E-LIB Suche - Ergebnisse für: Ghazani, Arezou A.

1

Diagnosis of Two Unrelated Syndromes of Prader-Willi and Ca..:

Cuk, Mario ; Unal, Busra ; Bevanda, Andjela...
Genes. 15 (2024) 7 - p. 946 , 2024

Link: https://doi.org/10.3390/..

2

Genomic disparity impacts variant classification of cancer ..:

Agaoglu, Nihat B. ; Unal, Busra ; Hayes, Connor P....
Cancer Medicine. 13 (2024) 3 - p. , 2024

Link: https://doi.org/10.1002/..

3

Development and evaluation of INT2GRATE: a platform for com..:

Isidro, Raymond A. ; Chittenden, Anu ; Walker, McKenzie...
Frontiers in Oncology. 13 (2024) - p. , 2024

Link: https://doi.org/10.3389/..

4

Advancing Precision Oncology in Hereditary Paraganglioma-Ph..:

Rana, Huma Q. ; Koeller, Diane R. ; Walker, McKenzie...
Cancers. 16 (2024) 5 - p. 947 , 2024

Link: https://doi.org/10.3390/..

5

An optimized protocol for evaluating pathogenicity of VHL g..:

Koeller, Diane R. ; Manning, Danielle K. ; Schwartz, Alison...
MethodsX. 9 (2022) - p. 101761 , 2022

Link: https://doi.org/10.1016/..

6

Vulvar Melanoma in association with germline MITF p.E318K v..:

Koeller, Diane R. ; Schwartz, Alison ; DeSimone, Mia S....
Cancer Genetics. 262-263 (2022) - p. 102-106 , 2022

Link: https://doi.org/10.1016/..

7

Concurrent Pathogenic Variants of BRCA1, MUTYH and CHEK2 in..:

Agaoglu, Nihat Bugra ; Ng, Ozden Hatirnaz ; Unal, Busra...
Cancer Genetics. 268-269 (2022) - p. 128-136 , 2022

Link: https://doi.org/10.1016/..

8

An integrated somatic and germline approach to aid interpre..:

Schwartz, Alison ; Manning, Danielle K. ; Koeller, Diane R....
Frontiers in Oncology. 12 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

9

Pathogenicity of VHL variants in families with non-syndromi..:

Rana, Huma Q. ; Koeller, Diane R. ; Schwartz, Alison...
European Journal of Medical Genetics. 64 (2021) 12 - p. 104359 , 2021

Link: https://doi.org/10.1016/..

10

Assessment of genomic alterations in non-syndromic von Hipp..:

Manning, Danielle K. ; Shivdasani, Priyanka ; Koeller, Diane R....
Data in Brief. 39 (2021) - p. 107653 , 2021

Link: https://doi.org/10.1016/..

11

Correction: Secondary findings from clinical genomic sequen..:

Hart, M. Ragan ; Biesecker, Barbara B. ; Blout, Carrie L....
Genetics in Medicine. 21 (2019) 5 - p. 1261-1262 , 2019

Link: https://doi.org/10.1038/..

12

Secondary findings from clinical genomic sequencing: preval..:

Hart, M. Ragan ; Biesecker, Barbara B. ; Blout, Carrie L....
Genetics in Medicine. 21 (2019) 5 - p. 1100-1110 , 2019

Link: https://doi.org/10.1038/..

13

Approaches to carrier testing and results disclosure in tra..:

Porter, Kathryn M. ; Kauffman, Tia L. ; Koenig, Barbara A....
Molecular Genetics & Genomic Medicine. 6 (2018) 6 - p. 898-909 , 2018

Link: https://doi.org/10.1002/..

14

A survey of current practices for genomic sequencing test i..:

O'Daniel, Julianne M. ; McLaughlin, Heather M. ; Amendola, Laura M....
Genetics in Medicine. 19 (2017) 5 - p. 575-582 , 2017

Link: https://doi.org/10.1038/..

15

Point of care assessment of melanoma tumor signaling and me..:

Gee, Michael S. ; Ghazani, Arezou A. ; Haq, Rizwan...
Nanomedicine: Nanotechnology, Biology and Medicine. 13 (2017) 3 - p. 821-828 , 2017

Link: https://doi.org/10.1016/..