Valdez R - Search Results

1

PhenX measures for phenotyping rare genetic conditions.

Phillips M, Grant T, Giampietro P, Bodurtha J, Valdez R, Maiese DR, Hendershot T, Terry SF, Hamilton CM. Phillips M, et al. Among authors: valdez r. Genet Med. 2017 Jul;19(7):834-837. doi: 10.1038/gim.2016.199. Epub 2017 Jan 12. Genet Med. 2017. PMID: 28079902 Free PMC article.

2

The need for a next-generation public health response to rare diseases.

Valdez R, Grosse SD, Khoury MJ. Valdez R, et al. Genet Med. 2016 Oct 27;19(5):489-490. doi: 10.1038/gim.2016.166. Epub 2016 Oct 27. Genet Med. 2016. PMID: 27787501 Free PMC article. No abstract available.

3

Evaluation of family history as a risk factor and screening tool for detecting undiagnosed diabetes in a nationally representative survey population.

Hariri S, Yoon PW, Moonesinghe R, Valdez R, Khoury MJ. Hariri S, et al. Among authors: valdez r. Genet Med. 2006 Dec;8(12):752-9. doi: 10.1097/01.gim.0000250205.73963.f3. Genet Med. 2006. PMID: 17172938 Free article.

4

The association between family history of asthma and the prevalence of asthma among US adults: National Health and Nutrition Examination Survey, 1999-2004.

Liu T, Valdez R, Yoon PW, Crocker D, Moonesinghe R, Khoury MJ. Liu T, et al. Among authors: valdez r. Genet Med. 2009 May;11(5):323-8. doi: 10.1097/GIM.0b013e31819d3015. Genet Med. 2009. PMID: 19452621 Free article.

5

Family history of type 2 diabetes: a population-based screening tool for prevention?

Hariri S, Yoon PW, Qureshi N, Valdez R, Scheuner MT, Khoury MJ. Hariri S, et al. Among authors: valdez r. Genet Med. 2006 Feb;8(2):102-8. doi: 10.1097/01.gim.0000200949.52795.df. Genet Med. 2006. PMID: 16481893 Free article.

6

Clinical utility of family history for cancer screening and referral in primary care: a report from the Family Healthware Impact Trial.

Rubinstein WS, Acheson LS, O'Neill SM, Ruffin MT 4th, Wang C, Beaumont JL, Rothrock N; Family Healthware Impact Trial (FHITr) Group. Rubinstein WS, et al. Genet Med. 2011 Nov;13(11):956-65. doi: 10.1097/GIM.0b013e3182241d88. Genet Med. 2011. PMID: 22075527 Free PMC article. Clinical Trial.

7

Public Health and Rare Diseases: Oxymoron No More.

Valdez R, Ouyang L, Bolen J. Valdez R, et al. Prev Chronic Dis. 2016 Jan 14;13:E05. doi: 10.5888/pcd13.150491. Prev Chronic Dis. 2016. PMID: 26766846 Free PMC article. No abstract available.

8

The effect of steroid treatment on weight in nonambulatory males with Duchenne muscular dystrophy.

Lamb MM, Cai B, Royer J, Pandya S, Soim A, Valdez R, DiGuiseppi C, James K, Whitehead N, Peay H, Venkatesh SY, Matthews D; Muscular Dystrophy Surveillance, Research, and Tracking Network (MD STARnet). Lamb MM, et al. Among authors: valdez r. Am J Med Genet A. 2018 Nov;176(11):2350-2358. doi: 10.1002/ajmg.a.40517. Epub 2018 Sep 26. Am J Med Genet A. 2018. PMID: 30256515 Free PMC article.

9

Family history and perceptions about risk and prevention for chronic diseases in primary care: a report from the family healthware impact trial.

Acheson LS, Wang C, Zyzanski SJ, Lynn A, Ruffin MT 4th, Gramling R, Rubinstein WS, O'Neill SM, Nease DE Jr; Family Healthware Impact Trial (FHITr) Group. Acheson LS, et al. Genet Med. 2010 Apr;12(4):212-8. doi: 10.1097/GIM.0b013e3181d56ae6. Genet Med. 2010. PMID: 20216073 Free PMC article. Clinical Trial.

10

A Review of MD STAR net's Research Contributions to Pediatric-Onset Dystrophinopathy in the United States; 2002-2017.

Sahay KM, Smith T, Conway KM, Romitti PA, Lamb MM, Andrews J, Pandya S, Oleszek J, Cunniff C, Valdez R. Sahay KM, et al. Among authors: valdez r. J Child Neurol. 2019 Jan;34(1):44-53. doi: 10.1177/0883073818801704. Epub 2018 Oct 22. J Child Neurol. 2019. PMID: 30345857 Free PMC article. Review.

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