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Year Number of Results
2015 2
2016 4
2017 6
2018 4
2019 4
2020 3
2021 3
2023 1
2024 0

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25 results

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Page 1
Exploring genome-wide DNA methylation patterns in Aicardi syndrome.
Piras IS, Mills G, Llaci L, Naymik M, Ramsey K, Belnap N, Balak CD, Jepsen WM, Szelinger S, Siniard AL, Lewis CR, LaFleur M, Richholt RF, De Both MD, Avela K, Rangasamy S, Craig DW, Narayanan V, Järvelä I, Huentelman MJ, Schrauwen I. Piras IS, et al. Among authors: richholt rf. Epigenomics. 2017 Nov;9(11):1373-1386. doi: 10.2217/epi-2017-0060. Epub 2017 Oct 2. Epigenomics. 2017. PMID: 28967789
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: richholt r. Cells. 2023 May 21;12(10):1437. doi: 10.3390/cells12101437. Cells. 2023. PMID: 37408271 Free PMC article.
Extracellular circular RNA profiles in plasma and urine of healthy, male college athletes.
Hutchins E, Reiman R, Winarta J, Beecroft T, Richholt R, De Both M, Shahbander K, Carlson E, Janss A, Siniard A, Balak C, Bruhns R, Whitsett TG, McCoy R, Anastasi M, Allen A, Churas B, Huentelman M, Van Keuren-Jensen K. Hutchins E, et al. Among authors: richholt r. Sci Data. 2021 Oct 28;8(1):276. doi: 10.1038/s41597-021-01056-w. Sci Data. 2021. PMID: 34711851 Free PMC article.
Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers.
Huentelman MJ, Piras IS, Siniard AL, De Both MD, Richholt RF, Balak CD, Jamshidi P, Bigio EH, Weintraub S, Loyer ET, Mesulam MM, Geula C, Rogalski EJ. Huentelman MJ, et al. Among authors: richholt rf. Front Aging Neurosci. 2018 May 29;10:155. doi: 10.3389/fnagi.2018.00155. eCollection 2018. Front Aging Neurosci. 2018. PMID: 29896098 Free PMC article.
Transcriptome-wide association study of post-trauma symptom trajectories identified GRIN3B as a potential biomarker for PTSD development.
Lori A, Schultebraucks K, Galatzer-Levy I, Daskalakis NP, Katrinli S, Smith AK, Myers AJ, Richholt R, Huentelman M, Guffanti G, Wuchty S, Gould F, Harvey PD, Nemeroff CB, Jovanovic T, Gerasimov ES, Maples-Keller JL, Stevens JS, Michopoulos V, Rothbaum BO, Wingo AP, Ressler KJ. Lori A, et al. Among authors: richholt r. Neuropsychopharmacology. 2021 Sep;46(10):1811-1820. doi: 10.1038/s41386-021-01073-8. Epub 2021 Jun 29. Neuropsychopharmacology. 2021. PMID: 34188182 Free PMC article.
Congenital myasthenic syndrome caused by a frameshift insertion mutation in GFPT1.
Szelinger S, Krate J, Ramsey K, Strom SP, Shieh PB, Lee H, Belnap N, Balak C, Siniard AL, Russell M, Richholt R, Both M, Claasen AM, Schrauwen I, Nelson SF, Huentelman MJ, Craig DW, Yang SP, Moore SA, Sivakumar K, Narayanan V, Rangasamy S; UCLA Clinical Genomics Center. Szelinger S, et al. Among authors: richholt r. Neurol Genet. 2020 Jun 30;6(4):e468. doi: 10.1212/NXG.0000000000000468. eCollection 2020 Aug. Neurol Genet. 2020. PMID: 32754643 Free PMC article.
Total Extracellular Small RNA Profiles from Plasma, Saliva, and Urine of Healthy Subjects.
Yeri A, Courtright A, Reiman R, Carlson E, Beecroft T, Janss A, Siniard A, Richholt R, Balak C, Rozowsky J, Kitchen R, Hutchins E, Winarta J, McCoy R, Anastasi M, Kim S, Huentelman M, Van Keuren-Jensen K. Yeri A, et al. Among authors: richholt r. Sci Rep. 2017 Mar 17;7:44061. doi: 10.1038/srep44061. Sci Rep. 2017. PMID: 28303895 Free PMC article.
25 results