Clara M. Lajonchere, Ph.D. - Publications

Affiliations: 
Washington University, Saint Louis, St. Louis, MO 
Area:
Attention and eye movements

28 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Lajonchere CM, Wheeler BY, Valente TW, Kreutzer C, Munson A, Narayanan S, Kazemzadeh A, Cruz R, Martinez I, Schrager SM, Schweitzer L, Chklovski T, Hwang D. Strategies for Disseminating Information on Biomedical Research on Autism to Hispanic Parents. Journal of Autism and Developmental Disorders. PMID 26563948 DOI: 10.1007/s10803-015-2649-5  0.88
2014 Froehlich-Santino W, Londono Tobon A, Cleveland S, Torres A, Phillips J, Cohen B, Torigoe T, Miller J, Fedele A, Collins J, Smith K, Lotspeich L, Croen LA, Ozonoff S, Lajonchere C, et al. Prenatal and perinatal risk factors in a twin study of autism spectrum disorders. Journal of Psychiatric Research. 54: 100-8. PMID 24726638 DOI: 10.1016/j.jpsychires.2014.03.019  0.88
2014 Kas MJ, Glennon JC, Buitelaar J, Ey E, Biemans B, Crawley J, Ring RH, Lajonchere C, Esclassan F, Talpos J, Noldus LP, Burbach JP, Steckler T. Assessing behavioural and cognitive domains of autism spectrum disorders in rodents: current status and future perspectives. Psychopharmacology. 231: 1125-46. PMID 24048469 DOI: 10.1007/s00213-013-3268-5  0.88
2013 Jiang YH, Yuen RK, Jin X, Wang M, Chen N, Wu X, Ju J, Mei J, Shi Y, He M, Wang G, Liang J, Wang Z, Cao D, Carter MT, ... ... Lajonchere C, et al. Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing. American Journal of Human Genetics. 93: 249-63. PMID 23849776 DOI: 10.1016/j.ajhg.2013.06.012  0.88
2013 Froehlich W, Cleveland S, Torres A, Phillips J, Cohen B, Torigoe T, Miller J, Fedele A, Collins J, Smith K, Lotspeich L, Croen LA, Ozonoff S, Lajonchere C, Grether JK, et al. Head circumferences in twins with and without Autism Spectrum Disorders. Journal of Autism and Developmental Disorders. 43: 2026-37. PMID 23321801 DOI: 10.1007/s10803-012-1751-1  0.88
2012 Lajonchere C, Jones N, Coury DL, Perrin JM. Leadership in health care, research, and quality improvement for children and adolescents with autism spectrum disorders: Autism Treatment Network and Autism Intervention Research Network on Physical Health. Pediatrics. 130: S62-8. PMID 23118255 DOI: 10.1542/peds.2012-0900C  0.88
2012 Perrin JM, Coury DL, Jones N, Lajonchere C. The Autism Treatment Network and Autism Intervention Research Network on Physical Health: future directions. Pediatrics. 130: S198-201. PMID 23118252 DOI: 10.1542/peds.2012-0900S  0.88
2012 Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, ... ... Lajonchere CM, et al. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics. 21: 4781-92. PMID 22843504 DOI: 10.1093/hmg/dds301  0.88
2011 Hallmayer J, Cleveland S, Torres A, Phillips J, Cohen B, Torigoe T, Miller J, Fedele A, Collins J, Smith K, Lotspeich L, Croen LA, Ozonoff S, Lajonchere C, Grether JK, et al. Genetic heritability and shared environmental factors among twin pairs with autism. Archives of General Psychiatry. 68: 1095-102. PMID 21727249 DOI: 10.1001/archgenpsychiatry.2011.76  0.88
2011 Pickett J, Xiu E, Tuchman R, Dawson G, Lajonchere C. Mortality in individuals with autism, with and without epilepsy. Journal of Child Neurology. 26: 932-9. PMID 21471551 DOI: 10.1177/0883073811402203  0.88
2010 Lajonchere CM. Changing the landscape of autism research: the autism genetic resource exchange. Neuron. 68: 187-91. PMID 20955925 DOI: 10.1016/j.neuron.2010.10.009  0.88
2010 Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, ... ... Lajonchere CM, et al. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics. 19: 4072-82. PMID 20663923 DOI: 10.1093/hmg/ddq307  0.88
2010 Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, ... ... Lajonchere CM, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 466: 368-72. PMID 20531469 DOI: 10.1038/nature09146  0.88
2009 McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S, Perkins DO, Dickel DE, Kusenda M, Krastoshevsky O, Krause V, Kumar RA, Grozeva D, Malhotra D, Walsh T, ... ... Lajonchere CM, et al. Microduplications of 16p11.2 are associated with schizophrenia. Nature Genetics. 41: 1223-7. PMID 19855392 DOI: 10.1038/ng.474  0.88
2009 Bucan M, Abrahams BS, Wang K, Glessner JT, Herman EI, Sonnenblick LI, Alvarez Retuerto AI, Imielinski M, Hadley D, Bradfield JP, Kim C, Gidaya NB, Lindquist I, Hutman T, Sigman M, ... ... Lajonchere CM, et al. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. Plos Genetics. 5: e1000536. PMID 19557195 DOI: 10.1371/journal.pgen.1000536  0.88
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, ... ... Lajonchere CM, et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature. 459: 528-33. PMID 19404256 DOI: 10.1038/nature07999  0.88
2008 Belmonte MK, Mazziotta JC, Minshew NJ, Evans AC, Courchesne E, Dager SR, Bookheimer SY, Aylward EH, Amaral DG, Cantor RM, Chugani DC, Dale AM, Davatzikos C, Gerig G, Herbert MR, ... ... Lajonchere C, et al. Offering to share: how to put heads together in autism neuroimaging. Journal of Autism and Developmental Disorders. 38: 2-13. PMID 17347882 DOI: 10.1007/s10803-006-0352-2  0.88
2007 Zhao X, Leotta A, Kustanovich V, Lajonchere C, Geschwind DH, Law K, Law P, Qiu S, Lord C, Sebat J, Ye K, Wigler M. A unified genetic theory for sporadic and inherited autism. Proceedings of the National Academy of Sciences of the United States of America. 104: 12831-6. PMID 17652511 DOI: 10.1073/pnas.0705803104  0.88
2007 Cantor RM, Yoon JL, Furr J, Lajonchere CM. Paternal age and autism are associated in a family-based sample. Molecular Psychiatry. 12: 419-21. PMID 17453057 DOI: 10.1038/sj.mp.4001966  0.88
2007 Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, ... ... Lajonchere C, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/ng1985  0.88
2006 Pratt J, Lajonchere CM, Abrams RA. Attentional modulation of the gap effect. Vision Research. 46: 2602-7. PMID 16524610 DOI: 10.1016/j.visres.2006.01.017  0.88
2006 Constantino JN, Lajonchere C, Lutz M, Gray T, Abbacchi A, McKenna K, Singh D, Todd RD. Autistic social impairment in the siblings of children with pervasive developmental disorders American Journal of Psychiatry. 163: 294-296. DOI: 10.1176/appi.ajp.163.2.294  0.88
2000 Levy DL, Lajonchere CM, Dorogusker B, Min D, Lee S, Tartaglini A, Lieberman JA, Mendell NR. Quantitative characterization of eye tracking dysfunction in schizophrenia. Schizophrenia Research. 42: 171-85. PMID 10785576 DOI: 10.1016/S0920-9964(99)00122-X  0.88
1999 Kinney DK, Levy DL, Yurgelun-Todd DA, Lajonchere CM, Holzman PS. Eye-tracking dysfunction and birth-month weather in schizophrenia. Journal of Abnormal Psychology. 108: 359-62. PMID 10369047 DOI: 10.1037/0021-843X.108.2.359  0.88
1997 Makowski D, Waternaux C, Lajonchere CM, Dicker R, Smoke N, Koplewicz H, Min D, Mendell NR, Levy DL. Thought disorder in adolescent-onset schizophrenia. Schizophrenia Research. 23: 147-65. PMID 9061811 DOI: 10.1016/S0920-9964(96)00097-7  0.88
1994 Kinney DK, Levy DL, Yurgelun-Todd DA, Medoff D, LaJonchere CM, Radford-Paregol M. Season of birth and obstetrical complications in schizophrenics. Journal of Psychiatric Research. 28: 499-509. PMID 7699609 DOI: 10.1016/0022-3956(94)90040-X  0.88
1993 Kinney DK, Yurgelun-Todd DA, Levy DL, Medoff D, Lajonchere CM, Radford-Paregol M. Obstetrical complications in patients with bipolar disorder and their siblings. Psychiatry Research. 48: 47-56. PMID 8416018 DOI: 10.1016/0165-1781(93)90112-T  0.88
1992 Matthysse S, Levy DL, Kinney D, Deutsch C, Lajonchere C, Yurgelun-Todd D, Woods B, Holzman PS. Gene expression in mental illness: a navigation chart to future progress. Journal of Psychiatric Research. 26: 461-73. PMID 1491362 DOI: 10.1016/0022-3956(92)90046-Q  0.88
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