| Year |
Citation |
Score |
| Low-probability matches (unlikely to be authored by this person) |
| 2010 |
Buresh JS, Woodward A, Brune CW. The Roots of Verbs in Prelinguistic Action Knowledge Action Meets Word: How Children Learn Verbs. DOI: 10.1093/acprof:oso/9780195170009.003.0009 |
0.289 |
|
| 2007 |
Brune CW, Woodward AL. Social cognition and social responsiveness in 10-month-old infants Journal of Cognition and Development. 8: 133-158. DOI: 10.1080/15248370701202331 |
0.267 |
|
| 2009 |
Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, ... ... Brune CW, et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature. 459: 528-33. PMID 19404256 DOI: 10.1038/Nature07999 |
0.136 |
|
| 2008 |
Brune CW, Korvatska E, Allen-Brady K, Cook EH, Dawson G, Devlin B, Estes A, Hennelly M, Hyman SL, McMahon WM, Munson J, Rodier PM, Schellenberg GD, Stodgell CJ, Coon H. Heterogeneous association between engrailed-2 and autism in the CPEA network. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 187-93. PMID 17948868 DOI: 10.1002/Ajmg.B.30585 |
0.122 |
|
| 2010 |
Owley T, Brune CW, Salt J, Walton L, Guter S, Ayuyao N, Gibbons RD, Leventhal BL, Cook EH. A pharmacogenetic study of escitalopram in autism spectrum disorders. Autism Research : Official Journal of the International Society For Autism Research. 3: 1-7. PMID 20020537 DOI: 10.1002/aur.109 |
0.109 |
|
| 2007 |
Jacob S, Brune CW, Carter CS, Leventhal BL, Lord C, Cook EH. Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism. Neuroscience Letters. 417: 6-9. PMID 17383819 DOI: 10.1016/J.Neulet.2007.02.001 |
0.092 |
|
| 2008 |
Christian SL, Brune CW, Sudi J, Kumar RA, Liu S, Karamohamed S, Badner JA, Matsui S, Conroy J, McQuaid D, Gergel J, Hatchwell E, Gilliam TC, Gershon ES, Nowak NJ, et al. Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biological Psychiatry. 63: 1111-7. PMID 18374305 DOI: 10.1016/J.Biopsych.2008.01.009 |
0.09 |
|
| 2006 |
Brune CW, Kim SJ, Salt J, Leventhal BL, Lord C, Cook EH. 5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism. The American Journal of Psychiatry. 163: 2148-56. PMID 17151167 DOI: 10.1176/Ajp.2006.163.12.2148 |
0.087 |
|
| 2011 |
Kistner-Griffin E, Brune CW, Davis LK, Sutcliffe JS, Cox NJ, Cook EH. Parent-of-origin effects of the serotonin transporter gene associated with autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 139-44. PMID 21302342 DOI: 10.1002/Ajmg.B.31146 |
0.087 |
|
| 2008 |
Kim SJ, Brune CW, Kistner EO, Christian SL, Courchesne EH, Cox NJ, Cook EH. Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1116-25. PMID 18361419 DOI: 10.1002/Ajmg.B.30733 |
0.087 |
|
| 2009 |
Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature. 459: 569-73. PMID 19404257 DOI: 10.1038/Nature07953 |
0.082 |
|
| 2009 |
Weiss LA, Arking DE, Daly MJ, Chakravarti A, Brune CW, West K, O'Connor A, Hilton G, Tomlinson RL, West AB, Cook EH, Green T, Chang SC, Gabriel S, Gates C, et al. A genome-wide linkage and association scan reveals novel loci for autism Nature. 461: 802-808. PMID 19812673 DOI: 10.1038/Nature08490 |
0.073 |
|
| 2011 |
Delahanty RJ, Kang JQ, Brune CW, Kistner EO, Courchesne E, Cox NJ, Cook EH, Macdonald RL, Sutcliffe JS. Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism. Molecular Psychiatry. 16: 86-96. PMID 19935738 DOI: 10.1038/Mp.2009.118 |
0.073 |
|
| 2008 |
Kumar RA, KaraMohamed S, Sudi J, Conrad DF, Brune C, Badner JA, Gilliam TC, Nowak NJ, Cook EH, Dobyns WB, Christian SL. Recurrent 16p11.2 microdeletions in autism. Human Molecular Genetics. 17: 628-38. PMID 18156158 DOI: 10.1093/Hmg/Ddm376 |
0.064 |
|
| 2009 |
Kumar RA, Marshall CR, Badner JA, Babatz TD, Mukamel Z, Aldinger KA, Sudi J, Brune CW, Goh G, Karamohamed S, Sutcliffe JS, Cook EH, Geschwind DH, Dobyns WB, Scherer SW, et al. Association and mutation analyses of 16p11.2 autism candidate genes. Plos One. 4: e4582. PMID 19242545 DOI: 10.1371/Journal.Pone.0004582 |
0.063 |
|
| 2010 |
Kumar RA, Sudi J, Babatz TD, Brune CW, Oswald D, Yen M, Nowak NJ, Cook EH, Christian SL, Dobyns WB. A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism. Journal of Medical Genetics. 47: 81-90. PMID 19546099 DOI: 10.1136/Jmg.2008.065821 |
0.063 |
|
| 2008 |
Brune CW, Kim SJ, Hanna GL, Courchesne E, Lord C, Leventhal BL, Cook EH. Family-Based Association Testing of OCD-associated SNPs of SLC1A1 in an autism sample. Autism Research : Official Journal of the International Society For Autism Research. 1: 108-13. PMID 19360657 DOI: 10.1002/Aur.11 |
0.061 |
|
| 2008 |
Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH, Chakravarti A. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. American Journal of Human Genetics. 82: 160-4. PMID 18179894 DOI: 10.1016/J.Ajhg.2007.09.015 |
0.059 |
|
| 2011 |
Jacob S, Brune CW, Badner JA, Ernstrom K, Courchesne E, Lord C, Leventhal BL, Cook EH, Kim SJ. Family-based association testing of glutamate transporter genes in autism. Psychiatric Genetics. 21: 212-3. PMID 21085054 DOI: 10.1097/Ypg.0B013E328341A323 |
0.048 |
|
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