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Kelley, Whitley
100
results:
Search for persons
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Format
Online (99)
Print (1)
Mediatypes
Books (1)
E-Books (1)
Articles (Online) (62)
OpenAccess-fulltext (36)
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?
1
P508: Medically-actionable disease risk variants in a diver..:
Kelley, Whitley
;
Moss, Irene
;
Asif, Irfan
...
Genetics in Medicine Open. 2 (2024) - p. 101407 , 2024
Link:
https://doi.org/10.1016/..
?
2
Information-seeking preferences in diverse patients receivi..:
Slavotinek, Anne
;
Prasad, Hannah
;
Outram, Simon
...
Genetics in Medicine. 25 (2023) 9 - p. 100899 , 2023
Link:
https://doi.org/10.1016/..
?
3
Does genetic testing offer utility as a supplement to tradi..:
May, Thomas
;
Smith, Crystal L
;
Kelley, Whitley
...
Family Practice. 40 (2023) 5-6 - p. 760-767 , 2023
Link:
https://doi.org/10.1093/..
?
4
P392: Genomic medicine and primary care: The Alabama Genomi..:
Kelley, Whitley
;
East, Kelly
;
Asif, Irfan
...
Genetics in Medicine Open. 1 (2023) 1 - p. 100428 , 2023
Link:
https://doi.org/10.1016/..
?
5
eP494: Integration of genomics into primary care via the Al..:
Korf, Bruce
;
Absher, Devin
;
Asif, Irfan
...
Genetics in Medicine. 24 (2022) 3 - p. S314-S315 , 2022
Link:
https://doi.org/10.1016/..
?
6
A study of elective genome sequencing and pharmacogenetic t..:
Cochran, Meagan
;
East, Kelly
;
Greve, Veronica
...
Molecular Genetics & Genomic Medicine. 9 (2021) 9 - p. , 2021
Link:
https://doi.org/10.1002/..
?
7
Relief, empowerment, and uncertainty: Perspectives of clini..:
Greve, Veronica
;
Odom, Katherine
;
Pudner, Susanna
...
Molecular Genetics and Metabolism. 132 (2021) - p. S44-S45 , 2021
Link:
https://doi.org/10.1016/..
?
8
SYT1-associated neurodevelopmental disorder: a case series:
Baker, Kate
;
Gordon, Sarah L
;
Melland, Holly
...
Brain. 141 (2018) 9 - p. 2576-2591 , 2018
Link:
https://doi.org/10.1093/..
?
9
Errors in Genome Sequencing Result Disclosures: A Randomize..:
Coleman, Tanner F.
;
Pugh, Jada
;
Kelley, Whitley V.
...
Genetics in Medicine. , 2024
Link:
https://doi.org/10.1016/..
?
10
Poison exon annotations improve the yield of clinically rel..:
Felker, Stephanie A.
;
Lawlor, James M.J.
;
Hiatt, Susan M.
...
Genetics in Medicine. 25 (2023) 8 - p. 100884 , 2023
Link:
https://doi.org/10.1016/..
?
11
338 The Alabama Genomic Health Initiative: Integrating Geno..:
Limdi, Nita A
;
Absher, Devin
;
Asif, Irf
...
Journal of Clinical and Translational Science. 7 (2023) s1 - p. 100-101 , 2023
Link:
https://doi.org/10.1017/..
?
12
Missense variants in RPH3A cause defects in excitatory syna..:
Pavinato, Lisa
;
Stanic, Jennifer
;
Barzasi, Marta
...
Genetics in Medicine. 25 (2023) 11 - p. 100922 , 2023
Link:
https://doi.org/10.1016/..
?
13
Parents' Perspectives on the Utility of Genomic Sequencing ..:
Lemke, Amy A.
;
Thompson, Michelle L.
;
Gimpel, Emily C.
...
Journal of Personalized Medicine. 13 (2023) 7 - p. 1026 , 2023
Link:
https://doi.org/10.3390/..
?
14
De novo variants in CNOT9 cause a neurodevelopmental disord..:
von Wintzingerode, Lydia
;
Ben-Zeev, Bruria
;
Cesario, Claudia
...
Genetics in Medicine. 25 (2023) 7 - p. 100859 , 2023
Link:
https://doi.org/10.1016/..
?
15
Medical and psychosocial outcomes of state‐funded populatio..:
Cannon, Ashley
;
McMillan, Olivia
;
Kelley, Whitley V.
...
Clinical Genetics. 104 (2023) 4 - p. 434-442 , 2023
Link:
https://doi.org/10.1111/..
1-15
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