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Cyclic vomiting syndrome and mitochondrial DNA mutations.

Boles RG, Chun N, Senadheera D, Wong LJ. Boles RG, et al. Among authors: chun n. Lancet. 1997 Nov 1;350(9087):1299-300. doi: 10.1016/S0140-6736(05)62477-4. Lancet. 1997. PMID: 9357417 No abstract available.

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Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locus.

Pulleyn LJ, Reardon W, Wilkes D, Rutland P, Jones BM, Hayward R, Hall CM, Brueton L, Chun N, Lammer E, Malcolm S, Winter RM. Pulleyn LJ, et al. Among authors: chun n. Eur J Hum Genet. 1996;4(5):283-91. doi: 10.1159/000472215. Eur J Hum Genet. 1996. PMID: 8946174

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The MLH1 c.-27C>A and c.85G>T variants are linked to dominantly inherited MLH1 epimutation and are borne on a European ancestral haplotype.

Kwok CT, Vogelaar IP, van Zelst-Stams WA, Mensenkamp AR, Ligtenberg MJ, Rapkins RW, Ward RL, Chun N, Ford JM, Ladabaum U, McKinnon WC, Greenblatt MS, Hitchins MP. Kwok CT, et al. Among authors: chun n. Eur J Hum Genet. 2014 May;22(5):617-24. doi: 10.1038/ejhg.2013.200. Epub 2013 Oct 2. Eur J Hum Genet. 2014. PMID: 24084575 Free PMC article.

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Identification of an intronic single nucleotide polymorphism leading to allele dropout during validation of a CDH1 sequencing assay: implications for designing polymerase chain reaction-based assays.

Mullins FM, Dietz L, Lay M, Zehnder JL, Ford J, Chun N, Schrijver I. Mullins FM, et al. Among authors: chun n. Genet Med. 2007 Nov;9(11):752-60. doi: 10.1097/gim.0b013e318159a369. Genet Med. 2007. PMID: 18007144

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Identification of a novel p53 in-frame deletion in a Li-Fraumeni-like family.

Schiffman JD, Chun N, Fisher PG, Dahl GV, Ford JM, Eggerding FA. Schiffman JD, et al. Among authors: chun n. Pediatr Blood Cancer. 2008 Apr;50(4):914-6. doi: 10.1002/pbc.21247. Pediatr Blood Cancer. 2008. PMID: 17554785

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Parent decision-making around the genetic testing of children for germline TP53 mutations.

Alderfer MA, Zelley K, Lindell RB, Novokmet A, Mai PL, Garber JE, Nathan D, Scollon S, Chun NM, Patenaude AF, Ford JM, Plon SE, Schiffman JD, Diller LR, Savage SA, Malkin D, Ford CA, Nichols KE. Alderfer MA, et al. Cancer. 2015 Jan 15;121(2):286-93. doi: 10.1002/cncr.29027. Epub 2014 Sep 15. Cancer. 2015. PMID: 25223899

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Hereditary diffuse gastric cancer due to a previously undescribed CDH1 splice site mutation.

Matsukuma KE, Mullins FM, Dietz L, Zehnder JL, Ford JM, Chun NM, Schrijver I. Matsukuma KE, et al. Hum Pathol. 2010 Aug;41(8):1200-3. doi: 10.1016/j.humpath.2010.01.022. Hum Pathol. 2010. PMID: 20624523

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Racial/ethnic differences in multiple-gene sequencing results for hereditary cancer risk.

Caswell-Jin JL, Gupta T, Hall E, Petrovchich IM, Mills MA, Kingham KE, Koff R, Chun NM, Levonian P, Lebensohn AP, Ford JM, Kurian AW. Caswell-Jin JL, et al. Genet Med. 2018 Feb;20(2):234-239. doi: 10.1038/gim.2017.96. Epub 2017 Jul 27. Genet Med. 2018. PMID: 28749474

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Performance of BRCA1/2 mutation prediction models in Asian Americans.

Kurian AW, Gong GD, Chun NM, Mills MA, Staton AD, Kingham KE, Crawford BB, Lee R, Chan S, Donlon SS, Ridge Y, Panabaker K, West DW, Whittemore AS, Ford JM. Kurian AW, et al. J Clin Oncol. 2008 Oct 10;26(29):4752-8. doi: 10.1200/JCO.2008.16.8310. Epub 2008 Sep 8. J Clin Oncol. 2008. PMID: 18779604 Free PMC article.

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Patient communication of cancer genetic test results in a diverse population.

Ricker CN, Koff RB, Qu C, Culver J, Sturgeon D, Kingham KE, Lowstuter K, Chun NM, Rowe-Teeter C, Lebensohn A, Levonian P, Partynski K, Lara-Otero K, Hong C, Petrovchich IM, Mills MA, Hartman AR, Allen B, Ladabaum U, McDonnell K, Ford JM, Gruber SB, Kurian AW, Idos GE. Ricker CN, et al. Among authors: chun nm. Transl Behav Med. 2018 Jan 29;8(1):85-94. doi: 10.1093/tbm/ibx010. Transl Behav Med. 2018. PMID: 29385580 Free PMC article.

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