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Satterstrom, F Kyle
105
results:
Format
Online (105)
Mediatypes
Articles (Online) (44)
OpenAccess-fulltext (61)
Sorted by: Relevance
Sorted by: Year
?
1
T63. CROSS-DISORDER ANALYSIS OF AUTISM AND ADHD USING RARE ..:
Duan, Jinjie
;
Grove, Jakob
;
Demontis, Ditte
...
European Neuropsychopharmacology. 75 (2023) - p. S195-S196 , 2023
Link:
https://doi.org/10.1016/..
?
2
Genome-wide analyses of ADHD identify 27 risk loci, refine ..:
Demontis, Ditte
;
Walters, G. Bragi
;
Athanasiadis, Georgios
...
Nature Genetics. 55 (2023) 2 - p. 198-208 , 2023
Link:
https://doi.org/10.1038/..
?
3
Landscape of mSWI/SNF chromatin remodeling complex perturba..:
Valencia, Alfredo M.
;
Sankar, Akshay
;
van der Sluijs, Pleuntje J.
...
Nature Genetics. 55 (2023) 8 - p. 1400-1412 , 2023
Link:
https://doi.org/10.1038/..
?
4
Author Correction: Genome-wide analyses of ADHD identify 27..:
Demontis, Ditte
;
Walters, G. Bragi
;
Athanasiadis, Georgios
...
Nature Genetics. 55 (2023) 4 - p. 730-730 , 2023
Link:
https://doi.org/10.1038/..
?
5
ANALYSIS OF RARE CODING AND COMMON VARIANTS IN AUTISM AND C..:
Duan, Jinjie
;
Grove, Jakob
;
Satterstrom, F. Kyle
...
European Neuropsychopharmacology. 63 (2022) - p. e19-e20 , 2022
Link:
https://doi.org/10.1016/..
?
6
The female protective effect against autism spectrum disord..:
Wigdor, Emilie M.
;
Weiner, Daniel J.
;
Grove, Jakob
...
Cell Genomics. 2 (2022) 6 - p. 100134 , 2022
Link:
https://doi.org/10.1016/..
?
7
Differences in the genetic architecture of common and rare ..:
Rajagopal, Veera M.
;
Duan, Jinjie
;
Vilar-Ribó, Laura
...
Nature Genetics. 54 (2022) 8 - p. 1117-1124 , 2022
Link:
https://doi.org/10.1038/..
?
8
Rare coding variation provides insight into the genetic arc..:
Fu, Jack M.
;
Satterstrom, F. Kyle
;
Peng, Minshi
...
Nature Genetics. 54 (2022) 9 - p. 1320-1331 , 2022
Link:
https://doi.org/10.1038/..
?
9
Author Correction: Transcript expression-aware annotation i..:
Genome Aggregation Database Production Team
;
Cummings, Beryl B.
;
Karczewski, Konrad J.
...
Nature. 590 (2021) 7846 - p. E54-E54 , 2021
Link:
https://doi.org/10.1038/..
?
10
47. GENE DISCOVERY FROM EXOME SEQUENCING IN AUTISM AND COMP..:
Satterstrom, F. Kyle
;
Fu, Jack
;
Peng, Minshi
...
European Neuropsychopharmacology. 51 (2021) - p. e65-e66 , 2021
Link:
https://doi.org/10.1016/..
?
11
Prevalence and phenotypic impact of rare potentially damagi..:
Mahjani, Behrang
;
De Rubeis, Silvia
;
Gustavsson Mahjani, Christina
...
Molecular Autism. 12 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
12
Large-Scale Exome Sequencing Study Implicates Both Developm..:
Satterstrom, F. Kyle
;
Kosmicki, Jack A.
;
Wang, Jiebiao
...
Cell. 180 (2020) 3 - p. 568-584.e23 , 2020
Link:
https://doi.org/10.1016/..
?
13
Transcript expression-aware annotation improves rare varian..:
Cummings, Beryl B.
;
Karczewski, Konrad J.
;
Kosmicki, Jack A.
...
Nature. 581 (2020) 7809 - p. 452-458 , 2020
Link:
https://doi.org/10.1038/..
?
14
Autism spectrum disorder and attention deficit hyperactivit..:
iPSYCH-Broad Consortium
;
Satterstrom, F. Kyle
;
Walters, Raymond K.
...
Nature Neuroscience. 22 (2019) 12 - p. 1961-1965 , 2019
Link:
https://doi.org/10.1038/..
?
15
68THE ROLE OF DELETERIOUS ULTRA-RARE VARIANTS IN ADHD RISK:
Demontis, Ditte
;
Satterstrom, F. Kyle
;
Duan, Jinjie
...
European Neuropsychopharmacology. 29 (2019) - p. S1106 , 2019
Link:
https://doi.org/10.1016/..
1-15