Feng J - Search Results

1

Analysis of the neuroligin 4Y gene in patients with autism.

Yan J, Feng J, Schroer R, Li W, Skinner C, Schwartz CE, Cook EH Jr, Sommer SS. Yan J, et al. Among authors: feng j. Psychiatr Genet. 2008 Aug;18(4):204-7. doi: 10.1097/YPG.0b013e3282fb7fe6. Psychiatr Genet. 2008. PMID: 18628683

2

Mutation scanning of the androgen receptor gene in patients with psychiatric disorders reveals highly conserved variants in alcoholic and phobia patients.

Yan J, Feng J, Goldman D, Cook EH Jr, Craddock N, Jones IR, Heston LL, Sommer SS. Yan J, et al. Among authors: feng j. Psychiatr Genet. 2004 Mar;14(1):57-60. doi: 10.1097/00041444-200403000-00010. Psychiatr Genet. 2004. PMID: 15091318

3

MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism.

Shibayama A, Cook EH Jr, Feng J, Glanzmann C, Yan J, Craddock N, Jones IR, Goldman D, Heston LL, Sommer SS. Shibayama A, et al. Among authors: feng j. Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):50-3. doi: 10.1002/ajmg.b.30016. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15211631

4

Structural variants in the retinoid receptor genes in patients with schizophrenia and other psychiatric diseases.

Feng J, Chen J, Yan J, Jones IR, Craddock N, Cook EH Jr, Goldman D, Heston LL, Sommer SS. Feng J, et al. Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):50-3. doi: 10.1002/ajmg.b.30113. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15635645

5

High frequency of neurexin 1beta signal peptide structural variants in patients with autism.

Feng J, Schroer R, Yan J, Song W, Yang C, Bockholt A, Cook EH Jr, Skinner C, Schwartz CE, Sommer SS. Feng J, et al. Neurosci Lett. 2006 Nov 27;409(1):10-3. doi: 10.1016/j.neulet.2006.08.017. Epub 2006 Oct 10. Neurosci Lett. 2006. PMID: 17034946

6

Neurexin 1alpha structural variants associated with autism.

Yan J, Noltner K, Feng J, Li W, Schroer R, Skinner C, Zeng W, Schwartz CE, Sommer SS. Yan J, et al. Among authors: feng j. Neurosci Lett. 2008 Jun 27;438(3):368-70. doi: 10.1016/j.neulet.2008.04.074. Epub 2008 Apr 25. Neurosci Lett. 2008. PMID: 18490107

7

Systematic screening for mutations in the glycine receptor alpha2 subunit gene (GLRA2) in patients with schizophrenia and other psychiatric diseases.

Feng J, Craddock N, Jones IR, Cook EH Jr, Goldman D, Heston LL, Peltonen L, DeLisi LE, Sommer SS. Feng J, et al. Psychiatr Genet. 2001 Mar;11(1):45-8. doi: 10.1097/00041444-200103000-00009. Psychiatr Genet. 2001. PMID: 11409700

8

Elevated frequency of ATM gene missense mutations in breast cancer relative to ethnically matched controls.

Sommer SS, Buzin CH, Jung M, Zheng J, Liu Q, Jeong SJ, Moulds J, Nguyen VQ, Feng J, Bennett WP, Dritschilo A. Sommer SS, et al. Among authors: feng j. Cancer Genet Cytogenet. 2002 Apr 1;134(1):25-32. doi: 10.1016/s0165-4608(01)00594-5. Cancer Genet Cytogenet. 2002. PMID: 11996792

9

Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathy.

Feng J, Yan JY, Buzin CH, Sommer SS, Towbin JA. Feng J, et al. J Am Coll Cardiol. 2002 Sep 18;40(6):1120-4. doi: 10.1016/s0735-1097(02)02126-5. J Am Coll Cardiol. 2002. PMID: 12354438 Free article.

10

Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy.

Feng J, Yan J, Buzin CH, Towbin JA, Sommer SS. Feng J, et al. Mol Genet Metab. 2002 Sep-Oct;77(1-2):119-26. doi: 10.1016/s1096-7192(02)00153-1. Mol Genet Metab. 2002. PMID: 12359139

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