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Sund, Kristen L.
39
results:
Search for persons
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Format
Online (39)
Mediatypes
Articles (Online) (25)
Bookchapter (Online) (2)
OpenAccess-fulltext (12)
Sorted by: Relevance
Sorted by: Year
?
1
P213: Exploring heterogeneity among gene lists proposed for..:
Minten, Thomas
;
Adelson, Sophia
;
Amendola, Laura
...
Genetics in Medicine Open. 2 (2024) - p. 101110 , 2024
Link:
https://doi.org/10.1016/..
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2
Long‐read sequencing and optical genome mapping identify ca..:
Sund, Kristen L.
;
Liu, Jie
;
Lee, Joyce
...
American Journal of Medical Genetics Part A. , 2024
Link:
https://doi.org/10.1002/..
?
3
P565: Optimized whole genome screening: The impact of varia..:
Sund, Kristen
;
Strom, Samuel
;
Fujita, Pauline
...
Genetics in Medicine Open. 1 (2023) 1 - p. 100612 , 2023
Link:
https://doi.org/10.1016/..
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4
eP063: Genetic variants associated with childhood cancers: ..:
Williams, Heather
;
Krysiak, Kilannin
;
Lin, Wan-Hsin
...
Genetics in Medicine. 24 (2022) 3 - p. S41-S42 , 2022
Link:
https://doi.org/10.1016/..
?
5
58. Improving the molecular diagnosis of SBDS-related disor..:
Brewer, Casey
;
Sund, Kristen
;
Wang, Xinjian
...
Cancer Genetics. 268-269 (2022) - p. 19 , 2022
Link:
https://doi.org/10.1016/..
?
6
30. Curation of genetic variants in childhood cancers withi..:
Lin, Wan-Hsin
;
Roy, Angshumoy
;
Church, Alanna
...
Cancer Genetics. 244 (2020) - p. 11-12 , 2020
Link:
https://doi.org/10.1016/..
?
7
The Genomics Research and Innovation Network: creating an i..:
Mandl, Kenneth D.
;
Glauser, Tracy
;
Krantz, Ian D.
...
Genetics in Medicine. 22 (2020) 2 - p. 371-380 , 2020
Link:
https://doi.org/10.1038/..
?
8
Correction: The Genomics Research and Innovation Network: c..:
Mandl, Kenneth D.
;
Glauser, Tracy
;
Krantz, Ian D.
...
Genetics in Medicine. 22 (2020) 2 - p. 449 , 2020
Link:
https://doi.org/10.1038/..
?
9
Confirmatory testing illustrates additional risks for struc..:
Sund, Kristen L.
;
Khattar, Divya
;
Boomer, Theresa
...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184 (2020) 2 - p. 294-301 , 2020
Link:
https://doi.org/10.1002/..
?
10
34. Curation of variants associated with pediatric tumors w..:
Raca, Gordana
;
Rao, Shruti
;
Ritter, Deborah
...
Cancer Genetics. 233-234 (2019) - p. S14 , 2019
Link:
https://doi.org/10.1016/..
?
11
Homozygous missense variant in BMPR1A resulting in BMPR sig..:
Russell, Bianca E.
;
Rigueur, Diana
;
Weaver, Kathryn N.
...
Molecular Genetics & Genomic Medicine. 7 (2019) 11 - p. , 2019
Link:
https://doi.org/10.1002/..
?
12
Using human sequencing to guide craniofacial research:
Liegel, Ryan P.
;
Finnerty, Erin
;
Blizzard, Lauren
...
genesis. 57 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1002/..
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13
39. Lessons learned from supplementary testing in constitut..:
Smolarek, Teresa A.
;
Sund, Kristen
;
Smith, Nicki
...
Cancer Genetics. 224-225 (2018) - p. 65 , 2018
Link:
https://doi.org/10.1016/..
?
14
Copb2 is essential for embryogenesis and hypomorphic mutati..:
DiStasio, Andrew
;
Driver, Ashley
;
Sund, Kristen
...
Human Molecular Genetics. 26 (2017) 24 - p. 4836-4848 , 2017
Link:
https://doi.org/10.1093/..
?
15
Mutations in SLC25A46, encoding a UGO1-like protein, cause ..:
Abrams, Alexander J
;
Hufnagel, Robert B
;
Rebelo, Adriana
...
Nature Genetics. 47 (2015) 8 - p. 926-932 , 2015
Link:
https://doi.org/10.1038/..
1-15