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1

Development and assessment of educational materials for spi..:

Eichten, Carly ; Kuhl, Ashley ; Baker, Mei...
Journal of Genetic Counseling. , 2024

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

2

Leadership development in genetic counseling graduate progr..:

Polanski, Amanda ; Hall, April ; Reiser, Catherine..
Journal of Genetic Counseling. , 2024

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

3

No association between SCN9A and monogenic human epilepsy d..:

Fasham, James ; Leslie, Joseph S. ; Harrison, Jamie W....
PLOS Genetics. 16 (2020) 11 - p. e1009161 , 2020

Link: https://doi.org/10.1371/..

4

Familial segregation of a 5q15‐q21.2 deletion associated wi..:

Zepeda‐Mendoza, Cinthya ; Goodenberger, McKinsey L. ; Kuhl, Ashley..
Clinical Case Reports. 7 (2019) 6 - p. 1154-1160 , 2019

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

5

Newborn Screening for Inherited Metabolic Disorders: Early ..:

Held, Patrice K. ; Rice, Gregory M. ; Kuhl, Ashley...
Public Health Reports (1974-). 134 (2019) 2S - p. 58S-63S , 2019

Link: https://www.jstor.org/st..

6

Newborn Screening for Inherited Metabolic Disorders: Early ..:

Held, Patrice K. ; Rice, Gregory M. ; Kuhl, Ashley...
Public Health Reports. 134 (2019) 2_suppl - p. 58S-63S , 2019

Link: https://doi.org/10.1177/..

7

Pegylated asparaginase as cause of fatal hyperammonemia in ..:

Peters, Megan ; Zee‐Cheng, Janine ; Kuhl, Ashley...
Pediatric Blood & Cancer. 65 (2018) 9 - p. , 2018

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

8

Genotypes of patients with phenylalanine hydroxylase defici..:

Schwoerer, Jessica Scott ; Drilias, Nicoletta ; Kuhl, Ashley..
Molecular Genetics and Metabolism Reports. 15 (2018) - p. 75-77 , 2018

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

9

Development of carrier testing for common inborn errors of ..:

Kuhl, Ashley ; van Calcar, Sandra ; Baker, Mei...
Genetics in Medicine. 19 (2017) 3 - p. 352-356 , 2017

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

10

Genetic Counseling Graduate Student Debt: Impact on Program..:

Kuhl, Ashley ; Reiser, Catherine ; Eickhoff, Jens.
Journal of Genetic Counseling. 23 (2014) 5 - p. 824-837 , 2014

Link: https://doi.org/10.1007/..

11

No association between SCN9A and monogenic human epilepsy d..:

James Fasham ; Joseph S Leslie ; Jamie W Harrison...
https://doi.org/10.1371/journal.pgen.1009161. , 2020

Link: https://doi.org/10.1371/..

12

Familial segregation of a 5q15‐q21.2 deletion associated wi..:

Cinthya Zepeda‐Mendoza ; McKinsey L. Goodenberger ; Ashley Kuhl..
https://doi.org/10.1002/ccr3.2186. , 2019

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

13

Genotypes of patients with phenylalanine hydroxylase defici..:

Jessica Scott Schwoerer ; Nicoletta Drilias ; Ashley Kuhl..
http://www.sciencedirect.com/science/article/pii/S2214426917301337. , 2018

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

14

Contributors:

, In: The Handbook of Personality Dynamics and Processes,

Adler, Jonathan M. ; Alaybek, Balca ; Allen, Jayne L.... - p. xv-xviii , 2021

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

15

Classifying Drugs by their Arrhythmogenic Risk Using Machin..:

Sahli-Costabal, Francisco ; Seo, Kinya ; Ashley, Euan.
Biophysical Journal. 118 (2020) 5 - p. 1165-1176 , 2020

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

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