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Brand*, Harrison
244
results:
Search for persons
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Format
Online (244)
Mediatypes
E-Books (1)
Articles (Online) (80)
Bookchapter (Online) (1)
OpenAccess-fulltext (162)
Sorted by: Relevance
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?
1
Narrowing the diagnostic gap: Genomes, episignatures, long-..:
Dias, Kerith-Rae
;
Shrestha, Rupendra
;
Schofield, Deborah
...
Genetics in Medicine. 26 (2024) 5 - p. 101076 , 2024
Link:
https://doi.org/10.1016/..
?
2
O11: An atlas of 1.2M structural variants across global pop..:
Brand, Harrison
;
Zhao, Xuefang
;
Fu, Jack
...
Genetics in Medicine Open. 2 (2024) - p. 101015 , 2024
Link:
https://doi.org/10.1016/..
?
3
P575: The Rare Genomes Project: Improving access to genomic..:
Austin-Tse, Christina
;
DiTroia, Stephanie
;
O'Leary, Melanie
...
Genetics in Medicine Open. 2 (2024) - p. 101481 , 2024
Link:
https://doi.org/10.1016/..
?
4
Author Correction: GATK-gCNV enables the discovery of rare ..:
Babadi, Mehrtash
;
Fu, Jack M.
;
Lee, Samuel K.
...
Nature Genetics. 56 (2024) 3 - p. 553-553 , 2024
Link:
https://doi.org/10.1038/..
?
5
Improving prenatal diagnosis through standards and aggregat..:
Duyzend, Michael H.
;
Cacheiro, Pilar
;
Jacobsen, Julius O. B.
...
Prenatal Diagnosis. 44 (2024) 4 - p. 454-464 , 2024
Link:
https://doi.org/10.1002/..
?
6
A harmonized public resource of deeply sequenced diverse hu..:
Koenig, Zan
;
Yohannes, Mary T.
;
Nkambule, Lethukuthula L.
...
Genome Research. , 2024
Link:
https://doi.org/10.1101/..
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7
Rare variants found in clinical gene panels illuminate the ..:
Diaz Perez, Kimberly K.
;
Curtis, Sarah W.
;
Sanchis-Juan, Alba
...
Genetics in Medicine. 25 (2023) 10 - p. 100918 , 2023
Link:
https://doi.org/10.1016/..
?
8
Genomic autopsy to identify underlying causes of pregnancy ..:
Byrne, Alicia B.
;
Arts, Peer
;
Ha, Thuong T.
...
Nature Medicine. 29 (2023) 1 - p. 180-189 , 2023
Link:
https://doi.org/10.1038/..
?
9
Genome-wide structural variant analysis identifies risk loc..:
Kaivola, Karri
;
Chia, Ruth
;
Ding, Jinhui
...
Cell Genomics. 3 (2023) 6 - p. 100316 , 2023
Link:
https://doi.org/10.1016/..
?
10
Author Correction: Genomic autopsy to identify underlying c..:
Byrne, Alicia B.
;
Arts, Peer
;
Ha, Thuong T.
...
Nature Medicine. 30 (2023) 1 - p. 302-302 , 2023
Link:
https://doi.org/10.1038/..
?
11
Trio-based GWAS identifies novel associations and subtype-s..:
Robinson, Kelsey
;
Mosley, Trenell J.
;
Rivera-González, Kenneth S.
...
Human Genetics and Genomics Advances. 4 (2023) 4 - p. 100234 , 2023
Link:
https://doi.org/10.1016/..
?
12
PLS3 missense variants affecting the actin-binding domains ..:
Petit, Florence
;
Longoni, Mauro
;
Wells, Julie
...
The American Journal of Human Genetics. 110 (2023) 10 - p. 1787-1803 , 2023
Link:
https://doi.org/10.1016/..
?
13
Structural variants in Lewy body dementia and frontotempora..:
Kaivola, Karri
;
Chia, Ruth
;
Ding, Jinhui
...
Alzheimer's & Dementia. 19 (2023) S12 - p. , 2023
Link:
https://doi.org/10.1002/..
?
14
Phenotype and genetic analysis of data collected within the..:
Kipkemoi, Patricia
;
Kim, Heesu Ally
;
Christ, Bjorn
...
Neuron. 111 (2023) 18 - p. 2800-2810.e5 , 2023
Link:
https://doi.org/10.1016/..
?
15
O39: Comprehensive, high-resolution, and non-invasive prena..:
Duyzend, Michael
;
Brand, Harrison
;
Whelan, Christopher
...
Genetics in Medicine Open. 1 (2023) 1 - p. 100646 , 2023
Link:
https://doi.org/10.1016/..
1-15