Feng Y - Search Results

1

DNA Variant in the RPGRIP1L Gene Influences Alternative Splicing.

Reble E, Feng Y, Wigg KG, Barr CL. Reble E, et al. Among authors: feng y. Mol Neuropsychiatry. 2020 Apr;5(Suppl 1):97-106. doi: 10.1159/000502199. Epub 2019 Sep 25. Mol Neuropsychiatry. 2020. PMID: 32399473 Free PMC article.

2

Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder.

Barr CL, Feng Y, Wigg K, Bloom S, Roberts W, Malone M, Schachar R, Tannock R, Kennedy JL. Barr CL, et al. Among authors: feng y. Mol Psychiatry. 2000 Jul;5(4):405-9. doi: 10.1038/sj.mp.4000733. Mol Psychiatry. 2000. PMID: 10889551

3

Attention-deficit hyperactivity disorder and the gene for the dopamine D5 receptor.

Barr CL, Wigg KG, Feng Y, Zai G, Malone M, Roberts W, Schachar R, Tannock R, Kennedy JL. Barr CL, et al. Among authors: feng y. Mol Psychiatry. 2000 Sep;5(5):548-51. doi: 10.1038/sj.mp.4000777. Mol Psychiatry. 2000. PMID: 11032390

4

Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder.

Barr CL, Xu C, Kroft J, Feng Y, Wigg K, Zai G, Tannock R, Schachar R, Malone M, Roberts W, Nöthen MM, Grünhage F, Vandenbergh DJ, Uhl G, Sunohara G, King N, Kennedy JL. Barr CL, et al. Among authors: feng y. Biol Psychiatry. 2001 Feb 15;49(4):333-9. doi: 10.1016/s0006-3223(00)01053-2. Biol Psychiatry. 2001. PMID: 11239904

5

5'-untranslated region of the dopamine D4 receptor gene and attention-deficit hyperactivity disorder.

Barr CL, Feng Y, Wigg KG, Schachar R, Tannock R, Roberts W, Malone M, Kennedy JL. Barr CL, et al. Among authors: feng y. Am J Med Genet. 2001 Jan 8;105(1):84-90. Am J Med Genet. 2001. PMID: 11425008

6

The norepinephrine transporter gene and attention-deficit hyperactivity disorder.

Barr CL, Kroft J, Feng Y, Wigg K, Roberts W, Malone M, Ickowicz A, Schachar R, Tannock R, Kennedy JL. Barr CL, et al. Among authors: feng y. Am J Med Genet. 2002 Apr 8;114(3):255-9. doi: 10.1002/ajmg.10193. Am J Med Genet. 2002. PMID: 11920844

7

Support for EKN1 as the susceptibility locus for dyslexia on 15q21.

Wigg KG, Couto JM, Feng Y, Anderson B, Cate-Carter TD, Macciardi F, Tannock R, Lovett MW, Humphries TW, Barr CL. Wigg KG, et al. Among authors: feng y. Mol Psychiatry. 2004 Dec;9(12):1111-21. doi: 10.1038/sj.mp.4001543. Mol Psychiatry. 2004. PMID: 15249932 Clinical Trial.

8

Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.

Paschou P, Feng Y, Pakstis AJ, Speed WC, DeMille MM, Kidd JR, Jaghori B, Kurlan R, Pauls DL, Sandor P, Barr CL, Kidd KK. Paschou P, et al. Among authors: feng y. Am J Hum Genet. 2004 Oct;75(4):545-60. doi: 10.1086/424389. Epub 2004 Aug 9. Am J Hum Genet. 2004. PMID: 15303240 Free PMC article.

9

Sequence variation in the 3'-untranslated region of the dopamine transporter gene and attention-deficit hyperactivity disorder (ADHD).

Feng Y, Wigg KG, Makkar R, Ickowicz A, Pathare T, Tannock R, Roberts W, Malone M, Kennedy JL, Schachar R, Barr CL. Feng Y, et al. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):1-6. doi: 10.1002/ajmg.b.30190. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16082693

10

The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder.

Feng Y, Crosbie J, Wigg K, Pathare T, Ickowicz A, Schachar R, Tannock R, Roberts W, Malone M, Swanson J, Kennedy JL, Barr CL. Feng Y, et al. Mol Psychiatry. 2005 Nov;10(11):998-1005, 973. doi: 10.1038/sj.mp.4001722. Mol Psychiatry. 2005. PMID: 16088329

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