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Guo, Shengru
187
results:
Search for persons
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Online (187)
Mediatypes
Articles (Online) (94)
Bookchapter (Online) (2)
OpenAccess-fulltext (91)
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1
Genetic heterogeneity in hereditary hearing loss: Potential..:
Ramzan, Memoona
;
Zafeer, Mohammad Faraz
;
Abad, Clemer
...
European Journal of Human Genetics. 32 (2024) 6 - p. 639-646 , 2024
Link:
https://doi.org/10.1038/..
?
2
Identification of novel MYH14 variants in families with aut..:
Duman, Duygu
;
Ramzan, Memoona
;
Subasioglu, Asli
...
American Journal of Medical Genetics Part A. 194 (2024) 6 - p. , 2024
Link:
https://doi.org/10.1002/..
?
3
P121: Comparison of diagnostic outcome amongst different et..:
Bivona, Stephanie
;
Tekin, Mustafa
;
Bademci, Guney
...
Genetics in Medicine Open. 1 (2023) 1 - p. 100150 , 2023
Link:
https://doi.org/10.1016/..
?
4
Genome sequencing identifies coding and non-coding variants..:
Ramzan, Memoona
;
Duman, Duygu
;
Hendricks, LeShon Chere Peart
...
Journal of Human Genetics. 68 (2023) 10 - p. 657-669 , 2023
Link:
https://doi.org/10.1038/..
?
5
H4C5 missense variant leads to a neurodevelopmental phenoty..:
Borja, Nicholas
;
Borjas‐Mendoza, Paulo
;
Bivona, Stephanie
...
American Journal of Medical Genetics Part A. 191 (2023) 7 - p. 1911-1916 , 2023
Link:
https://doi.org/10.1002/..
?
6
Genome‐wide identification of modifiers of age‐at‐onset for..:
Nuytemans, Karen
;
Guo, Shengru
;
La, Jong Ok
...
Alzheimer's & Dementia. 19 (2023) S12 - p. , 2023
Link:
https://doi.org/10.1002/..
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7
P642: Diagnostic yield of multi-omics approach in Undiagnos..:
Bademci, Guney
;
Bivona, Stephanie
;
Peart, LeShon
...
Genetics in Medicine Open. 1 (2023) 1 - p. 100707 , 2023
Link:
https://doi.org/10.1016/..
?
8
Modeling gene expression on the X chromosome in the brain f..:
Zhang, Xueyi
;
Guo, Shengru
;
Naj, Adam C.
...
Alzheimer's & Dementia. 18 (2022) S4 - p. , 2022
Link:
https://doi.org/10.1002/..
?
9
Genome sequencing reveals novel noncoding variants in PLA2G..:
Borja, Nicholas
;
Bivona, Stephanie
;
Peart, Lé Shon
...
Molecular Genetics & Genomic Medicine. 10 (2022) 4 - p. , 2022
Link:
https://doi.org/10.1002/..
?
10
Mutations inMINAR2encoding membrane integral NOTCH2-associa..:
Bademci, Guney
;
Lachgar-Ruiz, María
;
Deokar, Mangesh
...
Proceedings of the National Academy of Sciences. 119 (2022) 26 - p. , 2022
Link:
https://doi.org/10.1073/..
?
11
Response to Comment on "Large-scale GWAS reveals insights i..:
Ganna, Andrea
;
Verweij, Karin J. H.
;
Nivard, Michel G.
...
Science. 371 (2021) 6536 - p. , 2021
Link:
https://doi.org/10.1126/..
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12
Genome-Wide Linkage and Association Study of Childhood Gend..:
Sanders, Alan R.
;
Beecham, Gary W.
;
Guo, Shengru
...
Archives of Sexual Behavior. 50 (2021) 8 - p. 3377-3383 , 2021
Link:
https://doi.org/10.1007/..
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13
Author Correction: Genomic evidence consistent with antagon..:
Zietsch, Brendan P.
;
Sidari, Morgan J.
;
Abdellaoui, Abdel
...
Nature Human Behaviour. 5 (2021) 9 - p. 1259-1259 , 2021
Link:
https://doi.org/10.1038/..
?
14
Genome-Wide Linkage Study Meta-Analysis of Male Sexual Orie..:
Sanders, Alan R.
;
Beecham, Gary W.
;
Guo, Shengru
...
Archives of Sexual Behavior. 50 (2021) 8 - p. 3371-3375 , 2021
Link:
https://doi.org/10.1007/..
?
15
Genomic evidence consistent with antagonistic pleiotropy ma..:
Zietsch, Brendan P.
;
Sidari, Morgan J.
;
Abdellaoui, Abdel
...
Nature Human Behaviour. 5 (2021) 9 - p. 1251-1258 , 2021
Link:
https://doi.org/10.1038/..
1-15