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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2013 18
2014 12
2015 6
2016 9
2017 10
2018 8
2019 9
2020 7
2021 8
2022 6
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78 results
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Page 1
Identification of novel candidate disease genes from de novo exonic copy number variants.
Gambin T, Yuan B, Bi W, Liu P, Rosenfeld JA, Coban-Akdemir Z, Pursley AN, Nagamani SCS, Marom R, Golla S, Dengle L, Petrie HG, Matalon R, Emrick L, Proud MB, Treadwell-Deering D, Chao HT, Koillinen H, Brown C, Urraca N, Mostafavi R, Bernes S, Roeder ER, Nugent KM, Bader PI, Bellus G, Cummings M, Northrup H, Ashfaq M, Westman R, Wildin R, Beck AE, Immken L, Elton L, Varghese S, Buchanan E, Faivre L, Lefebvre M, Schaaf CP, Walkiewicz M, Yang Y, Kang SL, Lalani SR, Bacino CA, Beaudet AL, Breman AM, Smith JL, Cheung SW, Lupski JR, Patel A, Shaw CA, Stankiewicz P. Gambin T, et al. Genome Med. 2017 Sep 21;9(1):83. doi: 10.1186/s13073-017-0472-7. Genome Med. 2017. PMID: 28934986 Free PMC article.
Genetic study of NRXN1β variants in Spanish patients with schizophrenia.
Abasolo N, Roig B, Martorell L, Martínez-Leal R, Aguilera F, Camacho-García RJ, Orejuela C, Scholl FG, Martinez-Mir A, Vilella E. Abasolo N, et al. Schizophr Res. 2014 Nov;159(2-3):554-5. doi: 10.1016/j.schres.2014.09.002. Epub 2014 Sep 18. Schizophr Res. 2014. PMID: 25242362 No abstract available.
Genetic causes of developmental disorders.
Vorstman JA, Ophoff RA. Vorstman JA, et al. Curr Opin Neurol. 2013 Apr;26(2):128-36. doi: 10.1097/WCO.0b013e32835f1a30. Curr Opin Neurol. 2013. PMID: 23429547 Review.
NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.
Alliey-Rodriguez N, Grey TA, Shafee R, Asif H, Lutz O, Bolo NR, Padmanabhan J, Tandon N, Klinger M, Reis K, Spring J, Coppes L, Zeng V, Hegde RR, Hoang DT, Bannai D, Nawaz U, Henson P, Liu S, Gage D, McCarroll S, Bishop JR, Hill S, Reilly JL, Lencer R, Clementz BA, Buckley P, Glahn DC, Meda SA, Narayanan B, Pearlson G, Keshavan MS, Ivleva EI, Tamminga C, Sweeney JA, Curtis D, Badner JA, Keedy S, Rapoport J, Liu C, Gershon ES. Alliey-Rodriguez N, et al. Transl Psychiatry. 2019 Sep 17;9(1):230. doi: 10.1038/s41398-019-0564-9. Transl Psychiatry. 2019. PMID: 31530798 Free PMC article.
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.
Lowther C, Speevak M, Armour CM, Goh ES, Graham GE, Li C, Zeesman S, Nowaczyk MJ, Schultz LA, Morra A, Nicolson R, Bikangaga P, Samdup D, Zaazou M, Boyd K, Jung JH, Siu V, Rajguru M, Goobie S, Tarnopolsky MA, Prasad C, Dick PT, Hussain AS, Walinga M, Reijenga RG, Gazzellone M, Lionel AC, Marshall CR, Scherer SW, Stavropoulos DJ, McCready E, Bassett AS. Lowther C, et al. Genet Med. 2017 Jan;19(1):53-61. doi: 10.1038/gim.2016.54. Epub 2016 May 19. Genet Med. 2017. PMID: 27195815 Free PMC article.
78 results