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

Year Number of Results
1988 2
1993 1
1994 3
1995 2
1996 1
1997 1
1998 1
1999 4
2000 3
2001 3
2002 1
2003 3
2004 4
2005 1
2006 1
2007 3
2008 7
2009 16
2010 10
2011 5
2012 10
2013 11
2014 8
2015 7
2016 4
2017 3
2018 11
2019 5
2020 6
2021 3
2022 4
2023 1
2024 1

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131 results

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Page 1
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.
Rivière JB, Mirzaa GM, O'Roak BJ, Beddaoui M, Alcantara D, Conway RL, St-Onge J, Schwartzentruber JA, Gripp KW, Nikkel SM, Worthylake T, Sullivan CT, Ward TR, Butler HE, Kramer NA, Albrecht B, Armour CM, Armstrong L, Caluseriu O, Cytrynbaum C, Drolet BA, Innes AM, Lauzon JL, Lin AE, Mancini GM, Meschino WS, Reggin JD, Saggar AK, Lerman-Sagie T, Uyanik G, Weksberg R, Zirn B, Beaulieu CL; Finding of Rare Disease Genes (FORGE) Canada Consortium; Majewski J, Bulman DE, O'Driscoll M, Shendure J, Graham JM Jr, Boycott KM, Dobyns WB. Rivière JB, et al. Among authors: meschino ws. Nat Genet. 2012 Jun 24;44(8):934-40. doi: 10.1038/ng.2331. Nat Genet. 2012. PMID: 22729224 Free PMC article.
Genetics: Codeine metabolism.
Gibbons CA, Blaine SM, Allanson J, Cremin C, Dorman H, Honeywell C, Meschino WS, Permaul J, Carroll JC. Gibbons CA, et al. Among authors: meschino ws. Can Fam Physician. 2009 Feb;55(2):164. Can Fam Physician. 2009. PMID: 19221076 Free PMC article. No abstract available.
Genetics: schizophrenia.
Rideout AL, Carroll JC, Blaine SM, Cremin C, Dorman H, Gibbons CA, Honeywell C, Meschino WS, Permaul J, Allanson J. Rideout AL, et al. Among authors: meschino ws. Can Fam Physician. 2009 Dec;55(12):1207. Can Fam Physician. 2009. PMID: 20008600 Free PMC article. No abstract available.
Development and validation of a prognostic model to predict birth weight: individual participant data meta-analysis.
Allotey J, Archer L, Snell KIE, Coomar D, Massé J, Sletner L, Wolf H, Daskalakis G, Saito S, Ganzevoort W, Ohkuchi A, Mistry H, Farrar D, Mone F, Zhang J, Seed PT, Teede H, Da Silva Costa F, Souka AP, Smuk M, Ferrazzani S, Salvi S, Prefumo F, Gabbay-Benziv R, Nagata C, Takeda S, Sequeira E, Lapaire O, Cecatti JG, Morris RK, Baschat AA, Salvesen K, Smits L, Anggraini D, Rumbold A, van Gelder M, Coomarasamy A, Kingdom J, Heinonen S, Khalil A, Goffinet F, Haqnawaz S, Zamora J, Riley RD, Thangaratinam S; International Prediction of Pregnancy Complications collaborative network; Kwong A, Savitri AI, Bhattacharya S, Uiterwaal CS, Staff AC, Andersen LB, Olive EL, Redman C, Macleod M, Thilaganathan B, Ramírez JA, Audibert F, Magnus PM, Jenum AK, McAuliffe FM, West J, Askie LM, Zimmerman PA, Riddell C, van de Post J, Illanes SE, Holzman C, van Kuijk SMJ, Carbillon L, Villa PM, Eskild A, Chappell L, Velauthar L, van Oostwaard M, Verlohren S, Poston L, Ferrazzi E, Vinter CA, Brown M, Vollebregt KC, Langenveld J, Widmer M, Haavaldsen C, Carroli G, Olsen J, Zavaleta N, Eisensee I, Vergani P, Lumbiganon P, Makrides M, Facchinetti F, Temmerman M, Gibson R, Frusca T, Norman JE, Figueiró-Filho EA,… See abstract for full author list ➔ Allotey J, et al. Among authors: meschino ws. BMJ Med. 2024 Aug 14;3(1):e000784. doi: 10.1136/bmjmed-2023-000784. eCollection 2024. BMJ Med. 2024. PMID: 39184566 Free PMC article.
Genetics: familial melanoma.
Cremin C, Blaine SM, Allanson J, Dorman H, Gibbons CA, Honeywell C, Meschino WS, Permaul J, Carroll JC. Cremin C, et al. Among authors: meschino ws. Can Fam Physician. 2010 Jan;56(1):31. Can Fam Physician. 2010. PMID: 20090079 Free PMC article. No abstract available.
Genetics: Hypertrophic cardiomyopathy.
Honeywell C, Meschino WS, Allanson J, Blaine SM, Cremin C, Dorman H, Gibbons CA, Permaul J, Carroll JC. Honeywell C, et al. Among authors: meschino ws. Can Fam Physician. 2009 Nov;55(11):1095. Can Fam Physician. 2009. PMID: 19910596 Free PMC article. No abstract available.
Genetics: prostate cancer.
Blaine SM, Honeywell C, Allanson J, Cremin C, Dorman H, Gibbons CA, Meschino WS, Permaul J, Carroll JC. Blaine SM, et al. Among authors: meschino ws. Can Fam Physician. 2009 Jul;55(7):710. Can Fam Physician. 2009. PMID: 19602656 Free PMC article. No abstract available.
Genetics: hereditary hemochromatosis.
Allanson J, Honeywell C, Blaine SM, Cremin C, Dorman H, Gibbons CA, Grimshaw J, Meschino WS, Permaul J, Wilson BJ, Carroll JC. Allanson J, et al. Among authors: meschino ws. Can Fam Physician. 2009 Jan;55(1):53. Can Fam Physician. 2009. PMID: 19155369 Free PMC article. No abstract available.
De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature.
Nambot S, Faivre L, Mirzaa G, Thevenon J, Bruel AL, Mosca-Boidron AL, Masurel-Paulet A, Goldenberg A, Le Meur N, Charollais A, Mignot C, Petit F, Rossi M, Metreau J, Layet V, Amram D, Boute-Bénéjean O, Bhoj E, Cousin MA, Kruisselbrink TM, Lanpher BC, Klee EW, Fiala E, Grange DK, Meschino WS, Hiatt SM, Cooper GM, Olivié H, Smith WE, Dumas M, Lehman A; CAUSES Study; Inglese C, Nizon M, Guerrini R, Vetro A, Kaplan ES, Miramar D, Van Gils J, Fergelot P, Bodamer O, Herkert JC, Pajusalu S, Õunap K, Filiano JJ, Smol T, Piton A, Gérard B, Chantot-Bastaraud S, Bienvenu T, Li D, Juusola J, Devriendt K, Bilan F, Poé C, Chevarin M, Jouan T, Tisserant E, Rivière JB, Tran Mau-Them F, Philippe C, Duffourd Y, Dobyns WB, Hevner R, Thauvin-Robinet C. Nambot S, et al. Among authors: meschino ws. Eur J Hum Genet. 2020 Jun;28(6):770-782. doi: 10.1038/s41431-020-0571-6. Epub 2020 Jan 31. Eur J Hum Genet. 2020. PMID: 32005960 Free PMC article. Review.
131 results