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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 1
2000 1
2001 2
2002 2
2003 2
2004 3
2005 4
2006 2
2007 1
2008 2
2009 3
2010 4
2011 10
2012 4
2013 4
2014 5
2015 3
2016 1
2017 5
2018 3
2019 1
2020 4
2023 1
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61 results
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Page 1
Family history: the three-generation pedigree.
Wattendorf DJ, Hadley DW. Wattendorf DJ, et al. Among authors: hadley dw. Am Fam Physician. 2005 Aug 1;72(3):441-8. Am Fam Physician. 2005. PMID: 16100858 Free article. Review.
Genetic testing in Parkinson's disease.
McInerney-Leo A, Hadley DW, Gwinn-Hardy K, Hardy J. McInerney-Leo A, et al. Among authors: hadley dw. Mov Disord. 2005 Jan;20(1):1-10. doi: 10.1002/mds.20316. Mov Disord. 2005. PMID: 15503301 Review.
The Human Genome Project: an update.
Peters KF, Menaker TJ, Wilson PL, Hadley DW. Peters KF, et al. Among authors: hadley dw. Cancer Nurs. 2001 Aug;24(4):287-92; quiz 292-3. doi: 10.1097/00002820-200108000-00007. Cancer Nurs. 2001. PMID: 11502037 Review.
An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) association.
Solomon BD, Baker LA, Bear KA, Cunningham BK, Giampietro PF, Hadigan C, Hadley DW, Harrison S, Levitt MA, Niforatos N, Paul SM, Raggio C, Reutter H, Warren-Mora N. Solomon BD, et al. Among authors: hadley dw. J Pediatr. 2014 Mar;164(3):451-7.e1. doi: 10.1016/j.jpeds.2013.10.086. Epub 2013 Dec 12. J Pediatr. 2014. PMID: 24332453 Free PMC article. Review. No abstract available.
SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly.
Stokes B, Berger SI, Hall BA, Weiss K, Martinez AF, Hadley DW, Murdock DR, Ramanathan S, Clark RD, Roessler E, Kruszka P, Muenke M. Stokes B, et al. Among authors: hadley dw. Congenit Anom (Kyoto). 2018 Jan;58(1):29-32. doi: 10.1111/cga.12234. Epub 2017 Aug 1. Congenit Anom (Kyoto). 2018. PMID: 28670735 Free PMC article.
Incidental medical information in whole-exome sequencing.
Solomon BD, Hadley DW, Pineda-Alvarez DE; NISC Comparative Sequencing Program; Kamat A, Teer JK, Cherukuri PF, Hansen NF, Cruz P, Young AC, Berkman BE, Chandrasekharappa SC, Mullikin JC. Solomon BD, et al. Among authors: hadley dw. Pediatrics. 2012 Jun;129(6):e1605-11. doi: 10.1542/peds.2011-0080. Epub 2012 May 14. Pediatrics. 2012. PMID: 22585771 Free PMC article.
Analysis of renal anomalies in VACTERL association.
Cunningham BK, Khromykh A, Martinez AF, Carney T, Hadley DW, Solomon BD. Cunningham BK, et al. Among authors: hadley dw. Birth Defects Res A Clin Mol Teratol. 2014 Oct;100(10):801-5. doi: 10.1002/bdra.23302. Epub 2014 Sep 5. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 25196458 Free PMC article.
61 results