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

Year Number of Results
1969 1
1972 1
1973 1
1974 1
1978 1
1980 1
1982 1
1987 1
1988 1
1989 1
1990 1
1991 1
1992 1
1993 1
1994 4
1995 1
1996 2
1997 1
1998 1
1999 3
2000 1
2002 2
2003 3
2005 2
2006 3
2007 7
2008 7
2009 5
2010 4
2011 1
2012 2
2016 1
2019 1
2021 1
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63 results
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Page 1
Intellectual functioning in alpha-mannosidosis.
Cathey SS, Sarasua SM, Simensen R, Pietris K, Kimbrell G, Sillence D, Wilson C, Horowitz L. Cathey SS, et al. Among authors: simensen r. JIMD Rep. 2019 Sep 21;50(1):44-49. doi: 10.1002/jmd2.12073. eCollection 2019 Nov. JIMD Rep. 2019. PMID: 31741826 Free PMC article.
Autistic Disorder: A 20 Year Chronicle.
Skinner C, Pauly R, Skinner SA, Schroer RJ, Simensen RJ, Taylor HA, Friez MJ, DuPont BR, Stevenson RE. Skinner C, et al. Among authors: simensen rj. J Autism Dev Disord. 2021 Feb;51(2):677-684. doi: 10.1007/s10803-020-04568-3. J Autism Dev Disord. 2021. PMID: 32592095
Autism and macrocephaly.
Stevenson RE, Schroer RJ, Skinner C, Fender D, Simensen RJ. Stevenson RE, et al. Among authors: simensen rj. Lancet. 1997 Jun 14;349(9067):1744-5. doi: 10.1016/S0140-6736(05)62956-X. Lancet. 1997. PMID: 9193390 No abstract available.
Finding new etiologies of mental retardation and hypotonia: X marks the spot.
Rogers RC, Stevenson RE, Simensen RJ, Holden KR, Schwartz CE. Rogers RC, et al. Among authors: simensen rj. Dev Med Child Neurol. 2008 Feb;50(2):104-11. doi: 10.1111/j.1469-8749.2007.02022.x. Epub 2008 Jan 7. Dev Med Child Neurol. 2008. PMID: 18190539 Free article. Review.
Natural history of Christianson syndrome.
Schroer RJ, Holden KR, Tarpey PS, Matheus MG, Griesemer DA, Friez MJ, Fan JZ, Simensen RJ, Strømme P, Stevenson RE, Stratton MR, Schwartz CE. Schroer RJ, et al. Among authors: simensen rj. Am J Med Genet A. 2010 Nov;152A(11):2775-83. doi: 10.1002/ajmg.a.33093. Am J Med Genet A. 2010. PMID: 20949524 Free PMC article.
Fragile-X syndrome.
Simensen RJ, Rogers RC. Simensen RJ, et al. Am Fam Physician. 1989 May;39(5):185-93. Am Fam Physician. 1989. PMID: 2655406 Review.
Cognitive function in Coffin-Lowry syndrome.
Simensen RJ, Abidi F, Collins JS, Schwartz CE, Stevenson RE. Simensen RJ, et al. Clin Genet. 2002 Apr;61(4):299-304. doi: 10.1034/j.1399-0004.2002.610410.x. Clin Genet. 2002. PMID: 12030896
Fragile-X syndrome.
Simensen RJ. Simensen RJ. Am Fam Physician. 1993 Apr;47(5):1072-3. Am Fam Physician. 1993. PMID: 8465704 No abstract available.
HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing study.
Friez MJ, Brooks SS, Stevenson RE, Field M, Basehore MJ, Adès LC, Sebold C, McGee S, Saxon S, Skinner C, Craig ME, Murray L, Simensen RJ, Yap YY, Shaw MA, Gardner A, Corbett M, Kumar R, Bosshard M, van Loon B, Tarpey PS, Abidi F, Gecz J, Schwartz CE. Friez MJ, et al. Among authors: simensen rj. BMJ Open. 2016 Apr 29;6(4):e009537. doi: 10.1136/bmjopen-2015-009537. BMJ Open. 2016. PMID: 27130160 Free PMC article.
63 results
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