Ranola JMO - Search Results

1

Using Somatic Mutations from Tumors to Classify Variants in Mismatch Repair Genes.

Shirts BH, Konnick EQ, Upham S, Walsh T, Ranola JMO, Jacobson AL, King MC, Pearlman R, Hampel H, Pritchard CC. Shirts BH, et al. Among authors: ranola jmo. Am J Hum Genet. 2018 Jul 5;103(1):19-29. doi: 10.1016/j.ajhg.2018.05.001. Epub 2018 Jun 7. Am J Hum Genet. 2018. PMID: 29887214 Free PMC article.

2

Power of pedigree likelihood analysis in extended pedigrees to classify rare variants of uncertain significance in cancer risk genes.

Rosenthal EA, Ranola JMO, Shirts BH. Rosenthal EA, et al. Among authors: ranola jmo. Fam Cancer. 2017 Oct;16(4):611-620. doi: 10.1007/s10689-017-9989-6. Fam Cancer. 2017. PMID: 28534081 Free PMC article.

3

Outcomes of 92 patient-driven family studies for reclassification of variants of uncertain significance.

Tsai GJ, Rañola JMO, Smith C, Garrett LT, Bergquist T, Casadei S, Bowen DJ, Shirts BH. Tsai GJ, et al. Among authors: ranola jmo. Genet Med. 2019 Jun;21(6):1435-1442. doi: 10.1038/s41436-018-0335-7. Epub 2018 Oct 30. Genet Med. 2019. PMID: 30374176 Free article.

4

A comparison of cosegregation analysis methods for the clinical setting.

Rañola JMO, Liu Q, Rosenthal EA, Shirts BH. Rañola JMO, et al. Fam Cancer. 2018 Apr;17(2):295-302. doi: 10.1007/s10689-017-0017-7. Fam Cancer. 2018. PMID: 28695303 Free PMC article.

5

Modified capture-recapture estimates of the number of families with Lynch syndrome in Central Ohio.

Ranola JMO, Pearlman R, Hampel H, Shirts BH. Ranola JMO, et al. Fam Cancer. 2019 Jan;18(1):67-73. doi: 10.1007/s10689-018-0096-0. Fam Cancer. 2019. PMID: 30019097 Free PMC article.

6

An algorithm for optimal testing in co-segregation analysis.

Buie RW, Rañola JMO, Chen AT, Shirts BH. Buie RW, et al. Among authors: ranola jmo. Hum Mutat. 2022 May;43(5):547-556. doi: 10.1002/humu.24363. Epub 2022 Apr 7. Hum Mutat. 2022. PMID: 35225377 Free PMC article.

7

Exploring the effect of ascertainment bias on genetic studies that use clinical pedigrees.

Ranola JMO, Tsai GJ, Shirts BH. Ranola JMO, et al. Eur J Hum Genet. 2019 Dec;27(12):1800-1807. doi: 10.1038/s41431-019-0467-5. Epub 2019 Jul 11. Eur J Hum Genet. 2019. PMID: 31296927 Free PMC article.

8

Comparison of CDH1 Penetrance Estimates in Clinically Ascertained Families vs Families Ascertained for Multiple Gastric Cancers.

Roberts ME, Ranola JMO, Marshall ML, Susswein LR, Graceffo S, Bohnert K, Tsai G, Klein RT, Hruska KS, Shirts BH. Roberts ME, et al. Among authors: ranola jmo. JAMA Oncol. 2019 Sep 1;5(9):1325-1331. doi: 10.1001/jamaoncol.2019.1208. JAMA Oncol. 2019. PMID: 31246251 Free PMC article.

9

Estimating relationships between phenotypes and subjects drawn from admixed families.

Blue EM, Brown LA, Conomos MP, Kirk JL, Nato AQ Jr, Popejoy AB, Raffa J, Ranola J, Wijsman EM, Thornton T. Blue EM, et al. BMC Proc. 2016 Oct 18;10(Suppl 7):357-362. doi: 10.1186/s12919-016-0056-3. eCollection 2016. BMC Proc. 2016. PMID: 27980662 Free PMC article.

10

Convex clustering: an attractive alternative to hierarchical clustering.

Chen GK, Chi EC, Ranola JM, Lange K. Chen GK, et al. PLoS Comput Biol. 2015 May 12;11(5):e1004228. doi: 10.1371/journal.pcbi.1004228. eCollection 2015 May. PLoS Comput Biol. 2015. PMID: 25965340 Free PMC article.

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