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Year Number of Results
2015 3
2016 5
2017 7
2018 7
2019 4
2020 4
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27 results
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Page 1
Genome sequencing in the clinic: the past, present, and future of genomic medicine.
Prokop JW, May T, Strong K, Bilinovich SM, Bupp C, Rajasekaran S, Worthey EA, Lazar J. Prokop JW, et al. Physiol Genomics. 2018 Aug 1;50(8):563-579. doi: 10.1152/physiolgenomics.00046.2018. Epub 2018 May 4. Physiol Genomics. 2018. PMID: 29727589 Free PMC article. Review.
De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder.
Snijders Blok L, Hiatt SM, Bowling KM, Prokop JW, Engel KL, Cochran JN, Bebin EM, Bijlsma EK, Ruivenkamp CAL, Terhal P, Simon MEH, Smith R, Hurst JA; DDD study, McLaughlin H, Person R, Crunk A, Wangler MF, Streff H, Symonds JD, Zuberi SM, Elliott KS, Sanders VR, Masunga A, Hopkin RJ, Dubbs HA, Ortiz-Gonzalez XR, Pfundt R, Brunner HG, Fisher SE, Kleefstra T, Cooper GM. Snijders Blok L, et al. Hum Genet. 2018 May;137(5):375-388. doi: 10.1007/s00439-018-1887-y. Epub 2018 May 8. Hum Genet. 2018. PMID: 29740699 Free PMC article.
Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.
Hiatt SM, Thompson ML, Prokop JW, Lawlor JMJ, Gray DE, Bebin EM, Rinne T, Kempers M, Pfundt R, van Bon BW, Mignot C, Nava C, Depienne C, Kalsner L, Rauch A, Joset P, Bachmann-Gagescu R, Wentzensen IM, McWalter K, Cooper GM. Hiatt SM, et al. Am J Hum Genet. 2019 Apr 4;104(4):701-708. doi: 10.1016/j.ajhg.2019.02.002. Epub 2019 Mar 14. Am J Hum Genet. 2019. PMID: 30879638 Free PMC article.
Characterization of Coding/Noncoding Variants for SHROOM3 in Patients with CKD.
Prokop JW, Yeo NC, Ottmann C, Chhetri SB, Florus KL, Ross EJ, Sosonkina N, Link BA, Freedman BI, Coppola CJ, McDermott-Roe C, Leysen S, Milroy LG, Meijer FA, Geurts AM, Rauscher FJ 3rd, Ramaker R, Flister MJ, Jacob HJ, Mendenhall EM, Lazar J. Prokop JW, et al. J Am Soc Nephrol. 2018 May;29(5):1525-1535. doi: 10.1681/ASN.2017080856. Epub 2018 Feb 23. J Am Soc Nephrol. 2018. PMID: 29476007 Free PMC article.
SARS-CoV-2 (COVID-19) structural and evolutionary dynamicome: Insights into functional evolution and human genomics.
Gupta R, Charron J, Stenger CL, Painter J, Steward H, Cook TW, Faber W, Frisch A, Lind E, Bauss J, Li X, Sirpilla O, Soehnlen X, Underwood A, Hinds D, Morris M, Lamb N, Carcillo JA, Bupp C, Uhal BD, Rajasekaran S, Prokop JW. Gupta R, et al. J Biol Chem. 2020 Aug 14;295(33):11742-11753. doi: 10.1074/jbc.RA120.014873. Epub 2020 Jun 25. J Biol Chem. 2020. PMID: 32587094 Free PMC article.
2015 Guidelines for Establishing Genetically Modified Rat Models for Cardiovascular Research.
Flister MJ, Prokop JW, Lazar J, Shimoyama M, Dwinell M, Geurts A; International Committee on Standardized Genetic Nomenclature for Mice; Rat Genome and Nomenclature Committee. Flister MJ, et al. J Cardiovasc Transl Res. 2015 Jun;8(4):269-77. doi: 10.1007/s12265-015-9626-4. Epub 2015 Apr 29. J Cardiovasc Transl Res. 2015. PMID: 25920443 Free PMC article. Review.
Functional domain analysis of SOX18 transcription factor using a single-chain variable fragment-based approach.
Fontaine FR, Goodall S, Prokop JW, Howard CB, Moustaqil M, Kumble S, Rasicci DT, Osborne GW, Gambin Y, Sierecki E, Jones ML, Zuegg J, Mahler S, Francois M. Fontaine FR, et al. MAbs. 2018 May/Jun;10(4):596-606. doi: 10.1080/19420862.2018.1451288. Epub 2018 Apr 16. MAbs. 2018. PMID: 29648920 Free PMC article.
HDAC2 Regulates Site-Specific Acetylation of MDM2 and Its Ubiquitination Signaling in Tumor Suppression.
Patel N, Wang J, Shiozawa K, Jones KB, Zhang Y, Prokop JW, Davenport GG, Nihira NT, Hao Z, Wong D, Brandsmeier L, Meadows SK, Sampaio AV, Werff RV, Endo M, Capecchi MR, McNagny KM, Mak TW, Nielsen TO, Underhill TM, Myers RM, Kondo T, Su L. Patel N, et al. iScience. 2019 Mar 29;13:43-54. doi: 10.1016/j.isci.2019.02.008. Epub 2019 Feb 15. iScience. 2019. PMID: 30818224 Free PMC article.
On the Molecular Evolution of Leptin, Leptin Receptor, and Endospanin.
Londraville RL, Prokop JW, Duff RJ, Liu Q, Tuttle M. Londraville RL, et al. Front Endocrinol (Lausanne). 2017 Apr 10;8:58. doi: 10.3389/fendo.2017.00058. eCollection 2017. Front Endocrinol (Lausanne). 2017. PMID: 28443063 Free PMC article.
Breakdown of multiple sclerosis genetics to identify an integrated disease network and potential variant mechanisms.
Shepard CJ, Cline SG, Hinds D, Jahanbakhsh S, Prokop JW. Shepard CJ, et al. Physiol Genomics. 2019 Nov 1;51(11):562-577. doi: 10.1152/physiolgenomics.00120.2018. Epub 2019 Sep 4. Physiol Genomics. 2019. PMID: 31482761 Free PMC article.
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