Cited In for PMID: 19502243

Year	Number of Results
2009	1
2011	2
2012	1
2013	3
2014	2
2015	1
2016	2
2017	3
2018	1
2019	1
2021	1
2023	2
2024	0

1

17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction.

Grisart B, Willatt L, Destrée A, Fryns JP, Rack K, de Ravel T, Rosenfeld J, Vermeesch JR, Verellen-Dumoulin C, Sandford R. Grisart B, et al. J Med Genet. 2009 Aug;46(8):524-30. doi: 10.1136/jmg.2008.065367. Epub 2009 Jun 4. J Med Genet. 2009. PMID: 19502243

2

De novo network analysis reveals autism causal genes and developmental links to co-occurring traits.

Miller CJ, Golovina E, Wicker JS, Jacobsen JC, O'Sullivan JM. Miller CJ, et al. Life Sci Alliance. 2023 Aug 8;6(10):e202302142. doi: 10.26508/lsa.202302142. Print 2023 Oct. Life Sci Alliance. 2023. PMID: 37553252 Free PMC article.

3

PARK2 Microdeletion or Duplications Have Been Implicated in Different Neurological Disorders Including Early Onset Parkinson Disease.

Ahmad A, Nkosi D, Iqbal MA. Ahmad A, et al. Genes (Basel). 2023 Feb 27;14(3):600. doi: 10.3390/genes14030600. Genes (Basel). 2023. PMID: 36980871 Free PMC article.

4

Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders.

Mosley TJ, Johnston HR, Cutler DJ, Zwick ME, Mulle JG. Mosley TJ, et al. BMC Med Genomics. 2021 Jun 9;14(1):154. doi: 10.1186/s12920-021-00999-8. BMC Med Genomics. 2021. PMID: 34107974 Free PMC article.

5

Impact of polymorphic transposable elements on transcription in lymphoblastoid cell lines from public data.

Spirito G, Mangoni D, Sanges R, Gustincich S. Spirito G, et al. BMC Bioinformatics. 2019 Nov 22;20(Suppl 9):495. doi: 10.1186/s12859-019-3113-x. BMC Bioinformatics. 2019. PMID: 31757210 Free PMC article.

6

Analyses of karyotype by G-banding and high-resolution microarrays in a gender dysphoria population.

Fernández R, Guillamón A, Gómez-Gil E, Esteva I, Almaraz MC, Cortés-Cortés J, Lamas B, Lema E, Pásaro E. Fernández R, et al. Genes Genomics. 2018 May;40(5):465-473. doi: 10.1007/s13258-017-0646-0. Epub 2018 Jan 22. Genes Genomics. 2018. PMID: 29892954

7

Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition.

Arbogast T, Iacono G, Chevalier C, Afinowi NO, Houbaert X, van Eede MC, Laliberte C, Birling MC, Linda K, Meziane H, Selloum M, Sorg T, Nadif Kasri N, Koolen DA, Stunnenberg HG, Henkelman RM, Kopanitsa M, Humeau Y, De Vries BBA, Herault Y. Arbogast T, et al. PLoS Genet. 2017 Jul 13;13(7):e1006886. doi: 10.1371/journal.pgen.1006886. eCollection 2017 Jul. PLoS Genet. 2017. PMID: 28704368 Free PMC article.

8

Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital Anomalies.

Rosenfeld JA, Patel A. Rosenfeld JA, et al. J Pediatr Genet. 2017 Mar;6(1):42-50. doi: 10.1055/s-0036-1584306. Epub 2016 May 30. J Pediatr Genet. 2017. PMID: 28180026 Free PMC article. Review.

9

17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.

Le Guennec K, Quenez O, Nicolas G, Wallon D, Rousseau S, Richard AC, Alexander J, Paschou P, Charbonnier C, Bellenguez C, Grenier-Boley B, Lechner D, Bihoreau MT, Olaso R, Boland A, Meyer V, Deleuze JF, Amouyel P, Munter HM, Bourque G, Lathrop M, Frebourg T, Redon R, Letenneur L, Dartigues JF, Martinaud O, Kalev O, Mehrabian S, Traykov L, Ströbel T, Le Ber I, Caroppo P, Epelbaum S, Jonveaux T, Pasquier F, Rollin-Sillaire A, Génin E, Guyant-Maréchal L, Kovacs GG, Lambert JC, Hannequin D, Campion D, Rovelet-Lecrux A. Le Guennec K, et al. Mol Psychiatry. 2017 Aug;22(8):1119-1125. doi: 10.1038/mp.2016.226. Epub 2016 Dec 13. Mol Psychiatry. 2017. PMID: 27956742

10

Functional consequences of 17q21.31/WNT3-WNT9B amplification in hPSCs with respect to neural differentiation.

Lee CT, Bendriem RM, Kindberg AA, Worden LT, Williams MP, Drgon T, Mallon BS, Harvey BK, Richie CT, Hamilton RS, Chen J, Errico SL, Tsai SY, Uhl GR, Freed WJ. Lee CT, et al. Cell Rep. 2015 Feb 3;10(4):616-32. doi: 10.1016/j.celrep.2014.12.050. Epub 2015 Jan 29. Cell Rep. 2015. PMID: 25640183 Free PMC article.

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