E-LIB Suche - Ergebnisse für: Dorschner, Michael O

1

Feasibility of an electronic patient-facing cancer family h..:

Feigelson, Heather Spencer ; Mittendorf, Kathleen F. ; Okuyama, Sonia...
Genetics in Medicine Open. , 2024

2

NOTCH3 C201R variant causes cerebral autosomal dominant art..:

Korvatska, Olena ; Bucks, Stephanie A. ; Yoda, Rebecca A....
Journal of the Neurological Sciences. 452 (2023) - p. 120763 , 2023

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

3

Most people share genetic test results with relatives even ..:

Hunter, Jessica Ezzell ; Riddle, Leslie ; Joseph, Galen...
Genetics in Medicine. 25 (2023) 11 - p. 100923 , 2023

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

4

ORCA, a values-based decision aid for selecting additional ..:

Liles, Elizabeth G. ; Leo, Michael C. ; Freed, Amanda S....
Genetics in Medicine. 24 (2022) 8 - p. 1664-1674 , 2022

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

5

Homozygous CADPS2 Mutations Cause Neurodegenerative Disease..:

Lorenzo‐Betancor, Oswaldo ; Galosi, Livio ; Bonfili, Laura...
Movement Disorders. 37 (2022) 12 - p. 2345-2354 , 2022

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

6

An accessible, relational, inclusive, and actionable (ARIA)..:

Joseph, Galen ; Leo, Michael C. ; Riddle, Leslie...
Genetics in Medicine. 24 (2022) 11 - p. 2228-2239 , 2022

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

7

Corrigendum to "Cancer Health Assessments Reaching Many (CH..:

Mittendorf, Kathleen F. ; Kauffman, Tia L. ; Amendola, Laura M....
Contemporary Clinical Trials. 114 (2022) - p. 106682 , 2022

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

8

Somatic Mosaicism of a PDGFRB Activating Variant in Aneurys..:

Parada, Carolina A. ; El‐Ghazali, Fatima M. ; Toglia, Daphne...
Journal of the American Heart Association. 11 (2022) 4 - p. , 2022

Link: https://doi.org/10.1161/..

9

Homozygous CADPS2 mutations cause neurodegenerative disease..:

Lorenzo-Betancor, Oswaldo ; Galosi, Livio ; Bonfili, Laura...
Neurology. 98 (2022) 18_supplement - p. , 2022

Link: https://doi.org/10.1212/..

10

Laboratory-related outcomes from integrating an accessible ..:

Amendola, Laura M. ; Shuster, Elizabeth ; Leo, Michael C....
Genetics in Medicine. 24 (2022) 6 - p. 1196-1205 , 2022

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

11

Cancer Health Assessments Reaching Many (CHARM): A clinical..:

Mittendorf, Kathleen F. ; Kauffman, Tia L. ; Amendola, Laura M....
Contemporary Clinical Trials. 106 (2021) - p. 106432 , 2021

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

12

Genetic counseling for early onset and familial dementia: P..:

Rolf, Bradley ; Blue, Elizabeth E. ; Bucks, Stephanie..
Journal of Genetic Counseling. 30 (2021) 3 - p. 793-802 , 2021

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

13

Triggering Receptor Expressed on Myeloid Cell 2 R47H Exacer..:

Korvatska, Olena ; Kiianitsa, Kostantin ; Ratushny, Alexander...
Frontiers in Immunology. 11 (2020) - p. , 2020

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

14

Alternative splicing in a presenilin 2 variant associated w..:

Braggin, Jacquelyn E. ; Bucks, Stephanie A. ; Course, Meredith M....
Annals of Clinical and Translational Neurology. 6 (2019) 4 - p. 762-777 , 2019

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

15

Clinical exome sequencing vs. usual care for hereditary col..:

Niu, Xin ; Amendola, Laura M. ; Hart, Ragan...
Contemporary Clinical Trials. 84 (2019) - p. 105820 , 2019

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