Shuman C - Search Results

1

Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray.

Hayeems RZ, Bhawra J, Tsiplova K, Meyn MS, Monfared N, Bowdin S, Stavropoulos DJ, Marshall CR, Basran R, Shuman C, Ito S, Cohn I, Hum C, Girdea M, Brudno M, Cohn RD, Scherer SW, Ungar WJ. Hayeems RZ, et al. Among authors: shuman c. Eur J Hum Genet. 2017 Dec;25(12):1303-1312. doi: 10.1038/s41431-017-0020-3. Epub 2017 Nov 20. Eur J Hum Genet. 2017. PMID: 29158552 Free PMC article.

2

Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome.

Nakabayashi K, Fernandez BA, Teshima I, Shuman C, Proud VK, Curry CJ, Chitayat D, Grebe T, Ming J, Oshimura M, Meguro M, Mitsuya K, Deb-Rinker P, Herbrick JA, Weksberg R, Scherer SW. Nakabayashi K, et al. Among authors: shuman c. Genomics. 2002 Feb;79(2):186-96. doi: 10.1006/geno.2002.6695. Genomics. 2002. PMID: 11829489

3

The cycle of genome-directed medicine.

Buchanan JA, Carson AR, Chitayat D, Malkin D, Meyn MS, Ray PN, Shuman C, Weksberg R, Scherer SW. Buchanan JA, et al. Among authors: shuman c. Genome Med. 2009 Feb 2;1(2):16. doi: 10.1186/gm16. Genome Med. 2009. PMID: 19341487 Free PMC article.

4

Whole genome scanning: resolving clinical diagnosis and management amidst complex data.

Ali-Khan SE, Daar AS, Shuman C, Ray PN, Scherer SW. Ali-Khan SE, et al. Among authors: shuman c. Pediatr Res. 2009 Oct;66(4):357-63. doi: 10.1203/PDR.0b013e3181b0cbd8. Pediatr Res. 2009. PMID: 19531980 Review.

5

Beckwith-Wiedemann syndrome.

Weksberg R, Shuman C, Beckwith JB. Weksberg R, et al. Among authors: shuman c. Eur J Hum Genet. 2010 Jan;18(1):8-14. doi: 10.1038/ejhg.2009.106. Eur J Hum Genet. 2010. PMID: 19550435 Free PMC article. Review.

6

Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell-Silver syndrome.

Horike S, Ferreira JC, Meguro-Horike M, Choufani S, Smith AC, Shuman C, Meschino W, Chitayat D, Zackai E, Scherer SW, Weksberg R. Horike S, et al. Among authors: shuman c. Am J Med Genet A. 2009 Nov;149A(11):2415-23. doi: 10.1002/ajmg.a.33065. Am J Med Genet A. 2009. PMID: 19876907

7

Parents' perspectives on participating in genetic research in autism.

Trottier M, Roberts W, Drmic I, Scherer SW, Weksberg R, Cytrynbaum C, Chitayat D, Shuman C, Miller FA. Trottier M, et al. Among authors: shuman c. J Autism Dev Disord. 2013 Mar;43(3):556-68. doi: 10.1007/s10803-012-1592-y. J Autism Dev Disord. 2013. PMID: 22782649

8

Risk estimates for complex disorders: comparing personal genome testing and family history.

Aiyar L, Shuman C, Hayeems R, Dupuis A, Pu S, Wodak S, Chitayat D, Velsher L, Davies J. Aiyar L, et al. Among authors: shuman c. Genet Med. 2014 Mar;16(3):231-7. doi: 10.1038/gim.2013.115. Epub 2013 Sep 5. Genet Med. 2014. PMID: 24009002 Free article.

9

High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith-Wiedemann syndrome.

Baskin B, Choufani S, Chen YA, Shuman C, Parkinson N, Lemyre E, Micheil Innes A, Stavropoulos DJ, Ray PN, Weksberg R. Baskin B, et al. Among authors: shuman c. Hum Genet. 2014 Mar;133(3):321-30. doi: 10.1007/s00439-013-1379-z. Epub 2013 Oct 24. Hum Genet. 2014. PMID: 24154661

10

Predictive genomic testing of children for adult onset disorders: a Canadian perspective.

Szego MJ, Meyn MS, Anderson JA, Hayeems R, Shuman C, Monfared N, Bowdin S, Shaul RZ. Szego MJ, et al. Among authors: shuman c. Am J Bioeth. 2014;14(3):19-21. doi: 10.1080/15265161.2013.879960. Am J Bioeth. 2014. PMID: 24592833 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

252 results

Search Page

Filters