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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2013 2
2014 4
2015 7
2016 4
2017 5
2018 16
2019 6
2020 3
2021 10
2022 3
2023 4
2024 0

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48 results

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Page 1
Interpreting secondary cardiac disease variants in an exome cohort.
Ng D, Johnston JJ, Teer JK, Singh LN, Peller LC, Wynter JS, Lewis KL, Cooper DN, Stenson PD, Mullikin JC, Biesecker LG; NIH Intramural Sequencing Center (NISC) Comparative Sequencing Program. Ng D, et al. Among authors: lewis kl. Circ Cardiovasc Genet. 2013 Aug;6(4):337-46. doi: 10.1161/CIRCGENETICS.113.000039. Epub 2013 Jul 16. Circ Cardiovasc Genet. 2013. PMID: 23861362 Free PMC article.
Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number.
Lyons JJ, Yu X, Hughes JD, Le QT, Jamil A, Bai Y, Ho N, Zhao M, Liu Y, O'Connell MP, Trivedi NN, Nelson C, DiMaggio T, Jones N, Matthews H, Lewis KL, Oler AJ, Carlson RJ, Arkwright PD, Hong C, Agama S, Wilson TM, Tucker S, Zhang Y, McElwee JJ, Pao M, Glover SC, Rothenberg ME, Hohman RJ, Stone KD, Caughey GH, Heller T, Metcalfe DD, Biesecker LG, Schwartz LB, Milner JD. Lyons JJ, et al. Among authors: lewis kl. Nat Genet. 2016 Dec;48(12):1564-1569. doi: 10.1038/ng.3696. Epub 2016 Oct 17. Nat Genet. 2016. PMID: 27749843 Free PMC article.
Common genetic susceptibility loci link PFAPA syndrome, Behçet's disease, and recurrent aphthous stomatitis.
Manthiram K, Preite S, Dedeoglu F, Demir S, Ozen S, Edwards KM, Lapidus S, Katz AE; Genomic Ascertainment Cohort; Feder HM Jr, Lawton M, Licameli GR, Wright PF, Le J, Barron KS, Ombrello AK, Barham B, Romeo T, Jones A, Srinivasalu H, Mudd PA, DeBiasi RL, Gül A, Marshall GS, Jones OY, Chandrasekharappa SC, Stepanovskiy Y, Ferguson PJ, Schwartzberg PL, Remmers EF, Kastner DL. Manthiram K, et al. Proc Natl Acad Sci U S A. 2020 Jun 23;117(25):14405-14411. doi: 10.1073/pnas.2002051117. Epub 2020 Jun 9. Proc Natl Acad Sci U S A. 2020. PMID: 32518111 Free PMC article.
Ethnic identity and engagement with genome sequencing research.
Turbitt E, Roberts MC, Hollister BM, Lewis KL, Biesecker LG, Klein WMP. Turbitt E, et al. Among authors: lewis kl. Genet Med. 2019 Aug;21(8):1735-1743. doi: 10.1038/s41436-018-0410-0. Epub 2018 Dec 20. Genet Med. 2019. PMID: 30568309 Free PMC article.
The Dynamics of a Genetic Counseling Peer Supervision Group.
Lewis KL, Erby LAH, Bergner AL, Reed EK, Johnson MR, Adcock JY, Weaver MA. Lewis KL, et al. J Genet Couns. 2017 Jun;26(3):532-540. doi: 10.1007/s10897-016-0013-3. Epub 2016 Sep 13. J Genet Couns. 2017. PMID: 27618824
Increased Burden of Rare Sequence Variants in GnRH-Associated Genes in Women With Hypothalamic Amenorrhea.
Delaney A, Burkholder AB, Lavender CA, Plummer L, Mericq V, Merino PM, Quinton R, Lewis KL, Meader BN, Albano A, Shaw ND, Welt CK, Martin KA, Seminara SB, Biesecker LG, Bailey-Wilson JE, Hall JE. Delaney A, et al. Among authors: lewis kl. J Clin Endocrinol Metab. 2021 Mar 8;106(3):e1441-e1452. doi: 10.1210/clinem/dgaa609. J Clin Endocrinol Metab. 2021. PMID: 32870266 Free PMC article.
48 results