Ali N - Search Results

1

Women's healthcare providers' knowledge and practices surrounding fragile-X associated primary ovarian insufficiency (FXPOI).

Singleton AL, Hipp HS, Ali N, Poteet B, Allen EG. Singleton AL, et al. Among authors: ali n. J Assist Reprod Genet. 2024 Dec 6. doi: 10.1007/s10815-024-03337-w. Online ahead of print. J Assist Reprod Genet. 2024. PMID: 39641836

2

The diagnostic experience of women with fragile X-associated primary ovarian insufficiency (FXPOI).

Poteet B, Ali N, Bellcross C, Sherman SL, Espinel W, Hipp H, Allen EG. Poteet B, et al. Among authors: ali n. J Assist Reprod Genet. 2023 Jan;40(1):179-190. doi: 10.1007/s10815-022-02671-1. Epub 2022 Nov 30. J Assist Reprod Genet. 2023. PMID: 36447079 Free PMC article.

3

Healthcare Experiences of African American Women with the Fragile X Premutation.

King AP, Ali N, Bellcross C, Ehivet F, Hipp HS, Vaughn J, Allen EG. King AP, et al. Among authors: ali n. J Racial Ethn Health Disparities. 2024 Dec;11(6):3390-3400. doi: 10.1007/s40615-023-01792-2. Epub 2023 Sep 15. J Racial Ethn Health Disparities. 2024. PMID: 37713166 Free PMC article.

4

Primary Care Providers' Use of Genetic Services in the Southeast United States: Barriers, Facilitators, and Strategies.

Seibel E, Gunn G, Ali N, Jordan E, Kenneson A. Seibel E, et al. Among authors: ali n. J Prim Care Community Health. 2022 Jan-Dec;13:21501319221134752. doi: 10.1177/21501319221134752. J Prim Care Community Health. 2022. PMID: 36345220 Free PMC article.

5

Men with an FMR1 premutation and their health education needs.

Walsh MB, Charen K, Shubeck L, McConkie-Rosell A, Ali N, Bellcross C, Sherman SL. Walsh MB, et al. Among authors: ali n. J Genet Couns. 2021 Aug;30(4):1156-1167. doi: 10.1002/jgc4.1399. Epub 2021 Mar 31. J Genet Couns. 2021. PMID: 33788978 Free PMC article.

6

Poor recall of genetics curriculum by medical students highlights barriers to use in clinical practice.

Kapur S, Lichten L, Ali N, Garber KB. Kapur S, et al. Among authors: ali n. J Genet Couns. 2024 Feb;33(1):179-188. doi: 10.1002/jgc4.1795. Epub 2023 Sep 21. J Genet Couns. 2024. PMID: 37735936

7

Patients' perspectives on newborn screening for later-onset lysosomal storage diseases.

Lisi EC, Gillespie S, Laney D, Ali N. Lisi EC, et al. Among authors: ali n. Mol Genet Metab. 2016 Sep;119(1-2):109-14. doi: 10.1016/j.ymgme.2016.07.009. Epub 2016 Jul 21. Mol Genet Metab. 2016. PMID: 27591925

8

Impact of Implementing B-RST^TM to Screen for Hereditary Breast and Ovarian Cancer on Risk Perception and Genetic Counseling Uptake Among Women in an Academic Safety Net Hospital.

Wernke K, Bellcross C, Gabram S, Ali N, Stanislaw C. Wernke K, et al. Among authors: ali n. Clin Breast Cancer. 2019 Aug;19(4):e547-e555. doi: 10.1016/j.clbc.2019.02.014. Epub 2019 Mar 11. Clin Breast Cancer. 2019. PMID: 31005475

9

Assessment of a novel genetic counselling intervention to inform assisted reproductive technology treatments and other family-building options in adults with cystic fibrosis.

Kushary S, Ali N, Spencer JB, Dokson J, Hunt WR. Kushary S, et al. Among authors: ali n. Reprod Biomed Soc Online. 2021 Jun 4;13:37-45. doi: 10.1016/j.rbms.2021.05.001. eCollection 2021 Aug. Reprod Biomed Soc Online. 2021. PMID: 34195396 Free PMC article.

10

Health care practitioners' experience-based opinions on providing care after a positive newborn screen for Pompe disease.

Davids L, Sun Y, Moore RH, Lisi E, Wittenauer A, Wilcox WR, Ali N. Davids L, et al. Among authors: ali n. Mol Genet Metab. 2021 Sep-Oct;134(1-2):20-28. doi: 10.1016/j.ymgme.2021.09.001. Epub 2021 Sep 15. Mol Genet Metab. 2021. PMID: 34602357

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