E-LIB Suche - Ergebnisse für: Sleiman, Patrick M. A

1

Biliary atresia is associated with polygenic susceptibility..:

Glessner, Joseph T. ; Ningappa, Mylarappa B. ; Ngo, Kim A....
Journal of Hepatology. 79 (2023) 6 - p. 1385-1395 , 2023

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

2

Trans‐ethnic genomic informed risk assessment for Alzheimer..:

Sleiman, Patrick M. ; Qu, Hui‐Qi ; Connolly, John J....
Alzheimer's & Dementia. 19 (2023) 12 - p. 5765-5772 , 2023

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

3

Rare recurrent copy number variations in metabotropic gluta..:

Glessner, Joseph T. ; Khan, Munir E. ; Chang, Xiao...
Journal of Neurodevelopmental Disorders. 15 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

4

Trans‐ethnic polygenic risk scores for body mass index: An ..:

Qu, Hui‐Qi ; Connolly, John J ; Kraft, Peter...
Clinical and Translational Medicine. 13 (2023) 6 - p. , 2023

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

5

Functional characterization of all missense variants in LEP..:

Shah, Bhavik P. ; Sleiman, Patrick M. ; Mc Donald, Jessica..
Expert Review of Endocrinology & Metabolism. 18 (2023) 2 - p. 209-219 , 2023

Link: https://doi.org/10.1080/..

6

European and multi-ancestry genome-wide association meta-an..:

Budu-Aggrey, Ashley ; Kilanowski, Anna ; Sobczyk, Maria K....
Nature Communications. 14 (2023) 1 - p. , 2023

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

7

Identification of novel loci in obstructive sleep apnea in ..:

Quinlan, Courtney M ; Chang, Xiao ; March, Michael...
SLEEP. 47 (2022) 3 - p. , 2022

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

8

An electronic health record (EHR) phenotype algorithm to id..:

Slaby, Isabella ; Hain, Heather S. ; Abrams, Debra...
Journal of Neurodevelopmental Disorders. 14 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

9

Expansion of Schizophrenia Gene Network Knowledge Using Mac..:

Liu, Yichuan ; Qu, Hui-Qi ; Chang, Xiao...
Frontiers in Psychiatry. 13 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

10

Mutation burden analysis of six common mental disorders in ..:

Liu, Yichuan ; Qu, Hui-Qi ; Chang, Xiao...
Human Molecular Genetics. 31 (2022) 22 - p. 3769-3776 , 2022

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

11

Saudi Arabian CML patient with a novel four‐way translocati..:

Dridi, Walid ; Kanfar, Solaf ; Sleiman, Patrick M. A....
Molecular Genetics & Genomic Medicine. 10 (2022) 6 - p. , 2022

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

12

Identification of Novel Loci Shared by Juvenile Idiopathic ..:

Li, Jin ; Li, Yun R. ; Glessner, Joseph T....
Arthritis & Rheumatology. 74 (2022) 8 - p. 1420-1429 , 2022

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

13

Genome-wide association study in minority children with ast..:

Joo, Jaehyun ; Mak, Angel C. Y. ; Xiao, Shujie...
Scientific Reports. 12 (2022) 1 - p. , 2022

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

14

ParseCNV2: efficient sequencing tool for copy number variat..:

Glessner, Joseph T. ; Li, Jin ; Liu, Yichuan...
European Journal of Human Genetics. 31 (2022) 3 - p. 304-312 , 2022

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

15

Burden of rare coding variants reveals genetic heterogeneit..:

Liu, Yichuan ; Qu, Hui-Qi ; Qu, Jingchun...
Respiratory Research. 23 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..