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

Year Number of Results
1965 3
1966 1
1967 6
1968 4
1970 1
1971 4
1972 5
1973 3
1974 3
1975 3
1976 3
1977 4
1978 2
1979 2
1981 2
1988 1
2009 2
2010 1
2012 2
2013 4
2014 3
2017 2
2019 2
2020 3
2021 3
2022 2
2024 0

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66 results

Results by year

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Page 1
Biallelic PI4KA variants cause neurological, intestinal and immunological disease.
Salter CG, Cai Y, Lo B, Helman G, Taylor H, McCartney A, Leslie JS, Accogli A, Zara F, Traverso M, Fasham J, Lees JA, Ferla MP, Chioza BA, Wenger O, Scott E, Cross HE, Crawford J, Warshawsky I, Keisling M, Agamanolis D, Ward Melver C, Cox H, Elawad M, Marton T, Wakeling MN, Holzinger D, Tippelt S, Munteanu M, Valcheva D, Deal C, Van Meerbeke S, Walsh Vockley C, Butte MJ, Acar U, van der Knaap MS, Korenke GC, Kotzaeridou U, Balla T, Simons C, Uhlig HH, Crosby AH, De Camilli P, Wolf NI, Baple EL. Salter CG, et al. Among authors: cross he. Brain. 2021 Dec 31;144(12):3597-3610. doi: 10.1093/brain/awab313. Brain. 2021. PMID: 34415310 Free PMC article.
Familial nanophthalmos.
Cross HE, Yoder F. Cross HE, et al. Am J Ophthalmol. 1976 Mar;81(3):300-6. doi: 10.1016/0002-9394(76)90244-0. Am J Ophthalmol. 1976. PMID: 1258954
Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalities.
Leslie JS, Hjeij R, Vivante A, Bearce EA, Dyer L, Wang J, Rawlins L, Kennedy J, Ubeyratna N, Fasham J, Irons ZH, Craig SB, Koenig J, George S, Pode-Shakked B, Bolkier Y, Barel O, Mane S, Frederiksen KK, Wenger O, Scott E, Cross HE, Lorentzen E, Norris DP, Anikster Y, Omran H, Grimes DT, Crosby AH, Baple EL. Leslie JS, et al. Among authors: cross he. Genet Med. 2022 Nov;24(11):2249-2261. doi: 10.1016/j.gim.2022.07.019. Epub 2022 Sep 8. Genet Med. 2022. PMID: 36074124 Free PMC article.
Amish demography.
Cross HE, McKusick VA. Cross HE, et al. Soc Biol. 1970 Jun;17(2):83-101. doi: 10.1080/19485565.1970.9987850. Soc Biol. 1970. PMID: 5538247 No abstract available.
Functional roles of bestrophins in ocular epithelia.
Marmorstein AD, Cross HE, Peachey NS. Marmorstein AD, et al. Among authors: cross he. Prog Retin Eye Res. 2009 May;28(3):206-26. doi: 10.1016/j.preteyeres.2009.04.004. Epub 2009 May 4. Prog Retin Eye Res. 2009. PMID: 19398034 Free PMC article. Review.
The Rieger syndrome.
Jorgenson RJ, Levin LS, Cross HE, Yoder F, Kelly TE. Jorgenson RJ, et al. Among authors: cross he. Am J Med Genet. 1978;2(3):307-18. doi: 10.1002/ajmg.1320020310. Am J Med Genet. 1978. PMID: 263445
Type II syndactyly.
Cross HE, Lerberg DB, McKusick VA. Cross HE, et al. Am J Hum Genet. 1968 Jul;20(4):368-80. Am J Hum Genet. 1968. PMID: 4298538 Free PMC article. No abstract available.
Arcuate corneal opacities.
Smith JW, Smalley LA, Cross HE. Smith JW, et al. Among authors: cross he. Am J Med Sci. 1977 Mar-Apr;273(2):197-201. doi: 10.1097/00000441-197703000-00010. Am J Med Sci. 1977. PMID: 860734 No abstract available.
No association between SCN9A and monogenic human epilepsy disorders.
Fasham J, Leslie JS, Harrison JW, Deline J, Williams KB, Kuhl A, Scott Schwoerer J, Cross HE, Crosby AH, Baple EL. Fasham J, et al. Among authors: cross he. PLoS Genet. 2020 Nov 20;16(11):e1009161. doi: 10.1371/journal.pgen.1009161. eCollection 2020 Nov. PLoS Genet. 2020. PMID: 33216760 Free PMC article.
66 results