E-LIB Suche - Ergebnisse für: MacDonald, Jeffrey R

1

Comprehensive whole-genome sequence analyses provide insigh..:

Fehlings, Darcy L. ; Zarrei, Mehdi ; Engchuan, Worrawat...
Nature Genetics. 56 (2024) 4 - p. 585-594 , 2024

2

70. GENE-BASED ANALYSIS OF RARE CNVS ACROSS SIX PSYCHIATRIC..:

Engchuan, Worrawat ; Thiruvahindrapuram, Bhooma ; MacDonald, Jeffrey R....
European Neuropsychopharmacology. 75 (2023) - p. S93-S94 , 2023

Link: https://doi.org/10.1016/..

3

Gene copy number variation and pediatric mental health/neur..:

Zarrei, Mehdi ; Burton, Christie L ; Engchuan, Worrawat...
Human Molecular Genetics. 32 (2023) 15 - p. 2411-2421 , 2023

Link: https://doi.org/10.1093/..

4

Genomic architecture of autism from comprehensive whole-gen..:

Trost, Brett ; Thiruvahindrapuram, Bhooma ; Chan, Ada J.S....
Cell. 185 (2022) 23 - p. 4409-4427.e18 , 2022

Link: https://doi.org/10.1016/..

5

Genome-wide rare variant score associates with morphologica..:

Chan, Ada J. S. ; Engchuan, Worrawat ; Reuter, Miriam S....
Nature Communications. 13 (2022) 1 - p. , 2022

Link: https://doi.org/10.1038/..

6

Rare copy number variation in posttraumatic stress disorder:

Maihofer, Adam X. ; Engchuan, Worrawat ; Huguet, Guillaume...
Molecular Psychiatry. 27 (2022) 12 - p. 5062-5069 , 2022

Link: https://doi.org/10.1038/..

7

A large data resource of genomic copy number variation acro..:

Zarrei, Mehdi ; Burton, Christie L. ; Engchuan, Worrawat...
npj Genomic Medicine. 4 (2019) 1 - p. , 2019

Link: https://doi.org/10.1038/..

8

De novo and rare inherited copy-number variations in the he..:

Zarrei, Mehdi ; Fehlings, Darcy L. ; Mawjee, Karizma...
Genetics in Medicine. 20 (2018) 2 - p. 172-180 , 2018

Link: https://doi.org/10.1038/..

9

Association of IMMP2L deletions with autism spectrum disord..:

Zhang, Yanqing ; Liu, Yi ; Zarrei, Mehdi...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 177 (2017) 1 - p. 93-100 , 2017

Link: https://doi.org/10.1002/..

10

Whole genome sequencing resource identifies 18 new candidat..:

C Yuen, Ryan K ; Merico, Daniele ; Bookman, Matt...
Nature Neuroscience. 20 (2017) 4 - p. 602-611 , 2017

Link: https://doi.org/10.1038/..

11

Genome-wide characteristics of de novo mutations in autism:

Yuen, Ryan KC ; Merico, Daniele ; Cao, Hongzhi...
npj Genomic Medicine. 1 (2016) 1 - p. , 2016

Link: https://doi.org/10.1038/..

12

A high-resolution copy-number variation resource for clinic..:

Uddin, Mohammed ; Thiruvahindrapuram, Bhooma ; Walker, Susan...
Genetics in Medicine. 17 (2015) 9 - p. 747-752 , 2015

Link: https://doi.org/10.1038/..

13

Development of a high-resolution Y-chromosome microarray fo..:

Yuen, Ryan K.C. ; Merkoulovitch, Anna ; MacDonald, Jeffrey R....
Fertility and Sterility. 101 (2014) 4 - p. 1079-1085.e3 , 2014

Link: https://doi.org/10.1016/..

14

The Database of Genomic Variants: a curated collection of s..:

MacDonald, Jeffrey R. ; Ziman, Robert ; Yuen, Ryan K. C...
Nucleic Acids Research. 42 (2013) D1 - p. D986-D992 , 2013

Link: https://doi.org/10.1093/..

15

Mechanisms of Formation of Structural Variation in a Fully ..:

Pang, Andy Wing Chun ; Migita, Ohsuke ; MacDonald, Jeffrey R...
Human Mutation. 34 (2012) 2 - p. 345-354 , 2012

Link: https://doi.org/10.1002/..