Sherman SL - Search Results

1

Descriptive analysis of seizures and comorbidities associated with fragile X syndrome.

Albizua I, Charen K, Shubeck L, Talboy A, Berry-Kravis E, Kaufmann WE, Stallworth JL, Drazba KT, Erickson CA, Sweeney JA, Tartaglia N, Warren SF, Hagerman R, Sherman SL, Warren ST, Jin P, Allen EG. Albizua I, et al. Among authors: sherman sl. Mol Genet Genomic Med. 2022 Aug;10(8):e2001. doi: 10.1002/mgg3.2001. Epub 2022 Jul 18. Mol Genet Genomic Med. 2022. PMID: 35852003 Free PMC article.

2

Human genes containing polymorphic trinucleotide repeats.

Riggins GJ, Lokey LK, Chastain JL, Leiner HA, Sherman SL, Wilkinson KD, Warren ST. Riggins GJ, et al. Among authors: sherman sl. Nat Genet. 1992 Nov;2(3):186-91. doi: 10.1038/ng1192-186. Nat Genet. 1992. PMID: 1345166

3

Collaborative prospective study of the fragile X syndrome: one-year progress report.

Sherman SL, Barbi G, Brøndum-Nielsen K, Brown WT, Carpenter NJ, Chudley AE, Ferraz OP, Ferreira P, Gustavson KH, Halliday J, et al. Sherman SL, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):355-60. doi: 10.1002/ajmg.1320430155. Am J Med Genet. 1992. PMID: 1605212

4

Collaborative prospective study of the fragile X syndrome: request for participation.

Sherman SL. Sherman SL. Am J Med Genet. 1991 Feb-Mar;38(2-3):396-9. doi: 10.1002/ajmg.1320380248. Am J Med Genet. 1991. PMID: 2018079

5

CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosome.

Riggins GJ, Sherman SL, Phillips CN, Stock W, Westbrook CA, Warren ST. Riggins GJ, et al. Among authors: sherman sl. Genes Chromosomes Cancer. 1994 Feb;9(2):141-4. doi: 10.1002/gcc.2870090211. Genes Chromosomes Cancer. 1994. PMID: 7513545

6

Normal variation at the myotonic dystrophy locus in global human populations.

Zerylnick C, Torroni A, Sherman SL, Warren ST. Zerylnick C, et al. Among authors: sherman sl. Am J Hum Genet. 1995 Jan;56(1):123-30. Am J Hum Genet. 1995. PMID: 7825567 Free PMC article.

7

Seventh International Workshop on the Fragile X and X-linked Mental Retardation.

Tranebjaerg L, Lubs HA, Borghgraef M, Brown WT, Fisch G, Fryns JP, Hagerman R, Jacobs PA, Mandel JL, Mulley J, Oostra B, Schwartz C, Sherman S, Willard H, Willems P. Tranebjaerg L, et al. Am J Med Genet. 1996 Jul 12;64(1):1-14. doi: 10.1002/(SICI)1096-8628(19960712)64:1<1::AID-AJMG1>3.0.CO;2-Z. Am J Med Genet. 1996. PMID: 8826442 No abstract available.

8

Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population.

Meadows KL, Pettay D, Newman J, Hersey J, Ashley AE, Sherman SL. Meadows KL, et al. Among authors: sherman sl. Am J Med Genet. 1996 Aug 9;64(2):428-33. doi: 10.1002/(SICI)1096-8628(19960809)64:2<428::AID-AJMG39>3.0.CO;2-F. Am J Med Genet. 1996. PMID: 8844098

9

Examination of factors associated with instability of the FMR1 CGG repeat.

Ashley-Koch AE, Robinson H, Glicksman AE, Nolin SL, Schwartz CE, Brown WT, Turner G, Sherman SL. Ashley-Koch AE, et al. Among authors: sherman sl. Am J Hum Genet. 1998 Sep;63(3):776-85. doi: 10.1086/302018. Am J Hum Genet. 1998. PMID: 9718348 Free PMC article.

10

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.

Gunter C, Paradee W, Crawford DC, Meadows KA, Newman J, Kunst CB, Nelson DL, Schwartz C, Murray A, Macpherson JN, Sherman SL, Warren ST. Gunter C, et al. Among authors: sherman sl. Hum Mol Genet. 1998 Nov;7(12):1935-46. doi: 10.1093/hmg/7.12.1935. Hum Mol Genet. 1998. PMID: 9811938

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