Dianne Keen-Kim - Search Results

Year	Number of Results
2005	1
2006	3
2008	1
2010	1
2019	1
2020	2
2022	1
2024	0

1

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.

2

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.

3

Cytogenetic biomarkers for human cancer.

Keen-Kim D, Nooraie F, Rao PN. Keen-Kim D, et al. Front Biosci. 2008 May 1;13:5928-49. doi: 10.2741/3127. Front Biosci. 2008. PMID: 18508633 Review.

4

Microelectronic array system for molecular diagnostic genotyping: Nanogen NanoChip 400 and molecular biology workstation.

Keen-Kim D, Grody WW, Richards CS. Keen-Kim D, et al. Expert Rev Mol Diagn. 2006 May;6(3):287-94. doi: 10.1586/14737159.6.3.287. Expert Rev Mol Diagn. 2006. PMID: 16706733 Review.

5

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.

6

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.

7

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.

8

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

9

Validation and clinical application of a locus-specific polymerase chain reaction- and minisequencing-based assay for congenital adrenal hyperplasia (21-hydroxylase deficiency).

Keen-Kim D, Redman JB, Alanes RU, Eachus MM, Wilson RC, New MI, Nakamoto JM, Fenwick RG. Keen-Kim D, et al. J Mol Diagn. 2005 May;7(2):236-46. doi: 10.1016/S1525-1578(10)60550-8. J Mol Diagn. 2005. PMID: 15858147 Free PMC article.

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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