
Yuen, Ryan K. C.
;
Feuk, Lars
;
Scherer, Stephen W.
.
소스
Nucleic Acids Research
. Jan 01, 2014 42(D1):D986-D992
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7 . Academic Journal
A copy number variation map of the human genome.
저자
by
Zarrei, Mehdi
;
MacDonald, Jeffrey R.
;
Merico, Daniele
;
Scherer, Stephen W.
.
소스
Nature Reviews Genetics
. Mar2015, Vol. 16 Issue 3, p172-183. 12p. 1 Diagram, 1 Chart, 4 Graphs.
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