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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2005 1
2007 1
2008 2
2010 3
2013 1
2014 1
2015 1
2016 2
2017 2
2018 6
2019 2
2020 1
2021 3
2022 2
2023 1
2024 1

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26 results

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Page 1
Muscle-derived factors influencing bone metabolism.
Gries KJ, Zysik VS, Jobe TK, Griffin N, Leeds BP, Lowery JW. Gries KJ, et al. Among authors: griffin n. Semin Cell Dev Biol. 2022 Mar;123:57-63. doi: 10.1016/j.semcdb.2021.10.009. Epub 2021 Oct 30. Semin Cell Dev Biol. 2022. PMID: 34756782 Review.
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature.
Hemati P, Revah-Politi A, Bassan H, Petrovski S, Bilancia CG, Ramsey K, Griffin NG, Bier L, Cho MT, Rosello M, Lynch SA, Colombo S, Weber A, Haug M, Heinzen EL, Sands TT, Narayanan V, Primiano M, Aggarwal VS, Millan F, Sattler-Holtrop SG, Caro-Llopis A, Pillar N, Baker J, Freedman R, Kroes HY, Sacharow S, Stong N, Lapunzina P, Schneider MC, Mendelsohn NJ, Singleton A, Loik Ramey V, Wou K, Kuzminsky A, Monfort S, Weiss M, Doyle S, Iglesias A, Martinez F, Mckenzie F, Orellana C, van Gassen KLI, Palomares M, Bazak L, Lee A, Bircher A, Basel-Vanagaite L, Hafström M, Houge G; C4RCD Research Group; DDD study; Goldstein DB, Anyane-Yeboa K. Hemati P, et al. Among authors: griffin ng. Am J Med Genet A. 2018 Nov;176(11):2259-2275. doi: 10.1002/ajmg.a.40472. Epub 2018 Sep 8. Am J Med Genet A. 2018. PMID: 30194818 Review.
NMUR1 in the NMU-Mediated Regulation of Bone Remodeling.
Hsiao YT, Manikowski KJ, Snyder S, Griffin N, Orr AL, Hulsey EQ, Born-Evers G, Zukosky T, Squire ME, Hum JM, Metzger CE, Allen MR, Lowery JW. Hsiao YT, et al. Among authors: griffin n. Life (Basel). 2021 Sep 29;11(10):1028. doi: 10.3390/life11101028. Life (Basel). 2021. PMID: 34685399 Free PMC article.
Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions.
Green TE, Motelow JE, Bennett MF, Ye Z, Bennett CA, Griffin NG, Damiano JA, Leventer RJ, Freeman JL, Harvey AS, Lockhart PJ, Sadleir LG, Boys A, Scheffer IE, Major H, Darbro BW, Bahlo M, Goldstein DB, Kerrigan JF, Heinzen EL, Berkovic SF, Hildebrand MS. Green TE, et al. Among authors: griffin ng. Hum Mol Genet. 2022 Jul 21;31(14):2307-2316. doi: 10.1093/hmg/ddab366. Hum Mol Genet. 2022. PMID: 35137044 Free PMC article.
Scapular anatomy of Paranthropus boisei from Ileret, Kenya.
Green DJ, Chirchir H, Mbua E, Harris JWK, Braun DR, Griffin NL, Richmond BG. Green DJ, et al. Among authors: griffin nl. J Hum Evol. 2018 Dec;125:181-192. doi: 10.1016/j.jhevol.2017.06.013. J Hum Evol. 2018. PMID: 30502893
Somatic uniparental disomy of Chromosome 16p in hemimegalencephaly.
Griffin NG, Cronin KD, Walley NM, Hulette CM, Grant GA, Mikati MA, LaBreche HG, Rehder CW, Allen AS, Crino PB, Heinzen EL. Griffin NG, et al. Cold Spring Harb Mol Case Stud. 2017 Sep 1;3(5):a001735. doi: 10.1101/mcs.a001735. Print 2017 Sep. Cold Spring Harb Mol Case Stud. 2017. PMID: 28864461 Free PMC article.
Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy.
Winawer MR, Griffin NG, Samanamud J, Baugh EH, Rathakrishnan D, Ramalingam S, Zagzag D, Schevon CA, Dugan P, Hegde M, Sheth SA, McKhann GM, Doyle WK, Grant GA, Porter BE, Mikati MA, Muh CR, Malone CD, Bergin AMR, Peters JM, McBrian DK, Pack AM, Akman CI, LaCoursiere CM, Keever KM, Madsen JR, Yang E, Lidov HGW, Shain C, Allen AS, Canoll PD, Crino PB, Poduri AH, Heinzen EL. Winawer MR, et al. Among authors: griffin ng. Ann Neurol. 2018 Jun;83(6):1133-1146. doi: 10.1002/ana.25243. Epub 2018 May 16. Ann Neurol. 2018. PMID: 29679388 Free PMC article.
26 results