Suchergebnisse - "Carroll, June C"

PubPharm (181)

1

Genetics providers' perspectives on the use of digital tools in clinical practice

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2024

von Lee, W. | Hirjikaka, D. | Grewal, S. | +40

2

"I don't need any more unknowns hanging over my head" : Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2023

von Shickh, S. | Mighton, C. | Clausen, M. | +46

3

A model for the return and referral of all clinically significant secondary findings of genomic sequencing

enthalten in: Journal of medical genetics | 2023

von Kodida, R. | Reble, E. | Clausen, M. | +59

4

Great expectations : patients' preferences for clinically significant results from genomic sequencing

enthalten in: Human genetics | 2023

von Shickh, S. | Sebastian, A. | Clausen, M. | +50

5

Finding the sweet spot : a qualitative study exploring patients' acceptability of chatbots in genetic service delivery

enthalten in: Human genetics | 2023

von Luca, S. | Clausen, M. | Shaw, A. | +36

6

Great expectations: patients’ preferences for clinically significant results from genomic sequencing

enthalten in: Human genetics | 2023

von Shickh, S. | Sebastian, A. | Clausen, M. | +13

7

A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings

enthalten in: Human genetics | 2022

von Sam, J. | Reble, E. | Kodida, R. | +21

8

Use of eConsult to enhance genetics service delivery in primary care : A multimethod study

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2022

von Carroll, J. | Liddy, C. | Afkham, A. | +11

9

A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings

enthalten in: Human genetics | 2022

von Sam, J. | Reble, E. | Kodida, R. | +20

10

A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings

enthalten in: Human genetics | 2022

von Sam, J. | Reble, E. | Kodida, R. | +20

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