I agree that this site is using cookies. You can find further informations here.
X
Jobanputra, Vaidehi
158  results:
Search for persons X
?
1

Recommendations for risk allele evidence curation, classifi..:

Schmidt, Ryan J. ; Steeves, Marcie ; Bayrak-Toydemir, Pinar...
Genetics in Medicine.  26 (2024)  3 - p. 101036 , 2024
Link: https://doi.org/10.1016/..
 
?
2

P780: Improving peripartum health is an unappreciated advan..:

Giordano, Jessica ; Pervola, Josie ; Wilson, Ashley...
Genetics in Medicine Open.  2 (2024)  - p. 101688 , 2024
Link: https://doi.org/10.1016/..
 
?
3

86 Genome sequencing as a first-tier prenatal diagnostic te..:

Jobanputra, Vaidehi ; Giordano, Jessica L. ; Pervola, Josie...
American Journal of Obstetrics and Gynecology.  230 (2024)  1 - p. S64 , 2024
Link: https://doi.org/10.1016/..
 
?
4

O44: Genome sequencing as a first-tier prenatal diagnostic ..:

Jobanputra, Vaidehi ; Giordano, Jessica ; Pervola, Josie...
Genetics in Medicine Open.  2 (2024)  - p. 101663 , 2024
Link: https://doi.org/10.1016/..
 
?
5

Reanalysis of RNA sequencing data ends diagnostic odyssey a..:

McNamee, Lucy ; Schoch, Kelly ; Huang, Alden...
American Journal of Medical Genetics Part A.  , 2024
Link: https://doi.org/10.1002/..
 
?
6

P775: Maternally inherited 11p15 duplication involving only..:

Thomas-Wilson, Amanda ; Harkavy, Nina ; Schwanke, Corbin...
Genetics in Medicine Open.  2 (2024)  - p. 101683 , 2024
Link: https://doi.org/10.1016/..
 
?
7

P765: Decoding parental reporting preferences from genome s..:

Pervola, Josie ; Tinfow, Alexandra ; Galloway, Stephanie...
Genetics in Medicine Open.  2 (2024)  - p. 101673 , 2024
Link: https://doi.org/10.1016/..
 
?
8

Advancing access to genome sequencing for rare genetic diso..:

Jobanputra, Vaidehi ; Schroeder, Brock ; Rehm, Heidi L....
npj Genomic Medicine.  9 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
?
9

Clinical Impact of Telomere Length Testing for Interstitial..:

Zhang, David ; Eckhardt, Christina M. ; McGroder, Claire...
CHEST.  , 2024
Link: https://doi.org/10.1016/..
 
?
10

P764: RNA sequencing improves assessment of variants of unc..:

Rehman, Atteeq ; Thomas-Wilson, Amanda ; Mau-Them, Frederic Tran...
Genetics in Medicine Open.  2 (2024)  - p. 101672 , 2024
Link: https://doi.org/10.1016/..
 
?
11

Evidence review and considerations for use of first line ge..:

Wigby, Kristen M. ; Brockman, Deanna ; Costain, Gregory...
npj Genomic Medicine.  9 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
?
12

Spliceosome malfunction causes neurodevelopmental disorders..:

Li, Dong ; Wang, Qin ; Bayat, Allan...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10760965/.  , 2024
Link: http://www.ncbi.nlm.nih...
 
?
13

Identification of copy number variants with genome sequenci..:

Bonini, Katherine E. ; Thomas‐Wilson, Amanda ; Marathe, Priya N....
Clinical Genetics.  104 (2023)  2 - p. 210-225 , 2023
Link: https://doi.org/10.1111/..
 
?
14

The best of both worlds: Blending cutting‐edge research wit..:

Sullivan, Jennifer A. ; Spillmann, Rebecca C. ; Schoch, Kelly...
Clinical Genetics.  105 (2023)  1 - p. 62-71 , 2023
Link: https://doi.org/10.1111/..
 
?
15

Genetic insights into childhood-onset schizophrenia: The yi..:

Alkelai, Anna ; Greenbaum, Lior ; Shohat, Shahar...
Schizophrenia Research.  252 (2023)  - p. 138-145 , 2023
Link: https://doi.org/10.1016/..
 
1-15