Similar articles for PMID: 23832105

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1

Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation.

Liao C, Fu F, Li R, Yang WQ, Liao HY, Yan JR, Li J, Li SY, Yang X, Li DZ. Liao C, et al. Eur J Med Genet. 2013 Sep;56(9):484-9. doi: 10.1016/j.ejmg.2013.06.008. Epub 2013 Jul 5. Eur J Med Genet. 2013. PMID: 23832105

2

Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.

Cacace R, Heeman B, Van Mossevelde S, De Roeck A, Hoogmartens J, De Rijk P, Gossye H, De Vos K, De Coster W, Strazisar M, De Baets G, Schymkowitz J, Rousseau F, Geerts N, De Pooter T, Peeters K, Sieben A, Martin JJ, Engelborghs S, Salmon E, Santens P, Vandenberghe R, Cras P, P De Deyn P, C van Swieten J, M van Duijn C, van der Zee J, Sleegers K, Van Broeckhoven C; BELNEU Consortium. Cacace R, et al. Acta Neuropathol. 2019 Jun;137(6):901-918. doi: 10.1007/s00401-019-01976-3. Epub 2019 Mar 14. Acta Neuropathol. 2019. PMID: 30874922 Free PMC article.

3

Combined deletion of two Condensin II system genes (NCAPG2 and MCPH1) in a case of severe microcephaly and mental deficiency.

Perche O, Menuet A, Marcos M, Liu L, Pâris A, Utami KH, Kervran D, Cacheux V, Laudier B, Briault S. Perche O, et al. Eur J Med Genet. 2013 Nov;56(11):635-41. doi: 10.1016/j.ejmg.2013.07.007. Epub 2013 Sep 4. Eur J Med Genet. 2013. PMID: 24013099

4

The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy.

Courcet JB, Faivre L, Malzac P, Masurel-Paulet A, Lopez E, Callier P, Lambert L, Lemesle M, Thevenon J, Gigot N, Duplomb L, Ragon C, Marle N, Mosca-Boidron AL, Huet F, Philippe C, Moncla A, Thauvin-Robinet C. Courcet JB, et al. J Med Genet. 2012 Dec;49(12):731-6. doi: 10.1136/jmedgenet-2012-101251. Epub 2012 Oct 25. J Med Genet. 2012. PMID: 23099646

5

DPP6 gene disruption in a family with Gilles de la Tourette syndrome.

Prontera P, Napolioni V, Ottaviani V, Rogaia D, Fusco C, Augello B, Serino D, Parisi V, Bernardini L, Merla G, Cavanna AE, Donti E. Prontera P, et al. Neurogenetics. 2014 Oct;15(4):237-42. doi: 10.1007/s10048-014-0418-9. Epub 2014 Aug 17. Neurogenetics. 2014. PMID: 25129042

6

Abnormal spindle-like microcephaly gene detection in an autosomal recessive microcephalic Saudi patient with attention deficit hyperactivity disorder and mental retardation.

Mahmoud AA, Siddiqui IA. Mahmoud AA, et al. Neurosciences (Riyadh). 2013 Jul;18(3):278-80. Neurosciences (Riyadh). 2013. PMID: 23887221 No abstract available.

7

Expression of DPP6 in Meckel's cartilage and tooth germs during mouse facial development.

Du J, Fan Z, Ma X, Wu Y, Liu S, Gao Y, Shen Y, Fan M, Wang S. Du J, et al. Biotech Histochem. 2014 Jan;89(1):14-8. doi: 10.3109/10520295.2013.795661. Epub 2013 Jun 10. Biotech Histochem. 2014. PMID: 23750656

8

Implication of LRRC4C and DPP6 in neurodevelopmental disorders.

Maussion G, Cruceanu C, Rosenfeld JA, Bell SC, Jollant F, Szatkiewicz J, Collins RL, Hanscom C, Kolobova I, de Champfleur NM, Blumenthal I, Chiang C, Ota V, Hultman C, O'Dushlaine C, McCarroll S, Alda M, Jacquemont S, Ordulu Z, Marshall CR, Carter MT, Shaffer LG, Sklar P, Girirajan S, Morton CC, Gusella JF, Turecki G, Stavropoulos DJ, Sullivan PF, Scherer SW, Talkowski ME, Ernst C. Maussion G, et al. Am J Med Genet A. 2017 Feb;173(2):395-406. doi: 10.1002/ajmg.a.38021. Epub 2016 Oct 19. Am J Med Genet A. 2017. PMID: 27759917 Free PMC article.

9

Autosomal dominant microcephaly without mental retardation.

Rossi LN, Candini G, Scarlatti G, Rossi G, Prina E, Alberti S. Rossi LN, et al. Am J Dis Child. 1987 Jun;141(6):655-9. doi: 10.1001/archpedi.1987.04460060071037. Am J Dis Child. 1987. PMID: 3578190

10

Mapping breakpoints of a familial chromosome insertion (18,7) (q22.1; q36.2q21.11) to DPP6 and CACNA2D1 genes in an azoospermic male.

Li L, Chen H, Yin C, Yang C, Wang B, Zheng S, Zhang J, Fan W. Li L, et al. Gene. 2014 Aug 15;547(1):43-9. doi: 10.1016/j.gene.2014.06.007. Epub 2014 Jun 14. Gene. 2014. PMID: 24937803

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