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Merrill, Shana L.
27
results:
Search for persons
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Online (27)
Mediatypes
Articles (Online) (14)
OpenAccess-fulltext (13)
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1
Embodied risk for families with Li-Fraumeni syndrome: Like ..:
Werner-Lin, Allison
;
Forbes Shepherd, Rowan
;
Young, Jennifer L.
...
Social Science & Medicine. 301 (2022) - p. 114905 , 2022
Link:
https://doi.org/10.1016/..
?
2
Fanconi anemia caused by biallelic inactivation of BRCA2 ca..:
Maxwell, Kara N.
;
Patel, Vishal
;
Nead, Kevin T.
...
Clinical Genetics. 103 (2022) 1 - p. 119-124 , 2022
Link:
https://doi.org/10.1111/..
?
3
Family Identity and Roles in the Context of Li-Fraumeni Syn..:
Wilsnack, Catherine
;
Young, Jennifer L.
;
Merrill, Shana L.
...
Health & Social Work. 46 (2021) 4 - p. 299-307 , 2021
Link:
https://doi.org/10.1093/..
?
4
Waiting and "weighted down": the challenge of anticipatory ..:
Werner-Lin, Allison
;
Young, Jennifer L.
;
Wilsnack, Catherine
...
Familial Cancer. 19 (2020) 3 - p. 259-268 , 2020
Link:
https://doi.org/10.1007/..
?
5
Correction to: Talking with Children about Adult‐Onset Here..:
Werner‐Lin, Allison
;
Merrill, Shana L.
;
Brandt, Amanda C.
..
Journal of Genetic Counseling. 27 (2018) 6 - p. 1523-1523 , 2018
Link:
https://doi.org/10.1007/..
?
6
Talking with Children About Adult‐Onset Hereditary Cancer R..:
Werner‐Lin, Allison
;
Merrill, Shana L.
;
Brandt, Amanda C.
Journal of Genetic Counseling. 27 (2018) 3 - p. 533-548 , 2018
Link:
https://doi.org/10.1007/..
?
7
Gain of Function for the SCN1A/hNav1.1-L1670W Mutation Resp..:
Dhifallah, Sandra
;
Lancaster, Eric
;
Merrill, Shana
...
Frontiers in Molecular Neuroscience. 11 (2018) - p. , 2018
Link:
https://doi.org/10.3389/..
?
8
Aggregates of Mutant DNMT1 Are Linked to a Spectrum of Neur..:
Baets, Jonathan
;
Duan, Xiaohui
;
Wu, Yanhong
...
Neurology. 84 (2015) 14_supplement - p. , 2015
Link:
https://doi.org/10.1212/..
?
9
Is it Time for Genomic Counseling? Retrofitting Genetic Cou..:
Merrill, Shana L.
;
Guthrie, Kimberly J.
Current Genetic Medicine Reports. 3 (2015) 2 - p. 57-64 , 2015
Link:
https://doi.org/10.1007/..
?
10
Development of a tiered and binned genetic counseling model..:
Bradbury, Angela R.
;
Patrick-Miller, Linda
;
Long, Jessica
...
Genetics in Medicine. 17 (2015) 6 - p. 485-492 , 2015
Link:
https://doi.org/10.1038/..
?
11
Defects of mutant DNMT1 are linked to a spectrum of neurolo..:
Baets, Jonathan
;
Duan, Xiaohui
;
Wu, Yanhong
...
Brain. 138 (2015) 4 - p. 845-861 , 2015
Link:
https://doi.org/10.1093/..
?
12
Ethical Challenges of the Use of Whole Exome Sequencing in ..:
Merrill, Shana L.
;
Vaidya, Anjali
;
Pyeritz, Reed E.
World Journal for Pediatric and Congenital Heart Surgery. 4 (2013) 1 - p. 58-61 , 2013
Link:
https://doi.org/10.1177/..
?
13
Inherited Mutations in Pheochromocytoma and Paraganglioma: ..:
Fishbein, Lauren
;
Merrill, Shana
;
Fraker, Douglas L.
..
Annals of Surgical Oncology. 20 (2013) 5 - p. 1444-1450 , 2013
Link:
https://doi.org/10.1245/..
?
14
Fanconi Anemia caused by biallelic inactivation of BRCA2 ca..:
Maxwell, Kara N
;
Patel, Vishal
;
Nead, Kevin T
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742260/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
15
Embodied risk for families with Li-Fraumeni syndrome: Like ..:
Werner-Lin, Allison
;
Shepherd, Rowan Forbes
;
Young, Jennifer L
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9237847/. , 2022
Link:
http://www.ncbi.nlm.nih...
1-15