Yan J - Search Results

1

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: yan 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

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. Psychiatr Genet. 2004 Mar;14(1):57-60. doi: 10.1097/00041444-200403000-00010. Psychiatr Genet. 2004. PMID: 15091318

3

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. Among authors: yan j. 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

4

Vitamin D receptor variants in 192 patients with schizophrenia and other psychiatric diseases.

Yan J, Feng J, Craddock N, Jones IR, Cook EH Jr, Goldman D, Heston LL, Chen J, Burkhart P, Li W, Shibayama A, Sommer SS. Yan J, et al. Neurosci Lett. 2005 May 20-27;380(1-2):37-41. doi: 10.1016/j.neulet.2005.01.018. Epub 2005 Feb 1. Neurosci Lett. 2005. PMID: 15854747

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. Among authors: yan j. 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. 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

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. Psychiatr Genet. 2008 Aug;18(4):204-7. doi: 10.1097/YPG.0b013e3282fb7fe6. Psychiatr Genet. 2008. PMID: 18628683

8

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. Among authors: yan jy. 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.

9

Scanning of estrogen receptor alpha (ERalpha) and thyroid hormone receptor alpha (TRalpha) genes in patients with psychiatric diseases: four missense mutations identified in ERalpha gene.

Feng J, Yan J, Michaud S, Craddock N, Jones IR, Cook EH Jr, Goldman D, Heston LL, Peltonen L, Delisi LE, Sommer SS. Feng J, et al. Among authors: yan j. Am J Med Genet. 2001 May 8;105(4):369-74. doi: 10.1002/ajmg.1364. Am J Med Genet. 2001. PMID: 11378852

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. Among authors: yan j. 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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