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Showing results for christi. Wright
Search for Chris I. Wright instead (1 results)
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, De Vries BBA, Vissers LELM, Nordenskjold M, Kvarnung M, Lindstrand A, Nordgren A, Gecz J, Iascone M, Cereda A, Scatigno A, Maitz S, Zanni G, Bertini E, Zweier C, Schuhmann S, Wiesener A, Pepper M, Panjwani H, Torti E, Abid F, Anselm I, Srivastava S, Atwal P, Bacino CA, Bhat G, Cobian K, Bird LM, Friedman J, Wright MS, Callewaert B, Petit F, Mathieu S, Afenjar A, Christensen CK, White KM, Elpeleg O, Berger I, Espineli EJ, Fagerberg C, Brasch-Andersen C, Hansen LK, Feyma T, Hughes S, Thiffault I, Sullivan B, Yan S, Keller K, Keren B, Mignot C, Kooy F, Meuwissen M, Basinger A, Kukolich M, Philips M, Ortega L, Drummond-Borg M, Lauridsen M, Sorensen K, Lehman A; CAUSES Study; Lopez-Rangel E, Levy P, Lessel D, Lotze T, Madan-Khetarpal S, Sebastian J, Vento J, Vats D, Benman LM, Mckee S, Mirzaa GM, Muss C, Pappas J, Peeters H, Romano C, Elia M, Galesi O, Simon MEH, van Gassen KLI, Simpson K, Stratton R, Syed S, Thevenon J, Palafoll IV, Vitobello A, Bournez M, Faivre L, Xia K; SPARK Consortium; Earl RK, Nowakowski T, Bernier RA, Eichler EE. Gillentine MA, et al. Genome Med. 2021 Apr 19;13(1):63. doi: 10.1186/s13073-021-00870-6. Genome Med. 2021. PMID: 33874999 Free PMC article.
Defining and Scoping Participatory Health Informatics: An eDelphi Study.
Denecke K, Romero OR, Petersen C, Benham-Hutchins M, Cabrer M, Davies S, Grainger R, Hussein R, Lopez-Campos G, Martin-Sanchez F, McKillop M, Merolli M, Miron-Shatz T, Trigo JD, Wright G, Wynn R, Hullin Lucay Cossio C, Gabarron E. Denecke K, et al. Methods Inf Med. 2023 Sep;62(3-04):90-99. doi: 10.1055/a-2035-3008. Epub 2023 Feb 14. Methods Inf Med. 2023. PMID: 36787885 Free PMC article.
Diving into the vertical dimension of elasmobranch movement ecology.
Andrzejaczek S, Lucas TCD, Goodman MC, Hussey NE, Armstrong AJ, Carlisle A, Coffey DM, Gleiss AC, Huveneers C, Jacoby DMP, Meekan MG, Mourier J, Peel LR, Abrantes K, Afonso AS, Ajemian MJ, Anderson BN, Anderson SD, Araujo G, Armstrong AO, Bach P, Barnett A, Bennett MB, Bezerra NA, Bonfil R, Boustany AM, Bowlby HD, Branco I, Braun CD, Brooks EJ, Brown J, Burke PJ, Butcher P, Castleton M, Chapple TK, Chateau O, Clarke M, Coelho R, Cortes E, Couturier LIE, Cowley PD, Croll DA, Cuevas JM, Curtis TH, Dagorn L, Dale JJ, Daly R, Dewar H, Doherty PD, Domingo A, Dove ADM, Drew M, Dudgeon CL, Duffy CAJ, Elliott RG, Ellis JR, Erdmann MV, Farrugia TJ, Ferreira LC, Ferretti F, Filmalter JD, Finucci B, Fischer C, Fitzpatrick R, Forget F, Forsberg K, Francis MP, Franks BR, Gallagher AJ, Galvan-Magana F, García ML, Gaston TF, Gillanders BM, Gollock MJ, Green JR, Green S, Griffiths CA, Hammerschlag N, Hasan A, Hawkes LA, Hazin F, Heard M, Hearn A, Hedges KJ, Henderson SM, Holdsworth J, Holland KN, Howey LA, Hueter RE, Humphries NE, Hutchinson M, Jaine FRA, Jorgensen SJ, Kanive PE, Labaja J, Lana FO, Lassauce H, Lipscombe RS, Llewellyn F, Macena BCL, Mambrasar R, McAllister JD, McCully Phillips SR,… See abstract for full author list ➔ Andrzejaczek S, et al. Sci Adv. 2022 Aug 19;8(33):eabo1754. doi: 10.1126/sciadv.abo1754. Epub 2022 Aug 19. Sci Adv. 2022. PMID: 35984887 Free PMC article.
Internal validation of STRmix™ - A multi laboratory response to PCAST.
Bright JA, Richards R, Kruijver M, Kelly H, McGovern C, Magee A, McWhorter A, Ciecko A, Peck B, Baumgartner C, Buettner C, McWilliams S, McKenna C, Gallacher C, Mallinder B, Wright D, Johnson D, Catella D, Lien E, O'Connor C, Duncan G, Bundy J, Echard J, Lowe J, Stewart J, Corrado K, Gentile S, Kaplan M, Hassler M, McDonald N, Hulme P, Oefelein RH, Montpetit S, Strong M, Noël S, Malsom S, Myers S, Welti S, Moretti T, McMahon T, Grill T, Kalafut T, Greer-Ritzheimer M, Beamer V, Taylor DA, Buckleton JS. Bright JA, et al. Forensic Sci Int Genet. 2018 May;34:11-24. doi: 10.1016/j.fsigen.2018.01.003. Epub 2018 Jan 8. Forensic Sci Int Genet. 2018. PMID: 29367014
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