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Results by year

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
1993 1
1994 2
1995 1
1997 1
1998 1
1999 1
2000 1
2002 2
2003 3
2005 2
2006 2
2007 6
2008 4
2009 4
2010 2
2012 1
2016 1
2021 1
2023 0

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46 results

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Page 1
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.
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.
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.
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.
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
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.
Allan-Herndon syndrome. I. Clinical studies.
Stevenson RE, Goodman HO, Schwartz CE, Simensen RJ, McLean WT Jr, Herndon CN. Stevenson RE, et al. Among authors: simensen rj. Am J Hum Genet. 1990 Sep;47(3):446-53. Am J Hum Genet. 1990. PMID: 2393019 Free PMC article.
Renpenning syndrome comes into focus.
Stevenson RE, Bennett CW, Abidi F, Kleefstra T, Porteous M, Simensen RJ, Lubs HA, Hamel BC, Schwartz CE. Stevenson RE, et al. Among authors: simensen rj. Am J Med Genet A. 2005 May 1;134(4):415-21. doi: 10.1002/ajmg.a.30664. Am J Med Genet A. 2005. PMID: 15782410
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.
46 results