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

Year Number of Results
1978 1
1979 5
1981 3
1982 1
1983 4
1984 1
1985 3
1986 4
1987 4
1988 4
1989 4
1990 5
1991 1
1992 3
1993 4
1994 5
1995 5
1996 3
1997 4
1998 5
1999 2
2000 2
2001 3
2002 2
2003 2
2004 3
2005 5
2006 2
2009 2
2010 2
2011 1
2012 1
2014 1
2015 4
2016 3
2019 1
2020 1
2021 1
2022 1
2023 3
2024 1
2025 0

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109 results

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Page 1
Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
Amendola LM, Dorschner MO, Robertson PD, Salama JS, Hart R, Shirts BH, Murray ML, Tokita MJ, Gallego CJ, Kim DS, Bennett JT, Crosslin DR, Ranchalis J, Jones KL, Rosenthal EA, Jarvik ER, Itsara A, Turner EH, Herman DS, Schleit J, Burt A, Jamal SM, Abrudan JL, Johnson AD, Conlin LK, Dulik MC, Santani A, Metterville DR, Kelly M, Foreman AK, Lee K, Taylor KD, Guo X, Crooks K, Kiedrowski LA, Raffel LJ, Gordon O, Machini K, Desnick RJ, Biesecker LG, Lubitz SA, Mulchandani S, Cooper GM, Joffe S, Richards CS, Yang Y, Rotter JI, Rich SS, O'Donnell CJ, Berg JS, Spinner NB, Evans JP, Fullerton SM, Leppig KA, Bennett RL, Bird T, Sybert VP, Grady WM, Tabor HK, Kim JH, Bamshad MJ, Wilfond B, Motulsky AG, Scott CR, Pritchard CC, Walsh TD, Burke W, Raskind WH, Byers P, Hisama FM, Rehm H, Nickerson DA, Jarvik GP. Amendola LM, et al. Among authors: sybert vp. Genome Res. 2015 Mar;25(3):305-15. doi: 10.1101/gr.183483.114. Epub 2015 Jan 30. Genome Res. 2015. PMID: 25637381 Free PMC article.
Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.
Wright JT, Fete M, Schneider H, Zinser M, Koster MI, Clarke AJ, Hadj-Rabia S, Tadini G, Pagnan N, Visinoni AF, Bergendal B, Abbott B, Fete T, Stanford C, Butcher C, D'Souza RN, Sybert VP, Morasso MI. Wright JT, et al. Among authors: sybert vp. Am J Med Genet A. 2019 Mar;179(3):442-447. doi: 10.1002/ajmg.a.61045. Epub 2019 Jan 31. Am J Med Genet A. 2019. PMID: 30703280 Free PMC article. Review.
Turner's syndrome.
Sybert VP, McCauley E. Sybert VP, et al. N Engl J Med. 2004 Sep 16;351(12):1227-38. doi: 10.1056/NEJMra030360. N Engl J Med. 2004. PMID: 15371580 Review. No abstract available.
Incontinentia pigmenti.
Francis JS, Sybert VP. Francis JS, et al. Among authors: sybert vp. Semin Cutan Med Surg. 1997 Mar;16(1):54-60. doi: 10.1016/s1085-5629(97)80036-3. Semin Cutan Med Surg. 1997. PMID: 9125766 Review.
Mosaicism in cutaneous pigmentation.
Lombillo VA, Sybert VP. Lombillo VA, et al. Among authors: sybert vp. Curr Opin Pediatr. 2005 Aug;17(4):494-500. doi: 10.1097/01.mop.0000171319.84053.45. Curr Opin Pediatr. 2005. PMID: 16012262 Review.
Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts.
Blue EE, Huang SJ, Khan A, Golden-Grant K, Boyd B, Rosenthal EA, Gillentine MA, Fleming LR, Adams DR, Wolfe L, Allworth A, Bamshad MJ, Caruana NJ, Chanprasert S, Chen J, Dargie N, Doherty D, Friederich MW, Hisama FM, Horike-Pyne M, Lee JC, Donovan TE, Hock DH, Leppig KA, Miller DE, Mirzaa G, Ranchalis J, Raskind WH, Michel CR, Reisdorph R, Schwarze U, Sheppeard S, Strohbehn S, Stroud DA, Sybert VP, Wener MH; University of Washington Center for Rare Disease Research, the Undiagnosed Diseases Network; Stergachis AB, Lam CT, Jarvik GP, Dipple KM, Van Hove JLK, Glass IA. Blue EE, et al. Among authors: sybert vp. Rare. 2024;2:100040. doi: 10.1016/j.rare.2024.100040. Epub 2024 Aug 14. Rare. 2024. PMID: 39421685 Free PMC article.
Rapp-Hodgkin ectodermal dysplasia.
Schroeder HW Jr, Sybert VP. Schroeder HW Jr, et al. Among authors: sybert vp. J Pediatr. 1987 Jan;110(1):72-5. doi: 10.1016/s0022-3476(87)80291-3. J Pediatr. 1987. PMID: 3794888
Understanding aneuploidy.
Siegel DH, Sybert VP. Siegel DH, et al. Among authors: sybert vp. Pediatr Dermatol. 2005 May-Jun;22(3):270-5. doi: 10.1111/j.1525-1470.2005.22323.x. Pediatr Dermatol. 2005. PMID: 15916583 Review. No abstract available.
109 results