Breen G - Search Results

1

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

Singh T, Kurki MI, Curtis D, Purcell SM, Crooks L, McRae J, Suvisaari J, Chheda H, Blackwood D, Breen G, Pietiläinen O, Gerety SS, Ayub M, Blyth M, Cole T, Collier D, Coomber EL, Craddock N, Daly MJ, Danesh J, DiForti M, Foster A, Freimer NB, Geschwind D, Johnstone M, Joss S, Kirov G, Körkkö J, Kuismin O, Holmans P, Hultman CM, Iyegbe C, Lönnqvist J, Männikkö M, McCarroll SA, McGuffin P, McIntosh AM, McQuillin A, Moilanen JS, Moore C, Murray RM, Newbury-Ecob R, Ouwehand W, Paunio T, Prigmore E, Rees E, Roberts D, Sambrook J, Sklar P, St Clair D, Veijola J, Walters JT, Williams H; Swedish Schizophrenia Study; INTERVAL Study; DDD Study; UK10 K Consortium; Sullivan PF, Hurles ME, O'Donovan MC, Palotie A, Owen MJ, Barrett JC. Singh T, et al. Among authors: breen g. Nat Neurosci. 2016 Apr;19(4):571-7. doi: 10.1038/nn.4267. Epub 2016 Mar 14. Nat Neurosci. 2016. PMID: 26974950 Free PMC article.

2

102T/C polymorphism of serotonin receptor type 2A gene is not associated with schizophrenia in either Chinese or British populations.

He L, Li T, Melville C, Liu S, Feng GY, Gu NF, Fox H, Shaw D, Breen G, Liu X, Sham P, Brown J, Collier D, St Clair D. He L, et al. Among authors: breen g. Am J Med Genet. 1999 Feb 5;88(1):95-8. Am J Med Genet. 1999. PMID: 10050975

3

-141 C del/ins polymorphism of the dopamine receptor 2 gene is associated with schizophrenia in a British population.

Breen G, Brown J, Maude S, Fox H, Collier D, Li T, Arranz M, Shaw D, StClair D. Breen G, et al. Am J Med Genet. 1999 Aug 20;88(4):407-10. doi: 10.1002/(sici)1096-8628(19990820)88:4<407::aid-ajmg19>3.0.co;2-3. Am J Med Genet. 1999. PMID: 10402509

4

Association study of the CACN1A4 (SCA6) triplet repeat and schizophrenia.

Breen G, Fox H, Glen I, Collier D, Shaw D, St Clair D. Breen G, et al. Psychiatr Genet. 1999 Jun;9(2):111-3. doi: 10.1097/00041444-199906000-00012. Psychiatr Genet. 1999. PMID: 10412193

5

Accuracy and sensitivity of DNA pooling with microsatellite repeats using capillary electrophoresis.

Breen G, Sham P, Li T, Shaw D, Collier DA, St Clair D. Breen G, et al. Mol Cell Probes. 1999 Oct;13(5):359-65. doi: 10.1006/mcpr.1999.0259. Mol Cell Probes. 1999. PMID: 10508557

6

No evidence of linkage disequilibrium between a CAG repeat in the SCA1 gene and schizophrenia in Caucasian and Chinese schizophrenic subjects.

Li T, Breen G, Brown J, Liu X, Murray RM, Shaw DJ, Sham PC, St Clair D, Collier DA. Li T, et al. Among authors: breen g. Psychiatr Genet. 1999 Sep;9(3):123-7. doi: 10.1097/00041444-199909000-00002. Psychiatr Genet. 1999. PMID: 10551541

7

Association between angiotensin-converting enzyme gene and late onset Alzheimer's disease in Han chinese.

Yang JD, Feng G, Zhang J, Lin ZX, Shen T, Breen G, St Clair D, He L. Yang JD, et al. Among authors: breen g. Neurosci Lett. 2000 Dec 1;295(1-2):41-4. doi: 10.1016/s0304-3940(00)01591-3. Neurosci Lett. 2000. PMID: 11078932

8

apolipoprotein-E dependent role for the FAS receptor in early onset Alzheimer's disease: finding of a positive association for a polymorphism in the TNFRSF6 gene.

Feuk L, Prince JA, Breen G, Emahazion T, Carothers A, St Clair D, Brookes AJ. Feuk L, et al. Among authors: breen g. Hum Genet. 2000 Oct;107(4):391-6. doi: 10.1007/s004390000383. Hum Genet. 2000. PMID: 11129341

9

The -141C Ins/Del polymorphism of the dopamine D2 receptor gene is not associated with either migraine or Parkinson's disease.

Maude S, Curtin J, Breen G, Collier D, Russell G, Shaw D, Clair DS. Maude S, et al. Among authors: breen g. Psychiatr Genet. 2001 Mar;11(1):49-52. doi: 10.1097/00041444-200103000-00010. Psychiatr Genet. 2001. PMID: 11409701

10

The Tower of Babel? An assessment of the development and state of genetic and SNP technologies.

Breen G, Collier D. Breen G, et al. Psychiatr Genet. 2002 Jun;12(2):59-61. doi: 10.1097/00041444-200206000-00001. Psychiatr Genet. 2002. PMID: 12131756 No abstract available.

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