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Year Number of Results
2017 3
2018 3
2019 9
2020 3
2021 6
2022 1
2023 3
2024 1

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27 results

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Page 1
FTO variation and early frontostriatal brain development in children.
Thapaliya G, Kundu P, Jansen E, Naymik MA, Lee R, Bruchhage MMK, D'Sa V, Huentelman MJ, Lewis CR, Müller HG, Deoni SCL; RESONANCE consortium; Carnell S. Thapaliya G, et al. Among authors: naymik ma. Obesity (Silver Spring). 2024 Jan;32(1):156-165. doi: 10.1002/oby.23926. Epub 2023 Oct 10. Obesity (Silver Spring). 2024. PMID: 37817330
Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders.
Frankel E, Podder A, Sharifi M, Pillai R, Belnap N, Ramsey K, Dodson J, Venugopal P, Brzezinski M, Llaci L, Gerald B, Mills G, Sanchez-Castillo M, Balak CD, Szelinger S, Jepsen WM, Siniard AL, Richholt R, Naymik M, Schrauwen I, Craig DW, Piras IS, Huentelman MJ, Schork NJ, Narayanan V, Rangasamy S. Frankel E, et al. Among authors: naymik m. Cells. 2023 May 21;12(10):1437. doi: 10.3390/cells12101437. Cells. 2023. PMID: 37408271 Free PMC article.
Progressive cerebellar atrophy caused by heterozygous TECPR2 mutations.
Ramsey K, Belnap N, Bonfitto A, Jepsen W, Naymik M, Sanchez-Castillo M, Craig DW, Szelinger S, Huentelman MJ, Narayanan V, Rangasamy S. Ramsey K, et al. Among authors: naymik m. Mol Genet Genomic Med. 2022 Feb;10(2):e1857. doi: 10.1002/mgg3.1857. Epub 2022 Jan 7. Mol Genet Genomic Med. 2022. PMID: 34994087 Free PMC article. No abstract available.
Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases.
De La Vega FM, Chowdhury S, Moore B, Frise E, McCarthy J, Hernandez EJ, Wong T, James K, Guidugli L, Agrawal PB, Genetti CA, Brownstein CA, Beggs AH, Löscher BS, Franke A, Boone B, Levy SE, Õunap K, Pajusalu S, Huentelman M, Ramsey K, Naymik M, Narayanan V, Veeraraghavan N, Billings P, Reese MG, Yandell M, Kingsmore SF. De La Vega FM, et al. Among authors: naymik m. Genome Med. 2021 Oct 14;13(1):153. doi: 10.1186/s13073-021-00965-0. Genome Med. 2021. PMID: 34645491 Free PMC article.
Family SES Is Associated with the Gut Microbiome in Infants and Children.
Lewis CR, Bonham KS, McCann SH, Volpe AR, D'Sa V, Naymik M, De Both MD, Huentelman MJ, Lemery-Chalfant K, Highlander SK, Deoni SCL, Klepac-Ceraj V. Lewis CR, et al. Among authors: naymik m. Microorganisms. 2021 Jul 28;9(8):1608. doi: 10.3390/microorganisms9081608. Microorganisms. 2021. PMID: 34442687 Free PMC article.
DNA Methylation and Expression Profiles of Whole Blood in Parkinson's Disease.
Henderson AR, Wang Q, Meechoovet B, Siniard AL, Naymik M, De Both M, Huentelman MJ, Caselli RJ, Driver-Dunckley E, Dunckley T. Henderson AR, et al. Among authors: naymik m. Front Genet. 2021 Apr 26;12:640266. doi: 10.3389/fgene.2021.640266. eCollection 2021. Front Genet. 2021. PMID: 33981329 Free PMC article.
27 results