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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2015 | 2 |
2016 | 1 |
2020 | 1 |
2021 | 2 |
2022 | 2 |
2024 | 0 |
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7 results
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New discoveries in schizophrenia genetics reveal neurobiological pathways: A review of recent findings.
Eur J Med Genet. 2015 Dec;58(12):704-14. doi: 10.1016/j.ejmg.2015.10.008. Epub 2015 Oct 19.
Eur J Med Genet. 2015.
PMID: 26493318
Free PMC article.
Review.
Craniofacial features of 3q29 deletion syndrome: Application of next-generation phenotyping technology.
Mak BC, Sanchez Russo R, Gambello MJ, Fleischer N, Black ED, Leslie E, Murphy MM; Emory 3q29 Project; Mulle JG.
Mak BC, et al.
Am J Med Genet A. 2021 Jul;185(7):2094-2101. doi: 10.1002/ajmg.a.62227. Epub 2021 May 3.
Am J Med Genet A. 2021.
PMID: 33938623
Free PMC article.
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Novel features of 3q29 deletion syndrome: Results from the 3q29 registry.
Glassford MR, Rosenfeld JA, Freedman AA, Zwick ME, Mulle JG; Unique Rare Chromosome Disorder Support Group.
Glassford MR, et al.
Am J Med Genet A. 2016 Apr;170A(4):999-1006. doi: 10.1002/ajmg.a.37537. Epub 2016 Jan 6.
Am J Med Genet A. 2016.
PMID: 26738761
Free PMC article.
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Caregiver Perspectives on a Child's Diagnosis of 3q29 Deletion: "We Can't Just Wish This Thing Away".
Glassford MR, Purcell RH, Pass S, Murphy MM, Bassell GJ, Mulle JG; Emory 3q29 Project,*.
Glassford MR, et al.
J Dev Behav Pediatr. 2022 Feb-Mar 01;43(2):e94-e102. doi: 10.1097/DBP.0000000000000977.
J Dev Behav Pediatr. 2022.
PMID: 34320535
Free PMC article.
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Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
Cleynen I, Engchuan W, Hestand MS, Heung T, Holleman AM, Johnston HR, Monfeuga T, McDonald-McGinn DM, Gur RE, Morrow BE, Swillen A, Vorstman JAS, Bearden CE, Chow EWC, van den Bree M, Emanuel BS, Vermeesch JR, Warren ST, Owen MJ, Chopra P, Cutler DJ, Duncan R, Kotlar AV, Mulle JG, Voss AJ, Zwick ME, Diacou A, Golden A, Guo T, Lin JR, Wang T, Zhang Z, Zhao Y, Marshall C, Merico D, Jin A, Lilley B, Salmons HI, Tran O, Holmans P, Pardinas A, Walters JTR, Demaerel W, Boot E, Butcher NJ, Costain GA, Lowther C, Evers R, van Amelsvoort TAMJ, van Duin E, Vingerhoets C, Breckpot J, Devriendt K, Vergaelen E, Vogels A, Crowley TB, McGinn DE, Moss EM, Sharkus RJ, Unolt M, Zackai EH, Calkins ME, Gallagher RS, Gur RC, Tang SX, Fritsch R, Ornstein C, Repetto GM, Breetvelt E, Duijff SN, Fiksinski A, Moss H, Niarchou M, Murphy KC, Prasad SE, Daly EM, Gudbrandsen M, Murphy CM, Murphy DG, Buzzanca A, Fabio FD, Digilio MC, Pontillo M, Marino B, Vicari S, Coleman K, Cubells JF, Ousley OY, Carmel M, Gothelf D, Mekori-Domachevsky E, Michaelovsky E, Weinberger R, Weizman A, Kushan L, Jalbrzikowski M, Armando M, Eliez S, Sandini C, Schneider M, Béna FS, Antshel KM, Fremont W, Kates WR, Belzeaux R, Busa T,…
See abstract for full author list ➔
Cleynen I, et al.
Mol Psychiatry. 2021 Aug;26(8):4496-4510. doi: 10.1038/s41380-020-0654-3. Epub 2020 Feb 3.
Mol Psychiatry. 2021.
PMID: 32015465
Free PMC article.
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The 3q29 deletion confers >40-fold increase in risk for schizophrenia.
Mulle JG.
Mulle JG.
Mol Psychiatry. 2015 Sep;20(9):1028-9. doi: 10.1038/mp.2015.76. Epub 2015 Jun 9.
Mol Psychiatry. 2015.
PMID: 26055425
Free PMC article.
No abstract available.
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Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons.
Kozlova A, Zhang S, Kotlar AV, Jamison B, Zhang H, Shi S, Forrest MP, McDaid J, Cutler DJ, Epstein MP, Zwick ME, Pang ZP, Sanders AR, Warren ST, Gejman PV, Mulle JG, Duan J.
Kozlova A, et al.
Am J Hum Genet. 2022 Aug 4;109(8):1500-1519. doi: 10.1016/j.ajhg.2022.07.001.
Am J Hum Genet. 2022.
PMID: 35931052
Free PMC article.
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