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For: Martin CL, Wain KE, Oetjens MT, Tolwinski K, Palen E, Hare-Harris A, Habegger L, Maxwell EK, Reid JG, Walsh LK, Myers SM, Ledbetter DH. Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population. JAMA Psychiatry 2020;77:1276-85. [PMID: 32697297 DOI: 10.1001/jamapsychiatry.2020.2159] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 7.0] [Reference Citation Analysis]
Number Citing Articles
1 Finucane BM, Ledbetter DH, Vorstman JA. Diagnostic genetic testing for neurodevelopmental psychiatric disorders: closing the gap between recommendation and clinical implementation. Curr Opin Genet Dev 2021;68:1-8. [PMID: 33434711 DOI: 10.1016/j.gde.2020.12.016] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
2 Auwerx C, Lepamets M, Sadler MC, Patxot M, Stojanov M, Baud D, Mägi R, Porcu E, Reymond A, Kutalik Z; Estonian Biobank Research Team. The individual and global impact of copy-number variants on complex human traits. Am J Hum Genet 2022:S0002-9297(22)00061-1. [PMID: 35240056 DOI: 10.1016/j.ajhg.2022.02.010] [Reference Citation Analysis]
3 Cheng MC, Chien WH, Huang YS, Fang TH, Chen CH. Translational Study of Copy Number Variations in Schizophrenia. Int J Mol Sci 2021;23:457. [PMID: 35008879 DOI: 10.3390/ijms23010457] [Reference Citation Analysis]
4 Mulle JG, Sullivan PF, Hjerling-Leffler J. Editorial overview: Rare CNV disorders and neuropsychiatric phenotypes: opportunities, challenges, solutions. Curr Opin Genet Dev 2021;68:iii-ix. [PMID: 34059379 DOI: 10.1016/j.gde.2021.05.002] [Reference Citation Analysis]
5 Cable J, Purcell RH, Robinson E, Vorstman JAS, Chung WK, Constantino JN, Sanders SJ, Sahin M, Dolmetsch RE, Shah BM, Thurm A, Martin CL, Bearden CE, Mulle JG. Harnessing rare variants in neuropsychiatric and neurodevelopment disorders-a Keystone Symposia report. Ann N Y Acad Sci 2021. [PMID: 34342000 DOI: 10.1111/nyas.14658] [Reference Citation Analysis]
6 Birnbaum R, Mahjani B, Loos RJF, Sharp AJ. Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry Biobank. JAMA Psychiatry 2022. [PMID: 35080590 DOI: 10.1001/jamapsychiatry.2021.4080] [Reference Citation Analysis]
7 Chawner SJ, Watson CJ, Owen MJ. Clinical evaluation of patients with a neuropsychiatric risk copy number variant. Curr Opin Genet Dev 2021;68:26-34. [PMID: 33461126 DOI: 10.1016/j.gde.2020.12.012] [Reference Citation Analysis]
8 Rees E, Kirov G. Copy number variation and neuropsychiatric illness. Curr Opin Genet Dev 2021;68:57-63. [PMID: 33752146 DOI: 10.1016/j.gde.2021.02.014] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
9 Silver A, Lazarin GA, Silver M, Miller M, Jansen M, Wechsberg C, Dekanek E, Grossfeld S, Herpel T, Gunatilake D, Bisignano A, Jaremko M. Technical Performance of a 430-Gene Preventative Genomics Assay to Identify Multiple Variant Types Associated with Adult-Onset Monogenic Conditions, Susceptibility Loci, and Pharmacogenetic Insights. JPM 2022;12:667. [DOI: 10.3390/jpm12050667] [Reference Citation Analysis]
10 Mortillo M, Mulle JG. A cross-comparison of cognitive ability across 8 genomic disorders. Curr Opin Genet Dev 2021;68:106-16. [PMID: 34082144 DOI: 10.1016/j.gde.2021.04.001] [Reference Citation Analysis]
11 Wainberg M, Merico D, Huguet G, Zarrei M, Jacquemont S, Scherer SW, Tripathy SJ. Deletion of Loss-of-Function-Intolerant Genes and Risk of 5 Psychiatric Disorders. JAMA Psychiatry 2021. [PMID: 34851367 DOI: 10.1001/jamapsychiatry.2021.3211] [Reference Citation Analysis]
12 Vorstman J, Scherer SW. What a finding of gene copy number variation can add to the diagnosis of developmental neuropsychiatric disorders. Curr Opin Genet Dev 2021;68:18-25. [PMID: 33454514 DOI: 10.1016/j.gde.2020.12.017] [Reference Citation Analysis]
13 Wain KE, Tolwinski K, Palen E, Heidlebaugh AR, Holdren K, Walsh LK, Oetjens MT, Ledbetter DH, Martin CL. Population Genomic Screening for Genetic Etiologies of Neurodevelopmental/Psychiatric Disorders Demonstrates Personal Utility and Positive Participant Responses. J Pers Med 2021;11:365. [PMID: 34062946 DOI: 10.3390/jpm11050365] [Reference Citation Analysis]
14 Finucane B, Oetjens MT, Johns A, Myers SM, Fisher C, Habegger L, Maxwell EK, Reid JG, Ledbetter DH, Kirchner HL, Martin CL. Medical manifestations and health care utilization among adult MyCode participants with neurodevelopmental psychiatric copy number variants. Genet Med 2021:S1098-3600(21)05388-0. [PMID: 34906480 DOI: 10.1016/j.gim.2021.11.010] [Reference Citation Analysis]
15 Kushima I, Nakatochi M, Aleksic B, Okada T, Kimura H, Kato H, Morikawa M, Inada T, Ishizuka K, Torii Y, Nakamura Y, Tanaka S, Imaeda M, Takahashi N, Yamamoto M, Iwamoto K, Nawa Y, Ogawa N, Iritani S, Hayashi Y, Lo T, Otgonbayar G, Furuta S, Iwata N, Ikeda M, Saito T, Ninomiya K, Okochi T, Hashimoto R, Yamamori H, Yasuda Y, Fujimoto M, Miura K, Itokawa M, Arai M, Miyashita M, Toriumi K, Ohi K, Shioiri T, Kitaichi K, Someya T, Watanabe Y, Egawa J, Takahashi T, Suzuki M, Sasaki T, Tochigi M, Nishimura F, Yamasue H, Kuwabara H, Wakuda T, Kato TA, Kanba S, Horikawa H, Usami M, Kodaira M, Watanabe K, Yoshikawa T, Toyota T, Yokoyama S, Munesue T, Kimura R, Funabiki Y, Kosaka H, Jung M, Kasai K, Ikegame T, Jinde S, Numata S, Kinoshita M, Kato T, Kakiuchi C, Yamakawa K, Suzuki T, Hashimoto N, Ishikawa S, Yamagata B, Nio S, Murai T, Son S, Kunii Y, Yabe H, Inagaki M, Goto Y, Okumura Y, Ito T, Arioka Y, Mori D, Ozaki N. Cross-disorder analysis of genic and regulatory copy number variations in bipolar disorder, schizophrenia, and autism spectrum disorder. Biological Psychiatry 2022. [DOI: 10.1016/j.biopsych.2022.04.003] [Reference Citation Analysis]
16 White LK, Crowley TB, Finucane B, Garcia‐minaur S, Repetto GM, Bree M, Fischer M, Jacquemont S, Barzilay R, Maillard AM, Donald KA, Gur RE, Bassett AS, Swillen A, Mcdonald‐mcginn DM. The COVID‐19 pandemic's impact on worry and medical disruptions reported by individuals with chromosome 22q11.2 copy number variants and their caregivers. J intellect Disabil Res. [DOI: 10.1111/jir.12918] [Reference Citation Analysis]
17 van Calker D, Serchov T. The "missing heritability"-Problem in psychiatry: Is the interaction of genetics, epigenetics and transposable elements a potential solution? Neurosci Biobehav Rev 2021;126:23-42. [PMID: 33757815 DOI: 10.1016/j.neubiorev.2021.03.019] [Reference Citation Analysis]
18 Adams RL, Baird A, Smith J, Williams N, van den Bree MBM, Linden DEJ, Owen MJ, Hall J, Linden SC. Psychopathology in adults with copy number variants. Psychol Med 2022;:1-8. [PMID: 35144709 DOI: 10.1017/S0033291721005201] [Reference Citation Analysis]
19 Dinneen TJ, Ghrálaigh FN, Walsh R, Lopez LM, Gallagher L. How does genetic variation modify ND-CNV phenotypes? Trends Genet 2021:S0168-9525(21)00196-7. [PMID: 34364706 DOI: 10.1016/j.tig.2021.07.006] [Reference Citation Analysis]
20 Pös O, Radvanszky J, Styk J, Pös Z, Buglyó G, Kajsik M, Budis J, Nagy B, Szemes T. Copy Number Variation: Methods and Clinical Applications. Applied Sciences 2021;11:819. [DOI: 10.3390/app11020819] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
21 Kelly MA, Leader JB, Wain KE, Bodian D, Oetjens MT, Ledbetter DH, Martin CL, Strande NT. Leveraging population-based exome screening to impact clinical care: The evolution of variant assessment in the Geisinger MyCode research project. Am J Med Genet C Semin Med Genet 2021;187:83-94. [PMID: 33576083 DOI: 10.1002/ajmg.c.31887] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Richter LD, Morley TJ, Hooker GW, Peay HL, Cox NJ, Ruderfer DM. Leveraging electronic health records to inform genetic counseling practice surrounding psychiatric disorders. J Genet Couns 2022. [PMID: 35191121 DOI: 10.1002/jgc4.1565] [Reference Citation Analysis]