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Results by year

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

Year Number of Results
1976 2
1977 1
1978 1
1980 2
1993 3
1994 4
1995 2
1996 2
1997 1
1998 3
1999 1
2001 1
2003 1
2007 2
2008 2
2009 1
2010 8
2011 5
2012 4
2013 5
2014 8
2015 4
2016 6
2017 8
2018 4
2019 1
2020 4
2021 5
2022 2
2023 2
2024 0

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81 results

Results by year

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Page 1
Cherubism.
Kannu P, Baskin B, Bowdin S. Kannu P, et al. Among authors: baskin b. 2007 Feb 26 [updated 2018 Nov 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2007 Feb 26 [updated 2018 Nov 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301316 Free Books & Documents. Review.
One Is Not Enough: Understanding and Modeling Polysubstance Use.
Crummy EA, O'Neal TJ, Baskin BM, Ferguson SM. Crummy EA, et al. Among authors: baskin bm. Front Neurosci. 2020 Jun 16;14:569. doi: 10.3389/fnins.2020.00569. eCollection 2020. Front Neurosci. 2020. PMID: 32612502 Free PMC article. Review.
X-linked agammaglobulinemia and other immunoglobulin deficiencies.
Smith CI, Islam KB, Vorechovský I, Olerup O, Wallin E, Rabbani H, Baskin B, Hammarström L. Smith CI, et al. Among authors: baskin b. Immunol Rev. 1994 Apr;138:159-83. doi: 10.1111/j.1600-065x.1994.tb00851.x. Immunol Rev. 1994. PMID: 8070814 Review. No abstract available.
Genetics of IgA deficiency.
Truedsson L, Baskin B, Pan Q, Rabbani H, Vorĕchovský I, Smith CI, Hammarström L. Truedsson L, et al. Among authors: baskin b. APMIS. 1995 Dec;103(12):833-42. doi: 10.1111/j.1699-0463.1995.tb01442.x. APMIS. 1995. PMID: 8562023 Review.
Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes.
Martinelli S, Krumbach OHF, Pantaleoni F, Coppola S, Amin E, Pannone L, Nouri K, Farina L, Dvorsky R, Lepri F, Buchholzer M, Konopatzki R, Walsh L, Payne K, Pierpont ME, Vergano SS, Langley KG, Larsen D, Farwell KD, Tang S, Mroske C, Gallotta I, Di Schiavi E, Della Monica M, Lugli L, Rossi C, Seri M, Cocchi G, Henderson L, Baskin B, Alders M, Mendoza-Londono R, Dupuis L, Nickerson DA, Chong JX; University of Washington Center for Mendelian Genomics; Meeks N, Brown K, Causey T, Cho MT, Demuth S, Digilio MC, Gelb BD, Bamshad MJ, Zenker M, Ahmadian MR, Hennekam RC, Tartaglia M, Mirzaa GM. Martinelli S, et al. Among authors: baskin b. Am J Hum Genet. 2018 Feb 1;102(2):309-320. doi: 10.1016/j.ajhg.2017.12.015. Epub 2018 Jan 25. Am J Hum Genet. 2018. PMID: 29394990 Free PMC article.
De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy.
Djordjevic D, Pinard M, Gauthier MS, Smith-Hicks C, Hoffman TL, Wolf NI, Oegema R, van Binsbergen E, Baskin B, Bernard G, Fribourg S, Coulombe B, Yoon G. Djordjevic D, et al. Among authors: baskin b. Am J Hum Genet. 2021 Jan 7;108(1):186-193. doi: 10.1016/j.ajhg.2020.12.002. Am J Hum Genet. 2021. PMID: 33417887 Free PMC article.
De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy.
Djordjevic D, Pinard M, Gauthier MS, Smith-Hicks C, Hoffman TL, Wolf NI, Oegema R, van Binsbergen E, Baskin B, Bernard G, Fribourg S, Coulombe B, Yoon G. Djordjevic D, et al. Among authors: baskin b. Am J Hum Genet. 2022 Apr 7;109(4):759-763. doi: 10.1016/j.ajhg.2022.03.006. Am J Hum Genet. 2022. PMID: 35395209 Free PMC article. No abstract available.
81 results