Woodroffe A - Search Results

1

Molecular genetic delineation of a deletion of chromosome 13q12-->q13 in a patient with autism and auditory processing deficits.

Smith M, Woodroffe A, Smith R, Holguin S, Martinez J, Filipek PA, Modahl C, Moore B, Bocian ME, Mays L, Laulhere T, Flodman P, Spence MA. Smith M, et al. Among authors: woodroffe a. Cytogenet Genome Res. 2002;98(4):233-9. doi: 10.1159/000071040. Cytogenet Genome Res. 2002. PMID: 12826745

2

A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R.

Ramanathan S, Woodroffe A, Flodman PL, Mays LZ, Hanouni M, Modahl CB, Steinberg-Epstein R, Bocian ME, Spence MA, Smith M. Ramanathan S, et al. Among authors: woodroffe a. BMC Med Genet. 2004 Apr 16;5:10. doi: 10.1186/1471-2350-5-10. BMC Med Genet. 2004. PMID: 15090072 Free PMC article.

3

Candidate gene region for polycystic ovary syndrome on chromosome 19p13.2.

Urbanek M, Woodroffe A, Ewens KG, Diamanti-Kandarakis E, Legro RS, Strauss JF 3rd, Dunaif A, Spielman RS. Urbanek M, et al. Among authors: woodroffe a. J Clin Endocrinol Metab. 2005 Dec;90(12):6623-9. doi: 10.1210/jc.2005-0622. Epub 2005 Aug 9. J Clin Endocrinol Metab. 2005. PMID: 16091490

4

Ordered subset analysis supports a glaucoma locus at GLC1I on chromosome 15 in families with earlier adult age at diagnosis.

Woodroffe A, Krafchak CM, Fuse N, Lichter PR, Moroi SE, Schertzer R, Downs CA, Duren WL, Boehnke M, Richards JE. Woodroffe A, et al. Exp Eye Res. 2006 Jun;82(6):1068-74. doi: 10.1016/j.exer.2005.10.008. Epub 2005 Nov 18. Exp Eye Res. 2006. PMID: 16298363

5

Simple tests to detect errors in high-throughput genotype data in the molecular laboratory.

Vandenbergh DJ, Heron K, Peterson R, Shpargel KB, Woodroffe A, Blizard DA, McClearn GE, Vogler GP. Vandenbergh DJ, et al. Among authors: woodroffe a. J Biomol Tech. 2003 Mar;14(1):9-16. J Biomol Tech. 2003. PMID: 12901607 Free PMC article.

6

The Quality of Medication Treatment for Mental Disorders in the Department of Veterans Affairs and in Private-Sector Plans.

Watkins KE, Smith B, Akincigil A, Sorbero ME, Paddock S, Woodroffe A, Huang C, Crystal S, Pincus HA. Watkins KE, et al. Among authors: woodroffe a. Psychiatr Serv. 2016 Apr 1;67(4):391-6. doi: 10.1176/appi.ps.201400537. Epub 2015 Nov 16. Psychiatr Serv. 2016. PMID: 26567931

7

The quality of mental health care for veterans of Operation Enduring Freedom/Operation Iraqi Freedom.

Paddock SM, Woodroffe A, Watkins KE, Sorbero ME, Smith B, Mannle TE Jr, Solomon J, Pincus HA. Paddock SM, et al. Among authors: woodroffe a. Med Care. 2013 Jan;51(1):84-9. doi: 10.1097/MLR.0b013e318270bb6c. Med Care. 2013. PMID: 23032356

8

Care for veterans with mental and substance use disorders: good performance, but room to improve on many measures.

Watkins KE, Pincus HA, Paddock S, Smith B, Woodroffe A, Farmer C, Sorbero ME, Horvitz-Lennon M, Mannle T Jr, Hepner KA, Solomon J, Call C. Watkins KE, et al. Among authors: woodroffe a. Health Aff (Millwood). 2011 Nov;30(11):2194-203. doi: 10.1377/hlthaff.2011.0509. Epub 2011 Oct 19. Health Aff (Millwood). 2011. PMID: 22012967

9

Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans.

Xu B, Woodroffe A, Rodriguez-Murillo L, Roos JL, van Rensburg EJ, Abecasis GR, Gogos JA, Karayiorgou M. Xu B, et al. Among authors: woodroffe a. Proc Natl Acad Sci U S A. 2009 Sep 29;106(39):16746-51. doi: 10.1073/pnas.0908584106. Epub 2009 Sep 11. Proc Natl Acad Sci U S A. 2009. PMID: 19805367 Free PMC article.

10

Nogo Receptor 1 (RTN4R) as a candidate gene for schizophrenia: analysis using human and mouse genetic approaches.

Hsu R, Woodroffe A, Lai WS, Cook MN, Mukai J, Dunning JP, Swanson DJ, Roos JL, Abecasis GR, Karayiorgou M, Gogos JA. Hsu R, et al. Among authors: woodroffe a. PLoS One. 2007 Nov 28;2(11):e1234. doi: 10.1371/journal.pone.0001234. PLoS One. 2007. PMID: 18043741 Free PMC article.

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