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Աուտիզմի առաջացման պատճառներ (Armenian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Աուտիզմի առաջացման պատճառներ" in Armenian language version.

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  • McPartland, James C.; Law, Karen; Dawson, Geraldine (2015 թ․ օգոստոսի 26). Autism Spectrum Disorder. էջեր 124–130. doi:10.1016/B978-0-12-397045-9.00230-5. ISBN 9780123977533. {{cite book}}: |work= ignored (օգնություն)
  • Hallmayer, Joachim (2011 թ․ նոյեմբերի 1). «Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism». Archives of General Psychiatry. 68 (11): 1095–1102. doi:10.1001/archgenpsychiatry.2011.76. PMC 4440679. PMID 21727249.
  • Ronald, Angelica; Hoekstra, Rosa A. (2011 թ․ ապրիլ). «Autism spectrum disorders and autistic traits: A decade of new twin studies». American Journal of Medical Genetics Part B. 156 (3): 255–274. doi:10.1002/ajmg.b.31159.
  • Sebat, J.; Lakshmi, B.; Malhotra, D.; Troge, J.; Lese-Martin, C.; Walsh, T.; Yamrom, B.; Yoon, S.; Krasnitz, A. (2007 թ․ ապրիլի 20). «Strong Association of De Novo Copy Number Mutations with Autism». Science. 316 (5823): 445–449. doi:10.1126/science.1138659. PMC 2993504. PMID 17363630.
  • Uher, R (2009 թ․ օգոստոսի 25). «The role of genetic variation in the causation of mental illness: an evolution-informed framework». Molecular Psychiatry. 14 (12): 1072–1082. doi:10.1038/mp.2009.85. PMID 19704409.
  • Hultman, C M; Sandin, S; Levine, S Z; Lichtenstein, P; Reichenberg, A (2010 թ․ նոյեմբերի 30). «Advancing paternal age and risk of autism: new evidence from a population-based study and a meta-analysis of epidemiological studies». Molecular Psychiatry. 16 (12): 1203–1212. doi:10.1038/mp.2010.121. PMID 21116277.
  • Kong, Augustine; Frigge, Michael L.; Masson, Gisli; Besenbacher, Soren; Sulem, Patrick; Magnusson, Gisli; Gudjonsson, Sigurjon A.; Sigurdsson, Asgeir; Jonasdottir, Aslaug (2012 թ․ օգոստոսի 22). «Rate of de novo mutations and the importance of father's age to disease risk». Nature. 488 (7412): 471–475. doi:10.1038/nature11396. PMC 3548427. PMID 22914163.
  • Hatton, Deborah D.; Sideris, John; Skinner, Martie; Mankowski, Jean; Bailey, Donald B.; Roberts, Jane; Mirrett, Penny (2006 թ․ սեպտեմբերի 1). «Autistic behavior in children with fragile X syndrome: Prevalence, stability, and the impact of FMRP». American Journal of Medical Genetics Part A. 140A (17): 1804–1813. doi:10.1002/ajmg.a.31286. PMID 16700053.
  • Zoghbi, Huda Y.; Amir, Ruthie E.; Van den Veyver, Ignatia B.; Wan, Mimi; Tran, Charles Q.; Francke, Uta (1999 թ․ հոկտեմբերի 1). «Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2». Nature Genetics. 23 (2): 185–188. doi:10.1038/13810. PMID 10508514.
  • Sebat, J. (2004 թ․ հուլիսի 23). «Large-Scale Copy Number Polymorphism in the Human Genome». Science. 305 (5683): 525–528. doi:10.1126/science.1098918. PMID 15273396.
  • Iafrate, A John; Feuk, Lars; Rivera, Miguel N; Listewnik, Marc L; Donahoe, Patricia K; Qi, Ying; Scherer, Stephen W; Lee, Charles (2004 թ․ օգոստոսի 1). «Detection of large-scale variation in the human genome». Nature Genetics. 36 (9): 949–951. doi:10.1038/ng1416. PMID 15286789.
  • Pinto, Dalila; Delaby, Elsa; Merico, Daniele; Barbosa, Mafalda; Merikangas, Alison; Klei, Lambertus; Thiruvahindrapuram, Bhooma; Xu, Xiao; Ziman, Robert (2014 թ․ մայիս). «Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders». The American Journal of Human Genetics. 94 (5): 677–694. doi:10.1016/j.ajhg.2014.03.018. PMC 4067558. PMID 24768552. {{cite journal}}: Invalid |display-authors=29 (օգնություն)
  • Levy, Dan; Ronemus, Michael; Yamrom, Boris; Lee, Yoon-ha; Leotta, Anthony; Kendall, Jude; Marks, Steven; Lakshmi, B.; Pai, Deepa (2011 թ․ հունիս). «Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders». Neuron. 70 (5): 886–897. doi:10.1016/j.neuron.2011.05.015. PMID 21658582.
  • Sanders, Stephan J.; Ercan-Sencicek, A. Gulhan; Hus, Vanessa; Luo, Rui; Murtha, Michael T.; Moreno-De-Luca, Daniel; Chu, Su H.; Moreau, Michael P.; Gupta, Abha R. (2011 թ․ հունիս). «Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism». Neuron. 70 (5): 863–885. doi:10.1016/j.neuron.2011.05.002. PMC 3939065. PMID 21658581.
  • Sanders, Stephan J.; Ercan-Sencicek, A. Gulhan; Hus, Vanessa; Luo, Rui; Murtha, Michael T.; Moreno-De-Luca, Daniel; Chu, Su H.; Moreau, Michael P.; Gupta, Abha R.; Thomson, Susanne A.; Mason, Christopher E.; Bilguvar, Kaya; Celestino-Soper, Patricia B.S.; Choi, Murim; Crawford, Emily L.; Davis, Lea; Davis Wright, Nicole R.; Dhodapkar, Rahul M.; DiCola, Michael; DiLullo, Nicholas M.; Fernandez, Thomas V.; Fielding-Singh, Vikram; Fishman, Daniel O.; Frahm, Stephanie; Garagaloyan, Rouben; Goh, Gerald S.; Kammela, Sindhuja; Klei, Lambertus; Lowe, Jennifer K.; Lund, Sabata C.; McGrew, Anna D.; Meyer, Kyle A.; Moffat, William J.; Murdoch, John D.; O'Roak, Brian J.; Ober, Gordon T.; Pottenger, Rebecca S.; Raubeson, Melanie J.; Song, Youeun; Wang, Qi; Yaspan, Brian L.; Yu, Timothy W.; Yurkiewicz, Ilana R.; Beaudet, Arthur L.; Cantor, Rita M.; Curland, Martin; Grice, Dorothy E.; Günel, Murat; Lifton, Richard P.; Mane, Shrikant M.; Martin, Donna M.; Shaw, Chad A.; Sheldon, Michael; Tischfield, Jay A.; Walsh, Christopher A.; Morrow, Eric M.; Ledbetter, David H.; Fombonne, Eric; Lord, Catherine; Martin, Christa Lese; Brooks, Andrew I.; Sutcliffe, James S.; Cook, Edwin H.; Geschwind, Daniel; Roeder, Kathryn; Devlin, Bernie; State, Matthew W. (2011 թ․ հունիս). «Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism». Neuron. 70 (5): 863–885. doi:10.1016/j.neuron.2011.05.002. PMC 3939065. PMID 21658581.
  • Brandler, William M.; Antaki, Danny; Gujral, Madhusudan; Noor, Amina; Rosanio, Gabriel; Chapman, Timothy R.; Barrera, Daniel J.; Lin, Guan Ning; Malhotra, Dheeraj; Watts, Amanda C.; Wong, Lawrence C.; Estabillo, Jasper A.; Gadomski, Therese E.; Hong, Oanh; Fajardo, Karin V. Fuentes; Bhandari, Abhishek; Owen, Renius; Baughn, Michael; Yuan, Jeffrey; Solomon, Terry; Moyzis, Alexandra G.; Maile, Michelle S.; Sanders, Stephan J.; Reiner, Gail E.; Vaux, Keith K.; Strom, Charles M.; Zhang, Kang; Muotri, Alysson R.; Akshoomoff, Natacha; Leal, Suzanne M.; Pierce, Karen; Courchesne, Eric; Iakoucheva, Lilia M.; Corsello, Christina; Sebat, Jonathan (2016 թ․ մարտ). «Frequency and Complexity of De Novo Structural Mutation in Autism». The American Journal of Human Genetics. 98 (4): 667–679. doi:10.1016/j.ajhg.2016.02.018. PMC 4833290. PMID 27018473.
  • Iossifov, Ivan; Ronemus, Michael; Levy, Dan; Wang, Zihua; Hakker, Inessa; Rosenbaum, Julie; Yamrom, Boris; Lee, Yoon-ha; Narzisi, Giuseppe; Leotta, Anthony; Kendall, Jude; Grabowska, Ewa; Ma, Beicong; Marks, Steven; Rodgers, Linda; Stepansky, Asya; Troge, Jennifer; Andrews, Peter; Bekritsky, Mitchell; Pradhan, Kith; Ghiban, Elena; Kramer, Melissa; Parla, Jennifer; Demeter, Ryan; Fulton, Lucinda L.; Fulton, Robert S.; Magrini, Vincent J.; Ye, Kenny; Darnell, Jennifer C.; Darnell, Robert B.; Mardis, Elaine R.; Wilson, Richard K.; Schatz, Michael C.; McCombie, W. Richard; Wigler, Michael (2012 թ․ ապրիլ). «De Novo Gene Disruptions in Children on the Autistic Spectrum». Neuron. 74 (2): 285–299. doi:10.1016/j.neuron.2012.04.009. PMC 3619976. PMID 22542183.
  • De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Ercument Cicek, A.; Kou, Yan; Liu, Li; Fromer, Menachem; Walker, Susan; Singh, Tarjinder; Klei, Lambertus; Kosmicki, Jack; Fu, Shih-Chen; Aleksic, Branko; Biscaldi, Monica; Bolton, Patrick F.; Brownfeld, Jessica M.; Cai, Jinlu; Campbell, Nicholas G.; Carracedo, Angel; Chahrour, Maria H.; Chiocchetti, Andreas G.; Coon, Hilary; Crawford, Emily L.; Crooks, Lucy; Curran, Sarah R.; Dawson, Geraldine; Duketis, Eftichia; Fernandez, Bridget A.; Gallagher, Louise; Geller, Evan; Guter, Stephen J.; Sean Hill, R.; Ionita-Laza, Iuliana; Jimenez Gonzalez, Patricia; Kilpinen, Helena; Klauck, Sabine M.; Kolevzon, Alexander; Lee, Irene; Lei, Jing; Lehtimäki, Terho; Lin, Chiao-Feng; Ma’ayan, Avi; Marshall, Christian R.; McInnes, Alison L.; Neale, Benjamin; Owen, Michael J.; Ozaki, Norio; Parellada, Mara; Parr, Jeremy R.; Purcell, Shaun; Puura, Kaija; Rajagopalan, Deepthi; Rehnström, Karola; Reichenberg, Abraham; Sabo, Aniko; Sachse, Michael; Sanders, Stephan J.; Schafer, Chad; Schulte-Rüther, Martin; Skuse, David; Stevens, Christine; Szatmari, Peter; Tammimies, Kristiina; Valladares, Otto; Voran, Annette; Wang, Li-San; Weiss, Lauren A.; Jeremy Willsey, A.; Yu, Timothy W.; Yuen, Ryan K. C.; Cook, Edwin H.; Freitag, Christine M.; Gill, Michael; Hultman, Christina M.; Lehner, Thomas; Palotie, Aarno; Schellenberg, Gerard D.; Sklar, Pamela; State, Matthew W.; Sutcliffe, James S.; Walsh, Christopher A.; Scherer, Stephen W.; Zwick, Michael E.; Barrett, Jeffrey C.; Cutler, David J.; Roeder, Kathryn; Devlin, Bernie; Daly, Mark J.; Buxbaum, Joseph D. (2014 թ․ հոկտեմբերի 29). «Synaptic, transcriptional and chromatin genes disrupted in autism». Nature. 515 (7526): 209–215. doi:10.1038/nature13772. PMC 4402723. PMID 25363760.
  • Iossifov, Ivan; O’Roak, Brian J.; Sanders, Stephan J.; Ronemus, Michael; Krumm, Niklas; Levy, Dan; Stessman, Holly A.; Witherspoon, Kali T.; Vives, Laura; Patterson, Karynne E.; Smith, Joshua D.; Paeper, Bryan; Nickerson, Deborah A.; Dea, Jeanselle; Dong, Shan; Gonzalez, Luis E.; Mandell, Jeffrey D.; Mane, Shrikant M.; Murtha, Michael T.; Sullivan, Catherine A.; Walker, Michael F.; Waqar, Zainulabedin; Wei, Liping; Willsey, A. Jeremy; Yamrom, Boris; Lee, Yoon-ha; Grabowska, Ewa; Dalkic, Ertugrul; Wang, Zihua; Marks, Steven; Andrews, Peter; Leotta, Anthony; Kendall, Jude; Hakker, Inessa; Rosenbaum, Julie; Ma, Beicong; Rodgers, Linda; Troge, Jennifer; Narzisi, Giuseppe; Yoon, Seungtai; Schatz, Michael C.; Ye, Kenny; McCombie, W. Richard; Shendure, Jay; Eichler, Evan E.; State, Matthew W.; Wigler, Michael (2014 թ․ հոկտեմբերի 29). «The contribution of de novo coding mutations to autism spectrum disorder». Nature. 515 (7526): 216–221. doi:10.1038/nature13908. PMC 4313871. PMID 25363768.
  • Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma’ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San; Makarov, Vladimir; Polak, Paz; Yoon, Seungtai; Maguire, Jared; Crawford, Emily L.; Campbell, Nicholas G.; Geller, Evan T.; Valladares, Otto; Schafer, Chad; Liu, Han; Zhao, Tuo; Cai, Guiqing; Lihm, Jayon; Dannenfelser, Ruth; Jabado, Omar; Peralta, Zuleyma; Nagaswamy, Uma; Muzny, Donna; Reid, Jeffrey G.; Newsham, Irene; Wu, Yuanqing; Lewis, Lora; Han, Yi; Voight, Benjamin F.; Lim, Elaine; Rossin, Elizabeth; Kirby, Andrew; Flannick, Jason; Fromer, Menachem; Shakir, Khalid; Fennell, Tim; Garimella, Kiran; Banks, Eric; Poplin, Ryan; Gabriel, Stacey; DePristo, Mark; Wimbish, Jack R.; Boone, Braden E.; Levy, Shawn E.; Betancur, Catalina; Sunyaev, Shamil; Boerwinkle, Eric; Buxbaum, Joseph D.; Cook Jr, Edwin H.; Devlin, Bernie; Gibbs, Richard A.; Roeder, Kathryn; Schellenberg, Gerard D.; Sutcliffe, James S.; Daly, Mark J. (2012 թ․ ապրիլի 4). «Patterns and rates of exonic de novo mutations in autism spectrum disorders». Nature. 485 (7397): 242–245. doi:10.1038/nature11011. PMC 3613847. PMID 22495311.
  • Sanders, Stephan J.; Murtha, Michael T.; Gupta, Abha R.; Murdoch, John D.; Raubeson, Melanie J.; Willsey, A. Jeremy; Ercan-Sencicek, A. Gulhan; DiLullo, Nicholas M.; Parikshak, Neelroop N.; Stein, Jason L.; Walker, Michael F.; Ober, Gordon T.; Teran, Nicole A.; Song, Youeun; El-Fishawy, Paul; Murtha, Ryan C.; Choi, Murim; Overton, John D.; Bjornson, Robert D.; Carriero, Nicholas J.; Meyer, Kyle A.; Bilguvar, Kaya; Mane, Shrikant M.; Šestan, Nenad; Lifton, Richard P.; Günel, Murat; Roeder, Kathryn; Geschwind, Daniel H.; Devlin, Bernie; State, Matthew W. (2012 թ․ ապրիլի 4). «De novo mutations revealed by whole-exome sequencing are strongly associated with autism». Nature. 485 (7397): 237–241. doi:10.1038/nature10945. PMC 3667984. PMID 22495306.
  • O’Roak, Brian J.; Vives, Laura; Girirajan, Santhosh; Karakoc, Emre; Krumm, Niklas; Coe, Bradley P.; Levy, Roie; Ko, Arthur; Lee, Choli; Smith, Joshua D.; Turner, Emily H.; Stanaway, Ian B.; Vernot, Benjamin; Malig, Maika; Baker, Carl; Reilly, Beau; Akey, Joshua M.; Borenstein, Elhanan; Rieder, Mark J.; Nickerson, Deborah A.; Bernier, Raphael; Shendure, Jay; Eichler, Evan E. (2012 թ․ ապրիլի 4). «Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations». Nature. 485 (7397): 246–250. doi:10.1038/nature10989. PMC 3350576. PMID 22495309.
  • Ronemus, Michael; Iossifov, Ivan; Levy, Dan; Wigler, Michael (2014 թ․ հունվարի 16). «The role of de novo mutations in the genetics of autism spectrum disorders». Nature Reviews Genetics. 15 (2): 133–141. doi:10.1038/nrg3585. PMID 24430941.
  • Betancur, Catalina (2011 թ․ մարտ). «Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting». Brain Research. 1380: 42–77. doi:10.1016/j.brainres.2010.11.078. PMID 21129364.
  • Stefansson, Hreinn; Meyer-Lindenberg, Andreas; Steinberg, Stacy; Magnusdottir, Brynja; Morgen, Katrin; Arnarsdottir, Sunna; Bjornsdottir, Gyda; Walters, G. Bragi; Jonsdottir, Gudrun A.; Doyle, Orla M.; Tost, Heike; Grimm, Oliver; Kristjansdottir, Solveig; Snorrason, Heimir; Davidsdottir, Solveig R.; Gudmundsson, Larus J.; Jonsson, Gudbjorn F.; Stefansdottir, Berglind; Helgadottir, Isafold; Haraldsson, Magnus; Jonsdottir, Birna; Thygesen, Johan H.; Schwarz, Adam J.; Didriksen, Michael; Stensbøl, Tine B.; Brammer, Michael; Kapur, Shitij; Halldorsson, Jonas G.; Hreidarsson, Stefan; Saemundsen, Evald; Sigurdsson, Engilbert; Stefansson, Kari (2013 թ․ դեկտեմբերի 18). «CNVs conferring risk of autism or schizophrenia affect cognition in controls». Nature. 505 (7483): 361–366. doi:10.1038/nature12818. PMID 24352232.
  • Shinawi, M.; Liu, P.; Kang, S. H. L.; Shen, J.; Belmont, J. W.; Scott, D. A.; Probst, F. J.; Craigen, W. J.; Graham, B. H.; Pursley, A.; Clark, G.; Lee, J.; Proud, M.; Stocco, A.; Rodriguez, D. L.; Kozel, B. A.; Sparagana, S.; Roeder, E. R.; McGrew, S. G.; Kurczynski, T. W.; Allison, L. J.; Amato, S.; Savage, S.; Patel, A.; Stankiewicz, P.; Beaudet, A. L.; Cheung, S. W.; Lupski, J. R. (2009 թ․ նոյեմբերի 12). «Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size». Journal of Medical Genetics. 47 (5): 332–341. doi:10.1136/jmg.2009.073015. PMC 3158566. PMID 19914906.
  • Brandler, William M.; Sebat, Jonathan (2015 թ․ հունվարի 14). «From De Novo Mutations to Personalized Therapeutic Interventions in Autism». Annual Review of Medicine. 66 (1): 487–507. doi:10.1146/annurev-med-091113-024550. PMID 25587659.
  • «Pathophysiology of autism spectrum disorders: revisiting gastrointestinal involvement and immune imbalance». World J Gastroenterol (Review). 20 (29): 9942–51. 2014. doi:10.3748/wjg.v20.i29.9942. PMC 4123375. PMID 25110424.{{cite journal}}: CS1 սպաս․ չպիտակված ազատ DOI (link)
  • «Neurodevelopment: The Impact of Nutrition and Inflammation During Preconception and Pregnancy in Low-Resource Settings». Pediatrics (Review). 139 (Suppl 1): S38–S49. 2017. doi:10.1542/peds.2016-2828F. PMID 28562247.

europa.eu

emea.europa.eu

fda.gov

globalnews.ca

inserm.fr

hal.inserm.fr

iom.edu

jleukbio.org

livescience.com

mmrthefacts.nhs.uk

nih.gov

ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov

  • Hallmayer, Joachim (2011 թ․ նոյեմբերի 1). «Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism». Archives of General Psychiatry. 68 (11): 1095–1102. doi:10.1001/archgenpsychiatry.2011.76. PMC 4440679. PMID 21727249.
  • Sebat, J.; Lakshmi, B.; Malhotra, D.; Troge, J.; Lese-Martin, C.; Walsh, T.; Yamrom, B.; Yoon, S.; Krasnitz, A. (2007 թ․ ապրիլի 20). «Strong Association of De Novo Copy Number Mutations with Autism». Science. 316 (5823): 445–449. doi:10.1126/science.1138659. PMC 2993504. PMID 17363630.
  • Uher, R (2009 թ․ օգոստոսի 25). «The role of genetic variation in the causation of mental illness: an evolution-informed framework». Molecular Psychiatry. 14 (12): 1072–1082. doi:10.1038/mp.2009.85. PMID 19704409.
  • Hultman, C M; Sandin, S; Levine, S Z; Lichtenstein, P; Reichenberg, A (2010 թ․ նոյեմբերի 30). «Advancing paternal age and risk of autism: new evidence from a population-based study and a meta-analysis of epidemiological studies». Molecular Psychiatry. 16 (12): 1203–1212. doi:10.1038/mp.2010.121. PMID 21116277.
  • Kong, Augustine; Frigge, Michael L.; Masson, Gisli; Besenbacher, Soren; Sulem, Patrick; Magnusson, Gisli; Gudjonsson, Sigurjon A.; Sigurdsson, Asgeir; Jonasdottir, Aslaug (2012 թ․ օգոստոսի 22). «Rate of de novo mutations and the importance of father's age to disease risk». Nature. 488 (7412): 471–475. doi:10.1038/nature11396. PMC 3548427. PMID 22914163.
  • Hatton, Deborah D.; Sideris, John; Skinner, Martie; Mankowski, Jean; Bailey, Donald B.; Roberts, Jane; Mirrett, Penny (2006 թ․ սեպտեմբերի 1). «Autistic behavior in children with fragile X syndrome: Prevalence, stability, and the impact of FMRP». American Journal of Medical Genetics Part A. 140A (17): 1804–1813. doi:10.1002/ajmg.a.31286. PMID 16700053.
  • Zoghbi, Huda Y.; Amir, Ruthie E.; Van den Veyver, Ignatia B.; Wan, Mimi; Tran, Charles Q.; Francke, Uta (1999 թ․ հոկտեմբերի 1). «Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2». Nature Genetics. 23 (2): 185–188. doi:10.1038/13810. PMID 10508514.
  • Sebat, J. (2004 թ․ հուլիսի 23). «Large-Scale Copy Number Polymorphism in the Human Genome». Science. 305 (5683): 525–528. doi:10.1126/science.1098918. PMID 15273396.
  • Iafrate, A John; Feuk, Lars; Rivera, Miguel N; Listewnik, Marc L; Donahoe, Patricia K; Qi, Ying; Scherer, Stephen W; Lee, Charles (2004 թ․ օգոստոսի 1). «Detection of large-scale variation in the human genome». Nature Genetics. 36 (9): 949–951. doi:10.1038/ng1416. PMID 15286789.
  • Pinto, Dalila; Delaby, Elsa; Merico, Daniele; Barbosa, Mafalda; Merikangas, Alison; Klei, Lambertus; Thiruvahindrapuram, Bhooma; Xu, Xiao; Ziman, Robert (2014 թ․ մայիս). «Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders». The American Journal of Human Genetics. 94 (5): 677–694. doi:10.1016/j.ajhg.2014.03.018. PMC 4067558. PMID 24768552. {{cite journal}}: Invalid |display-authors=29 (օգնություն)
  • Levy, Dan; Ronemus, Michael; Yamrom, Boris; Lee, Yoon-ha; Leotta, Anthony; Kendall, Jude; Marks, Steven; Lakshmi, B.; Pai, Deepa (2011 թ․ հունիս). «Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders». Neuron. 70 (5): 886–897. doi:10.1016/j.neuron.2011.05.015. PMID 21658582.
  • Sanders, Stephan J.; Ercan-Sencicek, A. Gulhan; Hus, Vanessa; Luo, Rui; Murtha, Michael T.; Moreno-De-Luca, Daniel; Chu, Su H.; Moreau, Michael P.; Gupta, Abha R. (2011 թ․ հունիս). «Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism». Neuron. 70 (5): 863–885. doi:10.1016/j.neuron.2011.05.002. PMC 3939065. PMID 21658581.
  • Sanders, Stephan J.; Ercan-Sencicek, A. Gulhan; Hus, Vanessa; Luo, Rui; Murtha, Michael T.; Moreno-De-Luca, Daniel; Chu, Su H.; Moreau, Michael P.; Gupta, Abha R.; Thomson, Susanne A.; Mason, Christopher E.; Bilguvar, Kaya; Celestino-Soper, Patricia B.S.; Choi, Murim; Crawford, Emily L.; Davis, Lea; Davis Wright, Nicole R.; Dhodapkar, Rahul M.; DiCola, Michael; DiLullo, Nicholas M.; Fernandez, Thomas V.; Fielding-Singh, Vikram; Fishman, Daniel O.; Frahm, Stephanie; Garagaloyan, Rouben; Goh, Gerald S.; Kammela, Sindhuja; Klei, Lambertus; Lowe, Jennifer K.; Lund, Sabata C.; McGrew, Anna D.; Meyer, Kyle A.; Moffat, William J.; Murdoch, John D.; O'Roak, Brian J.; Ober, Gordon T.; Pottenger, Rebecca S.; Raubeson, Melanie J.; Song, Youeun; Wang, Qi; Yaspan, Brian L.; Yu, Timothy W.; Yurkiewicz, Ilana R.; Beaudet, Arthur L.; Cantor, Rita M.; Curland, Martin; Grice, Dorothy E.; Günel, Murat; Lifton, Richard P.; Mane, Shrikant M.; Martin, Donna M.; Shaw, Chad A.; Sheldon, Michael; Tischfield, Jay A.; Walsh, Christopher A.; Morrow, Eric M.; Ledbetter, David H.; Fombonne, Eric; Lord, Catherine; Martin, Christa Lese; Brooks, Andrew I.; Sutcliffe, James S.; Cook, Edwin H.; Geschwind, Daniel; Roeder, Kathryn; Devlin, Bernie; State, Matthew W. (2011 թ․ հունիս). «Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism». Neuron. 70 (5): 863–885. doi:10.1016/j.neuron.2011.05.002. PMC 3939065. PMID 21658581.
  • Brandler, William M.; Antaki, Danny; Gujral, Madhusudan; Noor, Amina; Rosanio, Gabriel; Chapman, Timothy R.; Barrera, Daniel J.; Lin, Guan Ning; Malhotra, Dheeraj; Watts, Amanda C.; Wong, Lawrence C.; Estabillo, Jasper A.; Gadomski, Therese E.; Hong, Oanh; Fajardo, Karin V. Fuentes; Bhandari, Abhishek; Owen, Renius; Baughn, Michael; Yuan, Jeffrey; Solomon, Terry; Moyzis, Alexandra G.; Maile, Michelle S.; Sanders, Stephan J.; Reiner, Gail E.; Vaux, Keith K.; Strom, Charles M.; Zhang, Kang; Muotri, Alysson R.; Akshoomoff, Natacha; Leal, Suzanne M.; Pierce, Karen; Courchesne, Eric; Iakoucheva, Lilia M.; Corsello, Christina; Sebat, Jonathan (2016 թ․ մարտ). «Frequency and Complexity of De Novo Structural Mutation in Autism». The American Journal of Human Genetics. 98 (4): 667–679. doi:10.1016/j.ajhg.2016.02.018. PMC 4833290. PMID 27018473.
  • Iossifov, Ivan; Ronemus, Michael; Levy, Dan; Wang, Zihua; Hakker, Inessa; Rosenbaum, Julie; Yamrom, Boris; Lee, Yoon-ha; Narzisi, Giuseppe; Leotta, Anthony; Kendall, Jude; Grabowska, Ewa; Ma, Beicong; Marks, Steven; Rodgers, Linda; Stepansky, Asya; Troge, Jennifer; Andrews, Peter; Bekritsky, Mitchell; Pradhan, Kith; Ghiban, Elena; Kramer, Melissa; Parla, Jennifer; Demeter, Ryan; Fulton, Lucinda L.; Fulton, Robert S.; Magrini, Vincent J.; Ye, Kenny; Darnell, Jennifer C.; Darnell, Robert B.; Mardis, Elaine R.; Wilson, Richard K.; Schatz, Michael C.; McCombie, W. Richard; Wigler, Michael (2012 թ․ ապրիլ). «De Novo Gene Disruptions in Children on the Autistic Spectrum». Neuron. 74 (2): 285–299. doi:10.1016/j.neuron.2012.04.009. PMC 3619976. PMID 22542183.
  • De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Ercument Cicek, A.; Kou, Yan; Liu, Li; Fromer, Menachem; Walker, Susan; Singh, Tarjinder; Klei, Lambertus; Kosmicki, Jack; Fu, Shih-Chen; Aleksic, Branko; Biscaldi, Monica; Bolton, Patrick F.; Brownfeld, Jessica M.; Cai, Jinlu; Campbell, Nicholas G.; Carracedo, Angel; Chahrour, Maria H.; Chiocchetti, Andreas G.; Coon, Hilary; Crawford, Emily L.; Crooks, Lucy; Curran, Sarah R.; Dawson, Geraldine; Duketis, Eftichia; Fernandez, Bridget A.; Gallagher, Louise; Geller, Evan; Guter, Stephen J.; Sean Hill, R.; Ionita-Laza, Iuliana; Jimenez Gonzalez, Patricia; Kilpinen, Helena; Klauck, Sabine M.; Kolevzon, Alexander; Lee, Irene; Lei, Jing; Lehtimäki, Terho; Lin, Chiao-Feng; Ma’ayan, Avi; Marshall, Christian R.; McInnes, Alison L.; Neale, Benjamin; Owen, Michael J.; Ozaki, Norio; Parellada, Mara; Parr, Jeremy R.; Purcell, Shaun; Puura, Kaija; Rajagopalan, Deepthi; Rehnström, Karola; Reichenberg, Abraham; Sabo, Aniko; Sachse, Michael; Sanders, Stephan J.; Schafer, Chad; Schulte-Rüther, Martin; Skuse, David; Stevens, Christine; Szatmari, Peter; Tammimies, Kristiina; Valladares, Otto; Voran, Annette; Wang, Li-San; Weiss, Lauren A.; Jeremy Willsey, A.; Yu, Timothy W.; Yuen, Ryan K. C.; Cook, Edwin H.; Freitag, Christine M.; Gill, Michael; Hultman, Christina M.; Lehner, Thomas; Palotie, Aarno; Schellenberg, Gerard D.; Sklar, Pamela; State, Matthew W.; Sutcliffe, James S.; Walsh, Christopher A.; Scherer, Stephen W.; Zwick, Michael E.; Barrett, Jeffrey C.; Cutler, David J.; Roeder, Kathryn; Devlin, Bernie; Daly, Mark J.; Buxbaum, Joseph D. (2014 թ․ հոկտեմբերի 29). «Synaptic, transcriptional and chromatin genes disrupted in autism». Nature. 515 (7526): 209–215. doi:10.1038/nature13772. PMC 4402723. PMID 25363760.
  • Iossifov, Ivan; O’Roak, Brian J.; Sanders, Stephan J.; Ronemus, Michael; Krumm, Niklas; Levy, Dan; Stessman, Holly A.; Witherspoon, Kali T.; Vives, Laura; Patterson, Karynne E.; Smith, Joshua D.; Paeper, Bryan; Nickerson, Deborah A.; Dea, Jeanselle; Dong, Shan; Gonzalez, Luis E.; Mandell, Jeffrey D.; Mane, Shrikant M.; Murtha, Michael T.; Sullivan, Catherine A.; Walker, Michael F.; Waqar, Zainulabedin; Wei, Liping; Willsey, A. Jeremy; Yamrom, Boris; Lee, Yoon-ha; Grabowska, Ewa; Dalkic, Ertugrul; Wang, Zihua; Marks, Steven; Andrews, Peter; Leotta, Anthony; Kendall, Jude; Hakker, Inessa; Rosenbaum, Julie; Ma, Beicong; Rodgers, Linda; Troge, Jennifer; Narzisi, Giuseppe; Yoon, Seungtai; Schatz, Michael C.; Ye, Kenny; McCombie, W. Richard; Shendure, Jay; Eichler, Evan E.; State, Matthew W.; Wigler, Michael (2014 թ․ հոկտեմբերի 29). «The contribution of de novo coding mutations to autism spectrum disorder». Nature. 515 (7526): 216–221. doi:10.1038/nature13908. PMC 4313871. PMID 25363768.
  • Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma’ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San; Makarov, Vladimir; Polak, Paz; Yoon, Seungtai; Maguire, Jared; Crawford, Emily L.; Campbell, Nicholas G.; Geller, Evan T.; Valladares, Otto; Schafer, Chad; Liu, Han; Zhao, Tuo; Cai, Guiqing; Lihm, Jayon; Dannenfelser, Ruth; Jabado, Omar; Peralta, Zuleyma; Nagaswamy, Uma; Muzny, Donna; Reid, Jeffrey G.; Newsham, Irene; Wu, Yuanqing; Lewis, Lora; Han, Yi; Voight, Benjamin F.; Lim, Elaine; Rossin, Elizabeth; Kirby, Andrew; Flannick, Jason; Fromer, Menachem; Shakir, Khalid; Fennell, Tim; Garimella, Kiran; Banks, Eric; Poplin, Ryan; Gabriel, Stacey; DePristo, Mark; Wimbish, Jack R.; Boone, Braden E.; Levy, Shawn E.; Betancur, Catalina; Sunyaev, Shamil; Boerwinkle, Eric; Buxbaum, Joseph D.; Cook Jr, Edwin H.; Devlin, Bernie; Gibbs, Richard A.; Roeder, Kathryn; Schellenberg, Gerard D.; Sutcliffe, James S.; Daly, Mark J. (2012 թ․ ապրիլի 4). «Patterns and rates of exonic de novo mutations in autism spectrum disorders». Nature. 485 (7397): 242–245. doi:10.1038/nature11011. PMC 3613847. PMID 22495311.
  • Sanders, Stephan J.; Murtha, Michael T.; Gupta, Abha R.; Murdoch, John D.; Raubeson, Melanie J.; Willsey, A. Jeremy; Ercan-Sencicek, A. Gulhan; DiLullo, Nicholas M.; Parikshak, Neelroop N.; Stein, Jason L.; Walker, Michael F.; Ober, Gordon T.; Teran, Nicole A.; Song, Youeun; El-Fishawy, Paul; Murtha, Ryan C.; Choi, Murim; Overton, John D.; Bjornson, Robert D.; Carriero, Nicholas J.; Meyer, Kyle A.; Bilguvar, Kaya; Mane, Shrikant M.; Šestan, Nenad; Lifton, Richard P.; Günel, Murat; Roeder, Kathryn; Geschwind, Daniel H.; Devlin, Bernie; State, Matthew W. (2012 թ․ ապրիլի 4). «De novo mutations revealed by whole-exome sequencing are strongly associated with autism». Nature. 485 (7397): 237–241. doi:10.1038/nature10945. PMC 3667984. PMID 22495306.
  • O’Roak, Brian J.; Vives, Laura; Girirajan, Santhosh; Karakoc, Emre; Krumm, Niklas; Coe, Bradley P.; Levy, Roie; Ko, Arthur; Lee, Choli; Smith, Joshua D.; Turner, Emily H.; Stanaway, Ian B.; Vernot, Benjamin; Malig, Maika; Baker, Carl; Reilly, Beau; Akey, Joshua M.; Borenstein, Elhanan; Rieder, Mark J.; Nickerson, Deborah A.; Bernier, Raphael; Shendure, Jay; Eichler, Evan E. (2012 թ․ ապրիլի 4). «Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations». Nature. 485 (7397): 246–250. doi:10.1038/nature10989. PMC 3350576. PMID 22495309.
  • Ronemus, Michael; Iossifov, Ivan; Levy, Dan; Wigler, Michael (2014 թ․ հունվարի 16). «The role of de novo mutations in the genetics of autism spectrum disorders». Nature Reviews Genetics. 15 (2): 133–141. doi:10.1038/nrg3585. PMID 24430941.
  • Betancur, Catalina (2011 թ․ մարտ). «Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting». Brain Research. 1380: 42–77. doi:10.1016/j.brainres.2010.11.078. PMID 21129364.
  • Stefansson, Hreinn; Meyer-Lindenberg, Andreas; Steinberg, Stacy; Magnusdottir, Brynja; Morgen, Katrin; Arnarsdottir, Sunna; Bjornsdottir, Gyda; Walters, G. Bragi; Jonsdottir, Gudrun A.; Doyle, Orla M.; Tost, Heike; Grimm, Oliver; Kristjansdottir, Solveig; Snorrason, Heimir; Davidsdottir, Solveig R.; Gudmundsson, Larus J.; Jonsson, Gudbjorn F.; Stefansdottir, Berglind; Helgadottir, Isafold; Haraldsson, Magnus; Jonsdottir, Birna; Thygesen, Johan H.; Schwarz, Adam J.; Didriksen, Michael; Stensbøl, Tine B.; Brammer, Michael; Kapur, Shitij; Halldorsson, Jonas G.; Hreidarsson, Stefan; Saemundsen, Evald; Sigurdsson, Engilbert; Stefansson, Kari (2013 թ․ դեկտեմբերի 18). «CNVs conferring risk of autism or schizophrenia affect cognition in controls». Nature. 505 (7483): 361–366. doi:10.1038/nature12818. PMID 24352232.
  • Shinawi, M.; Liu, P.; Kang, S. H. L.; Shen, J.; Belmont, J. W.; Scott, D. A.; Probst, F. J.; Craigen, W. J.; Graham, B. H.; Pursley, A.; Clark, G.; Lee, J.; Proud, M.; Stocco, A.; Rodriguez, D. L.; Kozel, B. A.; Sparagana, S.; Roeder, E. R.; McGrew, S. G.; Kurczynski, T. W.; Allison, L. J.; Amato, S.; Savage, S.; Patel, A.; Stankiewicz, P.; Beaudet, A. L.; Cheung, S. W.; Lupski, J. R. (2009 թ․ նոյեմբերի 12). «Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size». Journal of Medical Genetics. 47 (5): 332–341. doi:10.1136/jmg.2009.073015. PMC 3158566. PMID 19914906.
  • Brandler, William M.; Sebat, Jonathan (2015 թ․ հունվարի 14). «From De Novo Mutations to Personalized Therapeutic Interventions in Autism». Annual Review of Medicine. 66 (1): 487–507. doi:10.1146/annurev-med-091113-024550. PMID 25587659.
  • «Pathophysiology of autism spectrum disorders: revisiting gastrointestinal involvement and immune imbalance». World J Gastroenterol (Review). 20 (29): 9942–51. 2014. doi:10.3748/wjg.v20.i29.9942. PMC 4123375. PMID 25110424.{{cite journal}}: CS1 սպաս․ չպիտակված ազատ DOI (link)
  • «Neurodevelopment: The Impact of Nutrition and Inflammation During Preconception and Pregnancy in Low-Resource Settings». Pediatrics (Review). 139 (Suppl 1): S38–S49. 2017. doi:10.1542/peds.2016-2828F. PMID 28562247.

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