Shuman C - Search Results

1

The Clinician-reported Genetic testing Utility InDEx (C-GUIDE): Preliminary evidence of validity and reliability.

Hayeems RZ, Luca S, Ungar WJ, Venkataramanan V, Tsiplova K, Bashir NS, Costain G, Inglese C, McNiven V, Quercia N, Shugar A, Yoon G, Cytrynbaum C, Dupuis L, Shao Z, Hewson S, Shuman C, Aul R, Liston E, Babul-Hirji R, Bushby A, Pullenayegum E, Chad L, Meyn MS. Hayeems RZ, et al. Among authors: shuman c. Genet Med. 2022 Feb;24(2):430-438. doi: 10.1016/j.gim.2021.10.005. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906486 Free article.

2

Attitudes regarding predictive testing for retinitis pigmentosa.

Mezer E, Babul-Hirji R, Wise R, Chipman M, DaSilva L, Rowell M, Thackray R, Shuman CT, Levin AV. Mezer E, et al. Ophthalmic Genet. 2007 Mar;28(1):9-15. doi: 10.1080/13816810701199423. Ophthalmic Genet. 2007. PMID: 17454742

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

Personality traits associated with genetic counselor compassion fatigue: the roles of dispositional optimism and locus of control.

Injeyan MC, Shuman C, Shugar A, Chitayat D, Atenafu EG, Kaiser A. Injeyan MC, et al. Among authors: shuman c. J Genet Couns. 2011 Oct;20(5):526-40. doi: 10.1007/s10897-011-9379-4. Epub 2011 Jun 24. J Genet Couns. 2011. PMID: 21701957

5

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

6

22q11.2 deletion syndrome: attitudes towards disclosing the risk of psychiatric illness.

Martin N, Mikhaelian M, Cytrynbaum C, Shuman C, Chitayat DA, Weksberg R, Bassett AS. Martin N, et al. Among authors: shuman c. J Genet Couns. 2012 Dec;21(6):825-34. doi: 10.1007/s10897-012-9517-7. Epub 2012 Jul 26. J Genet Couns. 2012. PMID: 22833231 Free PMC article.

7

Mosaicism for genome-wide paternal uniparental disomy with features of multiple imprinting disorders: diagnostic and management issues.

Inbar-Feigenberg M, Choufani S, Cytrynbaum C, Chen YA, Steele L, Shuman C, Ray PN, Weksberg R. Inbar-Feigenberg M, et al. Among authors: shuman c. Am J Med Genet A. 2013 Jan;161A(1):13-20. doi: 10.1002/ajmg.a.35651. Epub 2012 Dec 13. Am J Med Genet A. 2013. PMID: 23239666

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

Counseling and screening for cystic fibrosis in patients with congenital bilateral absence of the vas deferens: Patient perceptions.

Fitzpatrick JL, Hutton EM, Babul R, Cytrynbaum CS, Sutherland JE, Shuman CT. Fitzpatrick JL, et al. Among authors: shuman ct. J Genet Couns. 1996 Mar;5(1):1-15. doi: 10.1007/BF01408661. J Genet Couns. 1996. PMID: 24234558

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

246 results

Search Page