Year |
Citation |
Score |
2019 |
Ros-Demarize R, Bradley C, Kanne SM, Warren Z, Boan A, Lajonchere C, Park J, Carpenter LA. ASD Symptoms in Toddlers and Preschoolers: An Examination of Sex Differences. Autism Research : Official Journal of the International Society For Autism Research. PMID 31747131 DOI: 10.1002/Aur.2241 |
0.382 |
|
2019 |
McDonnell CG, Bradley CC, Kanne SM, Lajonchere C, Warren Z, Carpenter LA. When Are We Sure? Predictors of Clinician Certainty in the Diagnosis of Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. 49: 1391-1401. PMID 30488151 DOI: 10.1007/S10803-018-3831-3 |
0.363 |
|
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 |
0.327 |
|
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 |
0.404 |
|
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 |
0.388 |
|
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 |
0.399 |
|
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 |
0.41 |
|
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 |
0.374 |
|
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 |
0.368 |
|
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 |
0.375 |
|
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 |
0.413 |
|
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 |
0.344 |
|
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 |
0.418 |
|
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 |
0.37 |
|
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 |
0.446 |
|
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 |
0.345 |
|
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 |
0.374 |
|
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 |
0.43 |
|
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 |
0.359 |
|
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 |
0.409 |
|
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 |
0.499 |
|
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. The American Journal of Psychiatry. 163: 294-6. PMID 16449484 DOI: 10.1176/Appi.Ajp.163.2.294 |
0.407 |
|
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 |
0.302 |
|
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 |
0.359 |
|
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 |
0.315 |
|
1996 |
Lajonchere C, Nortz M, Finger S. Gilles de la Tourette and the discovery of Tourette syndrome: Includes a translation of his 1884 article Archives of Neurology. 53: 567-574. PMID 8660160 DOI: 10.1001/Archneur.1996.00550060111024 |
0.345 |
|
1995 |
Makowski DG, Lajonchere CM, Dicker R, Waternaux C, Smoke N, Koplewicz H, Lev DL. Characterization of thought disorder in early onset schizophrenia Schizophrenia Research. 15: 15. DOI: 10.1016/0920-9964(95)95056-F |
0.34 |
|
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 |
0.329 |
|
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 |
0.385 |
|
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 |
0.319 |
|
Low-probability matches (unlikely to be authored by this person) |
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 |
0.284 |
|
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 |
0.28 |
|
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 |
0.241 |
|
1999 |
Norrsell U, Finger S, Lajonchere C. Cutaneous sensory spots and the "law of specific nerve energies": History and development of ideas Brain Research Bulletin. 48: 457-465. PMID 10372506 DOI: 10.1016/S0361-9230(98)00067-7 |
0.21 |
|
1993 |
Levy D, Dorogusker B, Lajonchere C, Flanagan S, Zitner R, Tartaglini A, Lieberman J, Haimson J, Mendell N. Stability of visual fixation in schizophrenics and normal controls Schizophrenia Research. 9: 162. DOI: 10.1016/0920-9964(93)90302-Y |
0.207 |
|
2024 |
Fu M, Tran T, Eskin E, Lajonchere C, Pasaniuc B, Geschwind DH, Vossel K, Chang TS. Multi-class Modeling Identifies Shared Genetic Risk for Late-onset Epilepsy and Alzheimer's Disease. Medrxiv : the Preprint Server For Health Sciences. PMID 38370677 DOI: 10.1101/2024.02.05.24302353 |
0.16 |
|
2022 |
Zhou W, Kanai M, Wu KH, Rasheed H, Tsuo K, Hirbo JB, Wang Y, Bhattacharya A, Zhao H, Namba S, Surakka I, Wolford BN, Lo Faro V, Lopera-Maya EA, Läll K, ... ... Lajonchere C, et al. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. Cell Genomics. 2: 100192. PMID 36777996 DOI: 10.1016/j.xgen.2022.100192 |
0.155 |
|
2023 |
Johnson R, Ding Y, Bhattacharya A, Knyazev S, Chiu A, Lajonchere C, Geschwind DH, Pasaniuc B. The UCLA ATLAS Community Health Initiative: Promoting precision health research in a diverse biobank. Cell Genomics. 3: 100243. PMID 36777178 DOI: 10.1016/j.xgen.2022.100243 |
0.141 |
|
2022 |
Johnson R, Ding Y, Venkateswaran V, Bhattacharya A, Boulier K, Chiu A, Knyazev S, Schwarz T, Freund M, Zhan L, Burch KS, Caggiano C, Hill B, Rakocz N, Balliu B, ... ... Lajonchere C, et al. Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Genome Medicine. 14: 104. PMID 36085083 DOI: 10.1186/s13073-022-01106-x |
0.113 |
|
2021 |
Lajonchere C, Naeim A, Dry S, Wenger N, Elashoff D, Vangala S, Petruse A, Ariannejad M, Magyar C, Johansen L, Werre G, Kroloff M, Geschwind D. An Integrated, Scalable, Electronic Video Consent Process to Power Precision Health Research: Large, Population-Based, Cohort Implementation and Scalability Study. Journal of Medical Internet Research. 23: e31121. PMID 34889741 DOI: 10.2196/31121 |
0.082 |
|
2021 |
Naeim A, Dry S, Elashoff D, Xie Z, Petruse A, Magyar C, Johansen L, Werre G, Lajonchere C, Wenger N. Electronic Video Consent to Power Precision Health Research: A Pilot Cohort Study. Jmir Formative Research. 5: e29123. PMID 34313247 DOI: 10.2196/29123 |
0.072 |
|
2022 |
Johnson R, Ding Y, Venkateswaran V, Bhattacharya A, Boulier K, Chiu A, Knyazev S, Schwarz T, Freund M, Zhan L, Burch KS, Caggiano C, Hill B, Rakocz N, Balliu B, ... ... Lajonchere C, et al. Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Genome Medicine. 14: 128. PMID 36384576 DOI: 10.1186/s13073-022-01128-5 |
0.069 |
|
2021 |
Naeim A, Dry S, Elashoff D, Xie Z, Petruse A, Magyar C, Johansen L, Werre G, Lajonchere C, Wenger N. Correction: Electronic Video Consent to Power Precision Health Research: A Pilot Cohort Study. Jmir Formative Research. 5: e33891. PMID 34673529 DOI: 10.2196/33891 |
0.057 |
|
2022 |
Stackpole ML, Zeng W, Li S, Liu CC, Zhou Y, He S, Yeh A, Wang Z, Sun F, Li Q, Yuan Z, Yildirim A, Chen PJ, Winograd P, Tran B, ... ... Lajonchere C, et al. Cost-effective methylome sequencing of cell-free DNA for accurately detecting and locating cancer. Nature Communications. 13: 5566. PMID 36175411 DOI: 10.1038/s41467-022-32995-6 |
0.052 |
|
Hide low-probability matches. |