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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2001 | 1 |
2010 | 1 |
2011 | 1 |
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2015 | 2 |
2016 | 1 |
2021 | 1 |
2024 | 0 |
PubMed (cited) for id: 616327
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Neurodevelopmental phenotypes in individuals with pathogenic variants in CHAMP1.
Cold Spring Harb Mol Case Stud. 2021 Aug 2;7(4):a006092. doi: 10.1101/mcs.a006092. Print 2021 Aug.
Cold Spring Harb Mol Case Stud. 2021.
PMID: 34021018
Free PMC article.
De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment Gene CHAMP1 Cause Syndromic Intellectual Disability.
Isidor B, Küry S, Rosenfeld JA, Besnard T, Schmitt S, Joss S, Davies SJ, Lebel RR, Henderson A, Schaaf CP, Streff HE, Yang Y, Jain V, Chida N, Latypova X, Le Caignec C, Cogné B, Mercier S, Vincent M, Colin E, Bonneau D, Denommé AS, Parent P, Gilbert-Dussardier B, Odent S, Toutain A, Piton A, Dina C, Donnart A, Lindenbaum P, Charpentier E, Redon R, Iemura K, Ikeda M, Tanaka K, Bézieau S.
Isidor B, et al.
Hum Mutat. 2016 Apr;37(4):354-8. doi: 10.1002/humu.22952. Epub 2016 Feb 4.
Hum Mutat. 2016.
PMID: 26751395
Free article.
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De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment.
Hempel M, Cremer K, Ockeloen CW, Lichtenbelt KD, Herkert JC, Denecke J, Haack TB, Zink AM, Becker J, Wohlleber E, Johannsen J, Alhaddad B, Pfundt R, Fuchs S, Wieczorek D, Strom TM, van Gassen KL, Kleefstra T, Kubisch C, Engels H, Lessel D.
Hempel M, et al.
Am J Hum Genet. 2015 Sep 3;97(3):493-500. doi: 10.1016/j.ajhg.2015.08.003.
Am J Hum Genet. 2015.
PMID: 26340335
Free PMC article.
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Large-scale discovery of novel genetic causes of developmental disorders.
Deciphering Developmental Disorders Study.
Deciphering Developmental Disorders Study.
Nature. 2015 Mar 12;519(7542):223-8. doi: 10.1038/nature14135. Epub 2014 Dec 24.
Nature. 2015.
PMID: 25533962
Free PMC article.
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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Rauch A, Wieczorek D, Graf E, Wieland T, Endele S, Schwarzmayr T, Albrecht B, Bartholdi D, Beygo J, Di Donato N, Dufke A, Cremer K, Hempel M, Horn D, Hoyer J, Joset P, Röpke A, Moog U, Riess A, Thiel CT, Tzschach A, Wiesener A, Wohlleber E, Zweier C, Ekici AB, Zink AM, Rump A, Meisinger C, Grallert H, Sticht H, Schenck A, Engels H, Rappold G, Schröck E, Wieacker P, Riess O, Meitinger T, Reis A, Strom TM.
Rauch A, et al.
Lancet. 2012 Nov 10;380(9854):1674-82. doi: 10.1016/S0140-6736(12)61480-9. Epub 2012 Sep 27.
Lancet. 2012.
PMID: 23020937
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CAMP (C13orf8, ZNF828) is a novel regulator of kinetochore-microtubule attachment.
Itoh G, Kanno S, Uchida KS, Chiba S, Sugino S, Watanabe K, Mizuno K, Yasui A, Hirota T, Tanaka K.
Itoh G, et al.
EMBO J. 2011 Jan 5;30(1):130-44. doi: 10.1038/emboj.2010.276. Epub 2010 Nov 9.
EMBO J. 2011.
PMID: 21063390
Free PMC article.
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Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
Nagase T, Nakayama M, Nakajima D, Kikuno R, Ohara O.
Nagase T, et al.
DNA Res. 2001 Apr 27;8(2):85-95. doi: 10.1093/dnares/8.2.85.
DNA Res. 2001.
PMID: 11347906
Free article.
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