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Bhola, Priya T
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1

Identification of a DNA methylation episignature for recurr..:

Haghshenas, Sadegheh ; Karimi, Karim ; Stevenson, Roger E....
The American Journal of Human Genetics.  111 (2024)  8 - p. 1643-1655 , 2024
Link: https://doi.org/10.1016/..
 
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2

Phenotypic heterogeneity associated with KIF21A: Two new ca..:

Bhola, Priya T. ; Mishra, Radha ; Posey, Jennifer E....
American Journal of Medical Genetics Part A.  194 (2023)  3 - p. , 2023
Link: https://doi.org/10.1002/..
 
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3

RNA sequencing to support intronic variant interpretation: ..:

Bhola, Priya T. ; Marshall, Aren E. ; Liang, Yijing...
American Journal of Medical Genetics Part A.  191 (2023)  6 - p. 1664-1668 , 2023
Link: https://doi.org/10.1002/..
 
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4

HomozygousWNT9Bvariants in two families with bilateral rena..:

Lemire, Gabrielle ; Zheng, Bixia ; Ediae, Grace U....
American Journal of Medical Genetics Part A.  185 (2021)  10 - p. 3005-3011 , 2021
Link: https://doi.org/10.1002/..
 
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5

A pilot eConsultation service in Eastern Ontario: bridging ..:

Bhola, Priya T. ; Liddy, Clare ; Afkham, Amir..
European Journal of Human Genetics.  27 (2019)  7 - p. 1026-1032 , 2019
Link: https://doi.org/10.1038/..
 
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6

A retrospective review of 48 individuals, including 12 fami..:

Bhola, Priya T. ; Gilpin, Cathy ; Smith, Amanda.
Familial Cancer.  17 (2018)  4 - p. 615-620 , 2018
Link: https://doi.org/10.1007/..
 
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7

Autosomal dominant cutis laxa with progeroid features due t..:

Bhola, Priya T ; Hartley, Taila ; Bareke, Eric...
Journal of Human Genetics.  62 (2017)  6 - p. 661-663 , 2017
Link: https://doi.org/10.1038/..
 
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8

Self‐Assembling Peptide as a Potential Carrier for Hydropho..:

Fung, Shan Yu ; Yang, Hong ; Bhola, Priya T....
Advanced Functional Materials.  19 (2008)  1 - p. 74-83 , 2008
Link: https://doi.org/10.1002/..
 
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9

Elucidating the clinical and molecular spectrum of SMARCC2-..:

Bosch, Elisabeth ; Popp, Bernt ; Güse, Esther...
https://research.vumc.nl/en/publications/47b00604-c0fa-431e-b4dc-67690fdf85b9.  , 2023
Link: https://research.vumc.nl..
 
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10

Elucidating the clinical and molecular spectrum of SMARCC2-..:

Bosch, Elisabeth ; Popp, Bernt ; Güse, Esther...
https://research.vumc.nl/en/publications/47b00604-c0fa-431e-b4dc-67690fdf85b9.  , 2023
Link: https://research.vumc.nl..
 
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11

Elucidating the clinical and molecular spectrum of SMARCC2-..:

Bosch, Elisabeth ; Popp, Bernt ; Güse, Esther...
https://research.rug.nl/en/publications/eab0ba2a-eda7-42fc-bc42-e9859dc89f35.  , 2023
Link: https://hdl.handle.net/1..
 
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12

P375: Case study: Germline chromoanagenesis associated with..:

Bhola, Priya ; Marshall, Aren ; Bergeron, Melanie Beaulieu..
Genetics in Medicine Open.  2 (2024)  - p. 101269 , 2024
Link: https://doi.org/10.1016/..
 
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13

Yunis-Varón syndrome caused by biallelic VAC14 mutations:

Care4Rare Consortium ; Lines, Matthew A ; Ito, Yoko...
European Journal of Human Genetics.  25 (2017)  9 - p. 1049-1054 , 2017
Link: https://doi.org/10.1038/..
 
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14

Preclinical in vivo evaluation of rapamycin in human malign..:

Bhola, Priya ; Banerjee, Sutapa ; Mukherjee, Joydeep...
International Journal of Cancer.  126 (2009)  2 - p. 563-571 , 2009
Link: https://doi.org/10.1002/..
 
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15

To Change or Not to Change? A Study regarding the Satisfact..:

Eenshuistra, Annika ; Bhola, Priscilla M. ; Hoek-Dekker, Ariënne J...
Child & Youth Services.  44 (2022)  3 - p. 300-327 , 2022
Link: https://doi.org/10.1080/..
 
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