Keen-Kim D - Search Results

1

Quality Assurance of Non-Invasive Prenatal Screening (NIPS) for Fetal Aneuploidy Using Positive Predictive Values as Outcome Measures.

DiNonno W, Demko Z, Martin K, Billings P, Egbert M, Zneimer S, Keen-Kim D, Benn P. DiNonno W, et al. Among authors: keen kim d. J Clin Med. 2019 Aug 26;8(9):1311. doi: 10.3390/jcm8091311. J Clin Med. 2019. PMID: 31454954 Free PMC article.

2

Clinical experience with carrier screening in a general population: support for a comprehensive pan-ethnic approach.

Westemeyer M, Saucier J, Wallace J, Prins SA, Shetty A, Malhotra M, Demko ZP, Eng CM, Weckstein L, Boostanfar R, Rabinowitz M, Benn P, Keen-Kim D, Billings P. Westemeyer M, et al. Among authors: keen kim d. Genet Med. 2020 Aug;22(8):1320-1328. doi: 10.1038/s41436-020-0807-4. Epub 2020 May 5. Genet Med. 2020. PMID: 32366966 Free PMC article.

3

Correction: Clinical experience with carrier screening in a general population: support for a comprehensive pan-ethnic approach.

Westemeyer M, Saucier J, Wallace J, Prins SA, Shetty A, Malhotra M, Demko ZP, Eng CM, Weckstein L, Boostanfar R, Rabinowitz M, Benn P, Keen-Kim D, Billings P. Westemeyer M, et al. Among authors: keen kim d. Genet Med. 2020 Jul;22(7):1282. doi: 10.1038/s41436-020-0853-y. Genet Med. 2020. PMID: 32483296 Free PMC article.

4

Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses.

Keen-Kim D, Mathews CA, Reus VI, Lowe TL, Herrera LD, Budman CL, Gross-Tsur V, Pulver AE, Bruun RD, Erenberg G, Naarden A, Sabatti C, Freimer NB. Keen-Kim D, et al. Hum Mol Genet. 2006 Nov 15;15(22):3324-8. doi: 10.1093/hmg/ddl408. Epub 2006 Oct 11. Hum Mol Genet. 2006. PMID: 17035247

5

Genetics and epidemiology of Tourette syndrome.

Keen-Kim D, Freimer NB. Keen-Kim D, et al. J Child Neurol. 2006 Aug;21(8):665-71. doi: 10.1177/08830738060210081101. J Child Neurol. 2006. PMID: 16970867 Review.

6

Family-based genetic association study of DLGAP3 in Tourette Syndrome.

Crane J, Fagerness J, Osiecki L, Gunnell B, Stewart SE, Pauls DL, Scharf JM; Tourette Syndrome International Consortium for Genetics (TSAICG). Crane J, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):108-14. doi: 10.1002/ajmg.b.31134. Epub 2010 Nov 2. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21184590 Free PMC article.

7

Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample.

Scharf JM, Moorjani P, Fagerness J, Platko JV, Illmann C, Galloway B, Jenike E, Stewart SE, Pauls DL; Tourette Syndrome International Consortium for Genetics. Scharf JM, et al. Neurology. 2008 Apr 15;70(16 Pt 2):1495-6. doi: 10.1212/01.wnl.0000296833.25484.bb. Neurology. 2008. PMID: 18413575 Free PMC article. No abstract available.

8

Latent class analysis of gilles de la tourette syndrome using comorbidities: clinical and genetic implications.

Grados MA, Mathews CA; Tourette Syndrome Association International Consortium for Genetics. Grados MA, et al. Biol Psychiatry. 2008 Aug 1;64(3):219-25. doi: 10.1016/j.biopsych.2008.01.019. Epub 2008 Mar 21. Biol Psychiatry. 2008. PMID: 18359008 Free PMC article.

9

Assessment of an automated approach for variant interpretation in screening for monogenic disorders: A single-center study.

Gall BJ, Smart TB, Munch R, Kolluri S, Tadepally H, Lim KPH, Demko ZP, Benn P, Souter V, Sanapareddy N, Keen-Kim D. Gall BJ, et al. Among authors: keen kim d. Mol Genet Genomic Med. 2022 Dec;10(12):e2085. doi: 10.1002/mgg3.2085. Epub 2022 Nov 5. Mol Genet Genomic Med. 2022. PMID: 36333997 Free PMC article. Review.

10

KaryoTutor: an interactive cytogenetics training tool.

Keen-Kim D. Keen-Kim D. J Assoc Genet Technol. 2010;36(4):198-202. J Assoc Genet Technol. 2010. PMID: 21149991 No abstract available.

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