Jessica Moline
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Explore the profile of Jessica Moline including associated specialties, affiliations and a list of published articles.
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22
Citations
603
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Recent Articles
1.
Xekouki P, Szarek E, Bullova P, Giubellino A, Quezado M, Mastroyannis S, et al.
J Clin Endocrinol Metab
. 2015 Feb;
100(5):E710-9.
PMID: 25695889
Context: Germline mutations in genes coding succinate dehydrogenase (SDH) subunits A, B, C, and D have been identified in familial paragangliomas (PGLs)/pheochromocytomas (PHEOs) and other tumors. We described a GH-secreting...
2.
3.
Pai R, Shadrach B, Carver P, Heald B, Moline J, Church J, et al.
Am J Surg Pathol
. 2014 Mar;
38(4):518-25.
PMID: 24625416
Differentiating sporadic microsatellite-unstable colorectal carcinoma due to MLH1 promoter hypermethylation from Lynch syndrome (LS)-associated tumors due to mutations in mismatch-repair proteins is time consuming, cost intensive, and requires advanced laboratory...
4.
Heald B, Gustafson S, Mester J, Arscott P, Lynch K, Moline J, et al.
J Natl Compr Canc Netw
. 2013 Sep;
11(9):1076-81.
PMID: 24029123
Analyses of time-based effort have determined that clinical genetic services are labor-intensive, although these data derive primarily from studying geneticists' efforts in the pediatric model. No studies have investigated the...
5.
Moline J, Mahdi H, Yang B, Biscotti C, Roma A, Heald B, et al.
Gynecol Oncol
. 2013 Apr;
130(1):121-6.
PMID: 23612316
Objectives: Lynch syndrome (LS) is a hereditary condition that increases the risk for endometrial and other cancers. Recognizing women at risk for LS based on personal/family history is burdensome and...
6.
Heald B, Plesec T, Liu X, Pai R, Patil D, Moline J, et al.
J Clin Oncol
. 2013 Feb;
31(10):1336-40.
PMID: 23401454
Purpose: In 2009, the Evaluation of Genomic Applications in Practice and Prevention recommended that all colorectal cancers (CRCs) be screened for Lynch syndrome (LS) through microsatellite instability (MSI) or immunohistochemistry...
7.
Ngeow J, Heald B, Rybicki L, Orloff M, Chen J, Liu X, et al.
Gastroenterology
. 2013 Feb;
144(7):1402-9, 1409.e1-5.
PMID: 23399955
Background & Aims: Gastrointestinal polyposis is a common clinical problem, yet there is no consensus on how to best manage patients with moderate-load polyposis. Identifying genetic features of this disorder...
8.
Moline J, Ngeow J, Rajiah P, Eng C
BMJ Case Rep
. 2012 Jun;
2011.
PMID: 22670000
A man in his 60s presents with chronic dyspnoea and cough for 3 years. EKG and nuclear stress test were not diagnostic. An echocardiogram revealed moderate pericardial effusion. His symptoms...
9.
Bishop J, Chae S, Patel S, Moline J, Ellingrod V
Psychiatry Res
. 2012 Apr;
199(1):74-6.
PMID: 22534499
We examined whether polymorphisms in the GRIK2, GRIA3 and GRIA1 genes were associated with selective serotonin reuptake inhibitor (SSRI)-associated sexual dysfunction in 114 participants treated for depression. One polymorphism in...
10.
Hobert J, Mester J, Moline J, Eng C
Genet Med
. 2012 Jan;
14(6):616-9.
PMID: 22261759
Purpose: Cowden syndrome results from germline mutations in the gene for phosphatase and tensin homologue deleted on chromosome 10 (PTEN) and from variants in succinate dehydrogenase B and D subunits....