| Year |
Citation |
Score |
| 2014 |
Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, ... ... McInnes LA, et al. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American Journal of Human Genetics. 94: 677-94. PMID 24768552 DOI: 10.1016/J.Ajhg.2014.03.018 |
0.389 |
|
| 2011 |
Sakurai T, Dorr NP, Takahashi N, McInnes LA, Elder GA, Buxbaum JD. Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions. Autism Research : Official Journal of the International Society For Autism Research. 4: 28-39. PMID 21328569 DOI: 10.1002/Aur.169 |
0.358 |
|
| 2010 |
McInnes LA, Nakamine A, Pilorge M, Brandt T, Jiménez González P, Fallas M, Manghi ER, Edelmann L, Glessner J, Hakonarson H, Betancur C, Buxbaum JD. A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region. Molecular Autism. 1: 5. PMID 20678247 DOI: 10.1186/2040-2392-1-5 |
0.335 |
|
| 2008 |
Lauriat TL, Shiue L, Haroutunian V, Verbitsky M, Ares M, Ospina L, McInnes LA. Developmental expression profile of quaking, a candidate gene for schizophrenia, and its target genes in human prefrontal cortex and hippocampus shows regional specificity. Journal of Neuroscience Research. 86: 785-96. PMID 17918747 DOI: 10.1002/Jnr.21534 |
0.748 |
|
| 2008 |
Nakamine A, Ouchanov L, Jiménez P, Manghi ER, Esquivel M, Monge S, Fallas M, Burton BK, Szomju B, Elsea SH, Marshall CR, Scherer SW, McInnes LA. Duplication of 17(p11.2p11.2) in a male child with autism and severe language delay American Journal of Medical Genetics, Part A. 146: 636-643. PMID 17334992 DOI: 10.1002/Ajmg.A.31636 |
0.362 |
|
| 2007 |
Lauriat TL, McInnes LA. EAAT2 regulation and splicing: relevance to psychiatric and neurological disorders. Molecular Psychiatry. 12: 1065-78. PMID 17684493 DOI: 10.1038/sj.mp.4002065 |
0.725 |
|
| 2007 |
Lauriat TL, Schmeidler J, McInnes LA. Early rapid rise in EAAT2 expression follows the period of maximal seizure susceptibility in human brain. Neuroscience Letters. 412: 89-94. PMID 17127000 DOI: 10.1016/J.Neulet.2006.10.037 |
0.721 |
|
| 2007 |
Lauriat TL, Richler E, McInnes LA. A quantitative regional expression profile of EAAT2 known and novel splice variants reopens the question of aberrant EAAT2 splicing in disease. Neurochemistry International. 50: 271-80. PMID 17050039 DOI: 10.1016/J.Neuint.2006.08.014 |
0.732 |
|
| 2007 |
Edelmann L, Prosnitz A, Pardo S, Bhatt J, Cohen N, Lauriat T, Ouchanov L, González PJ, Manghi ER, Bondy P, Esquivel M, Monge S, Delgado MF, Splendore A, Francke U, ... ... McInnes LA, et al. An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism. Journal of Medical Genetics. 44: 136-43. PMID 16971481 DOI: 10.1136/Jmg.2006.044537 |
0.688 |
|
| 2006 |
Lauriat TL, Dracheva S, Kremerskothen J, Duning K, Haroutunian V, Buxbaum JD, Hyde TM, Kleinman JE, McInnes LA. Characterization of KIAA0513, a novel signaling molecule that interacts with modulators of neuroplasticity, apoptosis, and the cytoskeleton. Brain Research. 1121: 1-11. PMID 17010949 DOI: 10.1016/J.Brainres.2006.08.099 |
0.729 |
|
| 2006 |
McInnes LA, Lauriat TL. RNA metabolism and dysmyelination in schizophrenia. Neuroscience and Biobehavioral Reviews. 30: 551-61. PMID 16445981 DOI: 10.1016/J.Neubiorev.2005.10.003 |
0.735 |
|
| 2006 |
Lauriat TL, Dracheva S, Chin B, Schmeidler J, McInnes LA, Haroutunian V. Quantitative analysis of glutamate transporter mRNA expression in prefrontal and primary visual cortex in normal and schizophrenic brain. Neuroscience. 137: 843-51. PMID 16297566 DOI: 10.1016/J.Neuroscience.2005.10.003 |
0.736 |
|
| 2005 |
Ruiz-Rubio M, Mcinnes LA. Serotonin (5-Hydroxytryptamine) and the Etiology of Autism Studies in Natural Products Chemistry. 30: 367-391. DOI: 10.1016/S1572-5995(05)80037-7 |
0.346 |
|
| 2004 |
Hong KS, McInnes LA, Service SK, Song T, Lucas J, Silva S, Fournier E, León P, Molina J, Reus VI, Sandkuijl LA, Freimer NB. Genetic mapping using haplotype and model-free linkage analysis supports previous evidence for a locus predisposing to severe bipolar disorder at 5q31-33. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 125: 83-6. PMID 14755450 DOI: 10.1002/Ajmg.B.20091 |
0.315 |
|
| 2003 |
Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, ... ... McInnes LA, et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. American Journal of Human Genetics. 73: 49-62. PMID 12802785 DOI: 10.1086/376547 |
0.307 |
|
| 2001 |
McInnes LA, Service SK, Reus VI, Barnes G, Charlat O, Jawahar S, Lewitzky S, Yang Q, Duong Q, Spesny M, Araya C, Araya X, Gallegos A, Meza L, Molina J, et al. Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican population. Proceedings of the National Academy of Sciences of the United States of America. 98: 11485-90. PMID 11572994 DOI: 10.1073/Pnas.191519098 |
0.319 |
|
| 1999 |
Escamilla MA, McInnes LA, Spesny M, Reus VI, Service SK, Shimayoshi N, Tyler DJ, Silva S, Molina J, Gallegos A, Meza L, Cruz ML, Batki S, Vinogradov S, Neylan T, et al. Assessing the feasibility of linkage disequilibrium methods for mapping complex traits: an initial screen for bipolar disorder loci on chromosome 18. American Journal of Human Genetics. 64: 1670-8. PMID 10330354 DOI: 10.1086/302400 |
0.303 |
|
| 1998 |
McInnes LA, Reus VI, Freimer NB. Mapping genes for psychiatric disorders and behavioral traits. Current Opinion in Genetics & Development. 8: 287-92. PMID 9690997 DOI: 10.1016/S0959-437X(98)80083-X |
0.313 |
|
| 1996 |
McInnes LA, Escamilla MA, Service SK, Reus VI, Leon P, Silva S, Rojas E, Spesny M, Baharloo S, Blankenship K, Peterson A, Tyler D, Shimayoshi N, Tobey C, Batki S, et al. A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees. Proceedings of the National Academy of Sciences of the United States of America. 93: 13060-5. PMID 8917544 DOI: 10.1073/Pnas.93.23.13060 |
0.315 |
|
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