Wildin R - Search Results

Year	Number of Results
1964	1
1965	1
1981	1
1982	1
1984	1
1986	1
1991	1
1994	1
1995	1
1998	2
1999	2
2001	2
2002	1
2003	1
2004	1
2005	2
2010	1
2011	1
2012	2
2014	1
2016	2
2017	1
2018	1
2020	2
2021	2
2022	2
2023	1
2024	2

1

Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and Projects.

Volpi S, Bult CJ, Chisholm RL, Deverka PA, Ginsburg GS, Jacob HJ, Kasapi M, McLeod HL, Roden DM, Williams MS, Green ED, Rodriguez LL, Aronson S, Cavallari LH, Denny JC, Dressler LG, Johnson JA, Klein TE, Leeder JS, Piquette-Miller M, Perera M, Rasmussen-Torvik LJ, Rehm HL, Ritchie MD, Skaar TC, Wagle N, Weinshilboum R, Weitzel KW, Wildin R, Wilson J, Manolio TA, Relling MV. Volpi S, et al. Among authors: wildin r. Clin Pharmacol Ther. 2018 May;103(5):778-786. doi: 10.1002/cpt.1048. Epub 2018 Mar 30. Clin Pharmacol Ther. 2018. PMID: 29460415 Free PMC article. Review.

2

IPEX and FOXP3: clinical and research perspectives.

Wildin RS, Freitas A. Wildin RS, et al. J Autoimmun. 2005;25 Suppl:56-62. doi: 10.1016/j.jaut.2005.04.008. Epub 2005 Oct 21. J Autoimmun. 2005. PMID: 16243487 Review.

3

Cost Effectiveness of Genomic Population Health Screening in Adults: A Review of Modeling Studies and Future Directions.

Wildin RS. Wildin RS. J Appl Lab Med. 2024 Jan 3;9(1):92-103. doi: 10.1093/jalm/jfad093. J Appl Lab Med. 2024. PMID: 38167759 Review.

4

Modernizing family health history: achievable strategies to reduce implementation gaps.

Wildin RS, Messersmith DJ, Houwink EJF. Wildin RS, et al. J Community Genet. 2021 Jul;12(3):493-496. doi: 10.1007/s12687-021-00531-6. Epub 2021 May 24. J Community Genet. 2021. PMID: 34028705 Free PMC article.

5

Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome.

Wildin RS, Smyk-Pearson S, Filipovich AH. Wildin RS, et al. J Med Genet. 2002 Aug;39(8):537-45. doi: 10.1136/jmg.39.8.537. J Med Genet. 2002. PMID: 12161590 Free PMC article. Review.

6

Primary Care Implementation of Genomic Population Health Screening Using a Large Gene Sequencing Panel.

Wildin RS, Giummo CA, Reiter AW, Peterson TC, Leonard DGB. Wildin RS, et al. Front Genet. 2022 Apr 25;13:867334. doi: 10.3389/fgene.2022.867334. eCollection 2022. Front Genet. 2022. PMID: 35547253 Free PMC article.

7

Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genes.

Qiao Y, Mondal K, Trapani V, Wen J, Carpenter G, Wildin R, Price EM, Gibbons RJ, Eichmeyer J, Jiang R, DuPont B, Martell S, Lewis SM, Robinson WP, O'Driscoll M, Wolf FI, Zwick ME, Rajcan-Separovic E. Qiao Y, et al. Among authors: wildin r. Hum Mutat. 2014 Jan;35(1):58-62. doi: 10.1002/humu.22465. Hum Mutat. 2014. PMID: 24130152

8

Real-World Results from Combined Screening for Monogenic Genomic Health Risks and Reproductive Risks in 300 Adults.

Wildin RS, Gerrard DL, Leonard DGB. Wildin RS, et al. J Pers Med. 2022 Nov 28;12(12):1962. doi: 10.3390/jpm12121962. J Pers Med. 2022. PMID: 36556183 Free PMC article.

9

Case 1: A 31-week Fetus with Intestinal Atresia and Sudden Fetal Hemorrhage.

Pahl A, Wildin R, Wills M, Barkhuff W. Pahl A, et al. Among authors: wildin r. Neoreviews. 2020 Nov;21(11):e761-e764. doi: 10.1542/neo.21-11-e761. Neoreviews. 2020. PMID: 33139513 No abstract available.

10

Novel neonatal presentation of megalencephaly-polymicrogyria-pigmentary mosaicism syndrome (MPPM) related to MTOR mutation: Report of a case.

Taylor DL, Wildin RS, Morley KW. Taylor DL, et al. Among authors: wildin rs. Pediatr Dermatol. 2021 Mar;38(2):536-537. doi: 10.1111/pde.14480. Epub 2020 Dec 16. Pediatr Dermatol. 2021. PMID: 33325571

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