References analysis of the Wikipedia article "ASH1L" in the Spanish version

adsabs.harvard.edu (Global: 14^th place; Spanish: 43^rd place)

Tanaka Y, Kawahashi K, Katagiri Z, Nakayama Y, Mahajan M, Kioussis D (2011). «Dual function of histone H3 lysine 36 methyltransferase ASH1 in regulation of Hox gene expression». PLOS ONE 6 (11): e28171. Bibcode:2011PLoSO...628171T. PMC 3225378. PMID 22140534. doi:10.1371/journal.pone.0028171.

Nakamura T, Blechman J, Tada S, Rozovskaia T, Itoyama T, Bullrich F, Mazo A, Croce CM, Geiger B, Canaani E (June 2000). «huASH1 protein, a putative transcription factor encoded by a human homologue of the Drosophila ash1 gene, localizes to both nuclei and cell-cell tight junctions». Proceedings of the National Academy of Sciences of the United States of America 97 (13): 7284-7289. Bibcode:2000PNAS...97.7284N. PMC 16537. PMID 10860993. doi:10.1073/pnas.97.13.7284.

Tasic B, Yao Z, Graybuck LT, Smith KA, Nguyen TN, Bertagnolli D, Goldy J, Garren E, Economo MN, Viswanathan S, Penn O, Bakken T, Menon V, Miller J, Fong O, Hirokawa KE, Lathia K, Rimorin C, Tieu M, Larsen R, Casper T, Barkan E, Kroll M, Parry S, Shapovalova NV, Hirschstein D, Pendergraft J, Sullivan HA, Kim TK, Szafer A, Dee N, Groblewski P, Wickersham I, Cetin A, Harris JA, Levi BP, Sunkin SM, Madisen L, Daigle TL, Looger L, Bernard A, Phillips J, Lein E, Hawrylycz M, Svoboda K, Jones AR, Koch C, Zeng H (November 2018). «Shared and distinct transcriptomic cell types across neocortical areas». Nature 563 (7729): 72-78. Bibcode:2018Natur.563...72T. PMC 6456269. PMID 30382198. doi:10.1038/s41586-018-0654-5.

Miller JA, Ding SL, Sunkin SM, Smith KA, Ng L, Szafer A, Ebbert A, Riley ZL, Royall JJ, Aiona K, Arnold JM, Bennet C, Bertagnolli D, Brouner K, Butler S, Caldejon S, Carey A, Cuhaciyan C, Dalley RA, Dee N, Dolbeare TA, Facer BA, Feng D, Fliss TP, Gee G, Goldy J, Gourley L, Gregor BW, Gu G, Howard RE, Jochim JM, Kuan CL, Lau C, Lee CK, Lee F, Lemon TA, Lesnar P, McMurray B, Mastan N, Mosqueda N, Naluai-Cecchini T, Ngo NK, Nyhus J, Oldre A, Olson E, Parente J, Parker PD, Parry SE, Stevens A, Pletikos M, Reding M, Roll K, Sandman D, Sarreal M, Shapouri S, Shapovalova NV, Shen EH, Sjoquist N, Slaughterbeck CR, Smith M, Sodt AJ, Williams D, Zöllei L, Fischl B, Gerstein MB, Geschwind DH, Glass IA, Hawrylycz MJ, Hevner RF, Huang H, Jones AR, Knowles JA, Levitt P, Phillips JW, Sestan N, Wohnoutka P, Dang C, Bernard A, Hohmann JG, Lein ES (April 2014). «Transcriptional landscape of the prenatal human brain». Nature 508 (7495): 199-206. Bibcode:2014Natur.508..199M. PMC 4105188. PMID 24695229. doi:10.1038/nature13185.

Zhu T, Liang C, Li D, Tian M, Liu S, Gao G, Guan JS (May 2016). «Histone methyltransferase Ash1L mediates activity-dependent repression of neurexin-1α». Scientific Reports 6: 26597. Bibcode:2016NatSR...626597Z. PMC 4882582. PMID 27229316. doi:10.1038/srep26597.

Lein ES, Hawrylycz MJ, Ao N, Ayres M, Bensinger A, Bernard A, Boe AF, Boguski MS, Brockway KS, Byrnes EJ, Chen L, Chen L, Chen TM, Chin MC, Chong J, Crook BE, Czaplinska A, Dang CN, Datta S, Dee NR, Desaki AL, Desta T, Diep E, Dolbeare TA, Donelan MJ, Dong HW, Dougherty JG, Duncan BJ, Ebbert AJ, Eichele G, Estin LK, Faber C, Facer BA, Fields R, Fischer SR, Fliss TP, Frensley C, Gates SN, Glattfelder KJ, Halverson KR, Hart MR, Hohmann JG, Howell MP, Jeung DP, Johnson RA, Karr PT, Kawal R, Kidney JM, Knapik RH, Kuan CL, Lake JH, Laramee AR, Larsen KD, Lau C, Lemon TA, Liang AJ, Liu Y, Luong LT, Michaels J, Morgan JJ, Morgan RJ, Mortrud MT, Mosqueda NF, Ng LL, Ng R, Orta GJ, Overly CC, Pak TH, Parry SE, Pathak SD, Pearson OC, Puchalski RB, Riley ZL, Rockett HR, Rowland SA, Royall JJ, Ruiz MJ, Sarno NR, Schaffnit K, Shapovalova NV, Sivisay T, Slaughterbeck CR, Smith SC, Smith KA, Smith BI, Sodt AJ, Stewart NN, Stumpf KR, Sunkin SM, Sutram M, Tam A, Teemer CD, Thaller C, Thompson CL, Varnam LR, Visel A, Whitlock RM, Wohnoutka PE, Wolkey CK, Wong VY, Wood M, Yaylaoglu MB, Young RC, Youngstrom BL, Yuan XF, Zhang B, Zwingman TA, Jones AR (January 2007). «Genome-wide atlas of gene expression in the adult mouse brain». Nature 445 (7124): 168-176. Bibcode:2007Natur.445..168L. PMID 17151600. doi:10.1038/nature05453.

De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, Biscaldi M, Bolton PF, Brownfeld JM, Cai J, Campbell NG, Carracedo A, Chahrour MH, Chiocchetti AG, Coon H, Crawford EL, Curran SR, Dawson G, Duketis E, Fernandez BA, Gallagher L, Geller E, Guter SJ, Hill RS, Ionita-Laza J, Jimenz Gonzalez P, Kilpinen H, Klauck SM, Kolevzon A, Lee I, Lei I, Lei J, Lehtimäki T, Lin CF, Ma'ayan A, Marshall CR, McInnes AL, Neale B, Owen MJ, Ozaki N, Parellada M, Parr JR, Purcell S, Puura K, Rajagopalan D, Rehnström K, Reichenberg A, Sabo A, Sachse M, Sanders SJ, Schafer C, Schulte-Rüther M, Skuse D, Stevens C, Szatmari P, Tammimies K, Valladares O, Voran A, Li-San W, Weiss LA, Willsey AJ, Yu TW, Yuen RK, Cook EH, Freitag CM, Gill M, Hultman CM, Lehner T, Palotie A, Schellenberg GD, Sklar P, State MW, Sutcliffe JS, Walsh CA, Scherer SW, Zwick ME, Barett JC, Cutler DJ, Roeder K, Devlin B, Daly MJ, Buxbaum JD (November 2014). «Synaptic, transcriptional and chromatin genes disrupted in autism». Nature 515 (7526): 209-215. Bibcode:2014Natur.515..209.. PMC 4402723. PMID 25363760. doi:10.1038/nature13772.

Homsy J, Zaidi S, Shen Y, Ware JS, Samocha KE, Karczewski KJ, DePalma SR, McKean D, Wakimoto H, Gorham J, Jin SC, Deanfield J, Giardini A, Porter GA, Kim R, Bilguvar K, López-Giráldez F, Tikhonova I, Mane S, Romano-Adesman A, Qi H, Vardarajan B, Ma L, Daly M, Roberts AE, Russell MW, Mital S, Newburger JW, Gaynor JW, Breitbart RE, Iossifov I, Ronemus M, Sanders SJ, Kaltman JR, Seidman JG, Brueckner M, Gelb BD, Goldmuntz E, Lifton RP, Seidman CE, Chung WK (December 2015). «De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies». Science 350 (6265): 1262-1266. Bibcode:2015Sci...350.1262H. PMC 4890146. PMID 26785492. doi:10.1126/science.aac9396.

Wang T, Guo H, Xiong B, Stessman HA, Wu H, Coe BP, Turner TN, Liu Y, Zhao W, Hoekzema K, Vives L, Xia L, Tang M, Ou J, Chen B, Shen Y, Xun G, Long M, Lin J, Kronenberg ZN, Peng Y, Bai T, Li H, Ke X, Hu Z, Zhao J, Zou X, Xia K, Eichler EE (November 2016). «De novo genic mutations among a Chinese autism spectrum disorder cohort». Nature Communications 7: 13316. Bibcode:2016NatCo...713316W. PMC 5105161. PMID 27824329. doi:10.1038/ncomms13316.

Wang T, Hoekzema K, Vecchio D, Wu H, Sulovari A, Coe BP, Gillentine MA, Wilfert AB, Perez-Jurado LA, Kvarnung M, Sleyp Y, Earl RK, Rosenfeld JA, Geisheker MR, Han L, Du B, Barnett C, Thompson E, Shaw M, Carroll R, Friend K, Catford R, Palmer EE, Zou X, Ou J, Li H, Guo H, Gerdts J, Avola E, Calabrese G, Elia M, Greco D, Lindstrand A, Nordgren A, Anderlid BM, Vandeweyer G, Van Dijck A, Van der Aa N, McKenna B, Hancarova M, Bendova S, Havlovicova M, Malerba G, Bernardina BD, Muglia P, van Haeringen A, Hoffer MJ, Franke B, Cappuccio G, Delatycki M, Lockhart PJ, Manning MA, Liu P, Scheffer IE, Brunetti-Pierri N, Rommelse N, Amaral DG, Santen GW, Trabetti E, Sedláček Z, Michaelson JJ, Pierce K, Courchesne E, Kooy RF, Nordenskjöld M, Romano C, Peeters H, Bernier RA, Gecz J, Xia K, Eichler EE (October 2020). «Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders». Nature Communications 11 (1): 4932. Bibcode:2020NatCo..11.4932W. PMC 7530681. PMID 33004838. doi:10.1038/s41467-020-18723-y.

Iossifov I, O'Roak BJ, Sanders SJ, Ronemus M, Krumm N, Levy D, Stessman HA, Witherspoon KT, Vives L, Patterson KE, Smith JD, Paeper B, Nickerson DA, Dea J, Dong S, Gonzalez LE, Mandell JD, Mane SM, Murtha MT, Sullivan CA, Walker MF, Waqar Z, Wei L, Willsey AJ, Yamrom B, Lee YH, Grabowska E, Dalkic E, Wang Z, Marks S, Andrews P, Leotta A, Kendall J, Hakker I, Rosenbaum J, Ma B, Rodgers L, Troge J, Narzisi G, Yoon S, Schatz MC, Ye K, McCombie WR, Shendure J, Eichler EE, State MW, Wigler M (November 2014). «The contribution of de novo coding mutations to autism spectrum disorder». Nature 515 (7526): 216-221. Bibcode:2014Natur.515..216I. PMC 4313871. PMID 25363768. doi:10.1038/nature13908.

archive.org (Global: 6^th place; Spanish: 4^th place)

Rozovskaia T, Tillib S, Smith S, Sedkov Y, Rozenblatt-Rosen O, Petruk S, Yano T, Nakamura T, Ben-Simchon L, Gildea J, Croce CM, Shearn A, Canaani E, Mazo A (September 1999). «Trithorax and ASH1 interact directly and associate with the trithorax group-responsive bxd region of the Ultrabithorax promoter». Molecular and Cellular Biology 19 (9): 6441-6447. PMC 84613. PMID 10454589. doi:10.1128/MCB.19.9.6441.

An S, Yeo KJ, Jeon YH, Song JJ (March 2011). «Crystal structure of the human histone methyltransferase ASH1L catalytic domain and its implications for the regulatory mechanism». The Journal of Biological Chemistry 286 (10): 8369-8374. PMC 3048721. PMID 21239497. doi:10.1074/jbc.M110.203380.

Gregory GD, Vakoc CR, Rozovskaia T, Zheng X, Patel S, Nakamura T, Canaani E, Blobel GA (December 2007). «Mammalian ASH1L is a histone methyltransferase that occupies the transcribed region of active genes». Molecular and Cellular Biology 27 (24): 8466-8479. PMC 2169421. PMID 17923682. doi:10.1128/MCB.00993-07.

Tammimies K, Marshall CR, Walker S, Kaur G, Thiruvahindrapuram B, Lionel AC, Yuen RK, Uddin M, Roberts W, Weksberg R, Woodbury-Smith M, Zwaigenbaum L, Anagnostou E, Wang Z, Wei J, Howe JL, Gazzellone MJ, Lau L, Sung WW, Whitten K, Vardy C, Crosbie V, Tsang B, D'Abate L, Tong WW, Luscombe S, Doyle T, Carter MT, Szatmari P, Stuckless S, Merico D, Stavropoulos DJ, Scherer SW, Fernandez BA (September 2015). «Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder». JAMA 314 (9): 895-903. PMID 26325558. doi:10.1001/jama.2015.10078.

de Ligt J, Willemsen MH, van Bon BW, Kleefstra T, Yntema HG, Kroes T, Vulto-van Silfhout AT, Koolen DA, de Vries P, Gilissen C, del Rosario M, Hoischen A, Scheffer H, de Vries BB, Brunner HG, Veltman JA, Vissers LE (November 2012). «Diagnostic exome sequencing in persons with severe intellectual disability». The New England Journal of Medicine 367 (20): 1921-1929. PMID 23033978. doi:10.1056/NEJMoa1206524.

doi.org (Global: 2^nd place; Spanish: 2^nd place)

dx.doi.org

Uhlén M, Fagerberg L, Hallström BM, Lindskog C, Oksvold P, Mardinoglu A, Sivertsson Å, Kampf C, Sjöstedt E, Asplund A, Olsson I, Edlund K, Lundberg E, Navani S, Szigyarto CA, Odeberg J, Djureinovic D, Takanen JO, Hober S, Alm T, Edqvist PH, Berling H, Tegel H, Mulder J, Rockberg J, Nilsson P, Schwenk JM, Hamsten M, von Feilitzen K, Forsberg M, Persson L, Johansson F, Zwahlen M, von Heijne G, Nielsen J, Pontén F (January 2015). «Proteomics. Tissue-based map of the human proteome». Science 347 (6220): 1260419. PMID 25613900. doi:10.1126/science.1260419.

Smith CM, Hayamizu TF, Finger JH, Bello SM, McCright IJ, Xu J, Baldarelli RM, Beal JS, Campbell J, Corbani LE, Frost PJ, Lewis JR, Giannatto SC, Miers D, Shaw DR, Kadin JA, Richardson JE, Smith CL, Ringwald M (January 2019). «The mouse Gene Expression Database (GXD): 2019 update». Nucleic Acids Research 47 (D1): D774-D779. PMC 6324054. PMID 30335138. doi:10.1093/nar/gky922.

Fagerberg L, Hallström BM, Oksvold P, Kampf C, Djureinovic D, Odeberg J, Habuka M, Tahmasebpoor S, Danielsson A, Edlund K, Asplund A, Sjöstedt E, Lundberg E, Szigyarto CA, Skogs M, Takanen JO, Berling H, Tegel H, Mulder J, Nilsson P, Schwenk JM, Lindskog C, Danielsson F, Mardinoglu A, Sivertsson A, von Feilitzen K, Forsberg M, Zwahlen M, Olsson I, Navani S, Huss M, Nielsen J, Ponten F, Uhlén M (February 2014). «Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics». Molecular & Cellular Proteomics 13 (2): 397-406. PMC 3916642. PMID 24309898. doi:10.1074/mcp.m113.035600.

Zhang Y, Sloan SA, Clarke LE, Caneda C, Plaza CA, Blumenthal PD, Vogel H, Steinberg GK, Edwards MS, Li G, Duncan JA, Cheshier SH, Shuer LM, Chang EF, Grant GA, Gephart MG, Barres BA (January 2016). «Purification and Characterization of Progenitor and Mature Human Astrocytes Reveals Transcriptional and Functional Differences with Mouse». Neuron 89 (1): 37-53. PMC 4707064. PMID 26687838. doi:10.1016/j.neuron.2015.11.013.

Zhang Y, Chen K, Sloan SA, Bennett ML, Scholze AR, O'Keeffe S, Phatnani HP, Guarnieri P, Caneda C, Ruderisch N, Deng S, Liddelow SA, Zhang C, Daneman R, Maniatis T, Barres BA, Wu JQ (September 2014). «An RNA-sequencing transcriptome and splicing database of glia, neurons, and vascular cells of the cerebral cortex». The Journal of Neuroscience 34 (36): 11929-11947. PMC 4152602. PMID 25186741. doi:10.1523/JNEUROSCI.1860-14.2014.

Cheon S, Culver AM, Bagnell AM, Ritchie FD, Vacharasin JM, McCord MM, Papendorp CM, Chukwurah E, Smith AJ, Cowen MH, Moreland TA, Ghate PS, Davis SW, Liu JS, Lizarraga SB (April 2022). «Counteracting epigenetic mechanisms regulate the structural development of neuronal circuitry in human neurons». Molecular Psychiatry 27 (4): 2291-2303. PMC 9133078. PMID 35210569. doi:10.1038/s41380-022-01474-1.

Elsen GE, Bedogni F, Hodge RD, Bammler TK, MacDonald JW, Lindtner S, Rubenstein JL, Hevner RF (2018). «The Epigenetic Factor Landscape of Developing Neocortex Is Regulated by Transcription Factors Pax6→ Tbr2→ Tbr1». Frontiers in Neuroscience 12: 571. PMC 6113890. PMID 30186101. doi:10.3389/fnins.2018.00571.

Tanaka Y, Katagiri Z, Kawahashi K, Kioussis D, Kitajima S (August 2007). «Trithorax-group protein ASH1 methylates histone H3 lysine 36». Gene 397 (1–2): 161-168. PMID 17544230. doi:10.1016/j.gene.2007.04.027.

Faundes V, Newman WG, Bernardini L, Canham N, Clayton-Smith J, Dallapiccola B, Davies SJ, Demos MK, Goldman A, Gill H, Horton R, Kerr B, Kumar D, Lehman A, McKee S, Morton J, Parker MJ, Rankin J, Robertson L, Temple IK, Banka S (January 2018). «Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders». American Journal of Human Genetics 102 (1): 175-187. PMC 5778085. PMID 29276005. doi:10.1016/j.ajhg.2017.11.013.

Grozeva D, Carss K, Spasic-Boskovic O, Tejada MI, Gecz J, Shaw M, Corbett M, Haan E, Thompson E, Friend K, Hussain Z, Hackett A, Field M, Renieri A, Stevenson R, Schwartz C, Floyd JA, Bentham J, Cosgrove C, Keavney B, Bhattacharya S, Hurles M, Raymond FL (December 2015). «Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability». Human Mutation 36 (12): 1197-1204. PMC 4833192. PMID 26350204. doi:10.1002/humu.22901.

Okamoto N, Miya F, Tsunoda T, Kato M, Saitoh S, Yamasaki M, Kanemura Y, Kosaki K (June 2017). «Novel MCA/ID syndrome with ASH1L mutation». American Journal of Medical Genetics. Part A 173 (6): 1644-1648. PMID 28394464. doi:10.1002/ajmg.a.38193.

Shen W, Krautscheid P, Rutz AM, Bayrak-Toydemir P, Dugan SL (January 2019). «De novo loss-of-function variants of ASH1L are associated with an emergent neurodevelopmental disorder». European Journal of Medical Genetics 62 (1): 55-60. PMID 29753921. doi:10.1016/j.ejmg.2018.05.003.

Liu H, Liu DT, Lan S, Yang Y, Huang J, Huang J, Fang L (September 2021). «ASH1L mutation caused seizures and intellectual disability in twin sisters». Journal of Clinical Neuroscience 91: 69-74. PMID 34373061. doi:10.1016/j.jocn.2021.06.038.

Tang S, Addis L, Smith A, Topp SD, Pendziwiat M, Mei D, Parker A, Agrawal S, Hughes E, Lascelles K, Williams RE, Fallon P, Robinson R, Cross HJ, Hedderly T, Eltze C, Kerr T, Desurkar A, Hussain N, Kinali M, Bagnasco I, Vassallo G, Whitehouse W, Goyal S, Absoud M, Møller RS, Helbig I, Weber YG, Marini C, Guerrini R, Simpson MA, Pal DK (May 2020). «Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures». Epilepsia 61 (5): 995-1007. PMID 32469098. doi:10.1111/epi.16508.

Stessman HA, Xiong B, Coe BP, Wang T, Hoekzema K, Fenckova M, Kvarnung M, Gerdts J, Trinh S, Cosemans N, Vives L, Lin J, Turner TN, Santen G, Ruivenkamp C, Kriek M, van Haeringen A, Aten E, Friend K, Liebelt J, Barnett C, Haan E, Shaw M, Gecz J, Anderlid BM, Nordgren A, Lindstrand A, Schwartz C, Kooy RF, Vandeweyer G, Helsmoortel C, Romano C, Alberti A, Vinci M, Avola E, Giusto S, Courchesne E, Pramparo T, Pierce K, Nalabolu S, Amaral DG, Scheffer IE, Delatycki MB, Lockhart PJ, Hormozdiari F, Harich B, Castells-Nobau A, Xia K, Peeters H, Nordenskjöld M, Schenck A, Bernier RA, Eichler EE (April 2017). «Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases». Nature Genetics 49 (4): 515-526. PMC 5374041. PMID 28191889. doi:10.1038/ng.3792.

Ruzzo EK, Pérez-Cano L, Jung JY, Wang LK, Kashef-Haghighi D, Hartl C, Singh C, Xu J, Hoekstra JN, Leventhal O, Leppä VM, Gandal MJ, Paskov K, Stockham N, Polioudakis D, Lowe JK, Prober DA, Geschwind DH, Wall DP (August 2019). «Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks». Cell 178 (4): 850-866.e26. PMC 7102900. PMID 31398340. doi:10.1016/j.cell.2019.07.015.

Willsey AJ, Sanders SJ, Li M, Dong S, Tebbenkamp AT, Muhle RA, Reilly SK, Lin L, Fertuzinhos S, Miller JA, Murtha MT, Bichsel C, Niu W, Cotney J, Ercan-Sencicek AG, Gockley J, Gupta AR, Han W, He X, Hoffman EJ, Klei L, Lei J, Liu W, Liu L, Lu C, Xu X, Zhu Y, Mane SM, Lein ES, Wei L, Noonan JP, Roeder K, Devlin B, Sestan N, State MW (November 2013). «Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism». Cell 155 (5): 997-1007. PMC 3995413. PMID 24267886. doi:10.1016/j.cell.2013.10.020.

Guo H, Wang T, Wu H, Long M, Coe BP, Li H, Xun G, Ou J, Chen B, Duan G, Bai T, Zhao N, Shen Y, Li Y, Wang Y, Zhang Y, Baker C, Liu Y, Pang N, Huang L, Han L, Jia X, Liu C, Ni H, Yang X, Xia L, Chen J, Shen L, Li Y, Zhao R, Zhao W, Peng J, Pan Q, Long Z, Su W, Tan J, Du X, Ke X, Yao M, Hu Z, Zou X, Zhao J, Bernier RA, Eichler EE, Xia K (2018). «Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model». Molecular Autism 9: 64. PMC 6293633. PMID 30564305. doi:10.1186/s13229-018-0247-z.

Zhou X, Feliciano P, Shu C, Wang T, Astrovskaya I, Hall JB, Obiajulu JU, Wright JR, Murali SC, Xu SX, Brueggeman L, Thomas TR, Marchenko O, Fleisch C, Barns SD, Snyder LG, Han B, Chang TS, Turner TN, Harvey WT, Nishida A, O'Roak BJ, Geschwind DH, Michaelson JJ, Volfovsky N, Eichler EE, Shen Y, Chung WK (September 2022). «Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes». Nature Genetics 54 (9): 1305-1319. PMC 9470534. PMID 35982159. doi:10.1038/s41588-022-01148-2.

C Yuen RK, Merico D, Bookman M, L Howe J, Thiruvahindrapuram B, Patel RV, Whitney J, Deflaux N, Bingham J, Wang Z, Pellecchia G, Buchanan JA, Walker S, Marshall CR, Uddin M, Zarrei M, Deneault E, D'Abate L, Chan AJ, Koyanagi S, Paton T, Pereira SL, Hoang N, Engchuan W, Higginbotham EJ, Ho K, Lamoureux S, Li W, MacDonald JR, Nalpathamkalam T, Sung WW, Tsoi FJ, Wei J, Xu L, Tasse AM, Kirby E, Van Etten W, Twigger S, Roberts W, Drmic I, Jilderda S, Modi BM, Kellam B, Szego M, Cytrynbaum C, Weksberg R, Zwaigenbaum L, Woodbury-Smith M, Brian J, Senman L, Iaboni A, Doyle-Thomas K, Thompson A, Chrysler C, Leef J, Savion-Lemieux T, Smith IM, Liu X, Nicolson R, Seifer V, Fedele A, Cook EH, Dager S, Estes A, Gallagher L, Malow BA, Parr JR, Spence SJ, Vorstman J, Frey BJ, Robinson JT, Strug LJ, Fernandez BA, Elsabbagh M, Carter MT, Hallmayer J, Knoppers BM, Anagnostou E, Szatmari P, Ring RH, Glazer D, Pletcher MT, Scherer SW (April 2017). «Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder». Nature Neuroscience 20 (4): 602-611. PMC 5501701. PMID 28263302. doi:10.1038/nn.4524.

Krumm N, Turner TN, Baker C, Vives L, Mohajeri K, Witherspoon K, Raja A, Coe BP, Stessman HA, He ZX, Leal SM, Bernier R, Eichler EE (June 2015). «Excess of rare, inherited truncating mutations in autism». Nature Genetics 47 (6): 582-588. PMC 4449286. PMID 25961944. doi:10.1038/ng.3303.

Mitani T, Isikay S, Gezdirici A, Gulec EY, Punetha J, Fatih JM, Herman I, Akay G, Du H, Calame DG, Ayaz A, Tos T, Yesil G, Aydin H, Geckinli B, Elcioglu N, Candan S, Sezer O, Erdem HB, Gul D, Demiral E, Elmas M, Yesilbas O, Kilic B, Gungor S, Ceylan AC, Bozdogan S, Ozalp O, Cicek S, Aslan H, Yalcintepe S, Topcu V, Bayram Y, Grochowski CM, Jolly A, Dawood M, Duan R, Jhangiani SN, Doddapaneni H, Hu J, Muzny DM, Marafi D, Akdemir ZC, Karaca E, Carvalho CM, Gibbs RA, Posey JE, Lupski JR, Pehlivan D (October 2021). «High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population». American Journal of Human Genetics 108 (10): 1981-2005. PMC 8546040. PMID 34582790. doi:10.1016/j.ajhg.2021.08.009.

Dhaliwal J, Qiao Y, Calli K, Martell S, Race S, Chijiwa C, Glodjo A, Jones S, Rajcan-Separovic E, Scherer SW, Lewis S (July 2021). «Contribution of Multiple Inherited Variants to Autism Spectrum Disorder (ASD) in a Family with 3 Affected Siblings». Genes 12 (7): 1053. PMC 8303619. PMID 34356069. doi:10.3390/genes12071053.

Aspromonte MC, Bellini M, Gasparini A, Carraro M, Bettella E, Polli R, Cesca F, Bigoni S, Boni S, Carlet O, Negrin S, Mammi I, Milani D, Peron A, Sartori S, Toldo I, Soli F, Turolla L, Stanzial F, Benedicenti F, Marino-Buslje C, Tosatto SC, Murgia A, Leonardi E (September 2019). «Characterization of intellectual disability and autism comorbidity through gene panel sequencing». Human Mutation 40 (9): 1346-1363. PMC 7428836. PMID 31209962. doi:10.1002/humu.23822.

nih.gov (Global: 5^th place; Spanish: 5^th place)

ncbi.nlm.nih.gov

«Human PubMed Reference:».

«Mouse PubMed Reference:».

ASH1L (Spanish Wikipedia)

adsabs.harvard.edu (Global: 14^th place; Spanish: 43^rd place)

archive.org (Global: 6^th place; Spanish: 4^th place)

clinicalgenome.org (Global: low place; Spanish: low place)

search.clinicalgenome.org

doi.org (Global: 2^nd place; Spanish: 2^nd place)

dx.doi.org

jensenlab.org (Global: low place; Spanish: low place)

diseases.jensenlab.org

malacards.org (Global: low place; Spanish: 7,884^th place)

nih.gov (Global: 5^th place; Spanish: 5^th place)

ncbi.nlm.nih.gov

proteinatlas.org (Global: low place; Spanish: low place)

sfari.org (Global: low place; Spanish: low place)

gene.sfari.org

uniprot.org (Global: 2,402^nd place; Spanish: 2,752^nd place)

wikidata.org (Global: 10^th place; Spanish: 253^rd place)

ASH1L (Spanish Wikipedia)

adsabs.harvard.edu (Global: 14th place; Spanish: 43rd place)

archive.org (Global: 6th place; Spanish: 4th place)

clinicalgenome.org (Global: low place; Spanish: low place)

search.clinicalgenome.org

doi.org (Global: 2nd place; Spanish: 2nd place)

dx.doi.org

jensenlab.org (Global: low place; Spanish: low place)

diseases.jensenlab.org

malacards.org (Global: low place; Spanish: 7,884th place)

nih.gov (Global: 5th place; Spanish: 5th place)

ncbi.nlm.nih.gov

proteinatlas.org (Global: low place; Spanish: low place)

sfari.org (Global: low place; Spanish: low place)

gene.sfari.org

uniprot.org (Global: 2,402nd place; Spanish: 2,752nd place)

wikidata.org (Global: 10th place; Spanish: 253rd place)

adsabs.harvard.edu (Global: 14^th place; Spanish: 43^rd place)

archive.org (Global: 6^th place; Spanish: 4^th place)

doi.org (Global: 2^nd place; Spanish: 2^nd place)

malacards.org (Global: low place; Spanish: 7,884^th place)

nih.gov (Global: 5^th place; Spanish: 5^th place)

uniprot.org (Global: 2,402^nd place; Spanish: 2,752^nd place)

wikidata.org (Global: 10^th place; Spanish: 253^rd place)