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Results by year

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

Year Number of Results
1881 2
1882 2
1884 1
1962 2
1963 4
1964 2
1965 2
1966 1
1967 6
1968 4
1969 6
1970 2
1971 6
1972 1
1973 2
1974 3
1975 5
1976 2
1977 3
1978 3
1979 3
1980 5
1981 1
1982 4
1983 2
1984 1
1985 2
1986 1
1987 4
1988 1
1989 2
1990 1
1991 1
1992 2
1994 2
1995 1
1996 2
1997 1
1998 2
1999 1
2000 2
2001 2
2003 1
2004 4
2005 2
2006 3
2008 2
2009 2
2010 3
2011 4
2014 2
2015 1
2016 3
2017 6
2018 2
2019 1
2020 6
2021 6
2022 3
2023 4
2024 0

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149 results

Results by year

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Page 1
HUWE1 variants cause dominant X-linked intellectual disability: a clinical study of 21 patients.
Moortgat S, Berland S, Aukrust I, Maystadt I, Baker L, Benoit V, Caro-Llopis A, Cooper NS, Debray FG, Faivre L, Gardeitchik T, Haukanes BI, Houge G, Kivuva E, Martinez F, Mehta SG, Nassogne MC, Powell-Hamilton N, Pfundt R, Rosello M, Prescott T, Vasudevan P, van Loon B, Verellen-Dumoulin C, Verloes A, Lippe CV, Wakeling E, Wilkie AOM, Wilson L, Yuen A, Study D, Low KJ, Newbury-Ecob RA. Moortgat S, et al. Among authors: lippe cv. Eur J Hum Genet. 2018 Jan;26(1):64-74. doi: 10.1038/s41431-017-0038-6. Epub 2017 Nov 27. Eur J Hum Genet. 2018. PMID: 29180823 Free PMC article.
Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability.
Cogné B, Ehresmann S, Beauregard-Lacroix E, Rousseau J, Besnard T, Garcia T, Petrovski S, Avni S, McWalter K, Blackburn PR, Sanders SJ, Uguen K, Harris J, Cohen JS, Blyth M, Lehman A, Berg J, Li MH, Kini U, Joss S, von der Lippe C, Gordon CT, Humberson JB, Robak L, Scott DA, Sutton VR, Skraban CM, Johnston JJ, Poduri A, Nordenskjöld M, Shashi V, Gerkes EH, Bongers EMHF, Gilissen C, Zarate YA, Kvarnung M, Lally KP, Kulch PA, Daniels B, Hernandez-Garcia A, Stong N, McGaughran J, Retterer K, Tveten K, Sullivan J, Geisheker MR, Stray-Pedersen A, Tarpinian JM, Klee EW, Sapp JC, Zyskind J, Holla ØL, Bedoukian E, Filippini F, Guimier A, Picard A, Busk ØL, Punetha J, Pfundt R, Lindstrand A, Nordgren A, Kalb F, Desai M, Ebanks AH, Jhangiani SN, Dewan T, Coban Akdemir ZH, Telegrafi A, Zackai EH, Begtrup A, Song X, Toutain A, Wentzensen IM, Odent S, Bonneau D, Latypova X, Deb W; CAUSES Study; Redon S, Bilan F, Legendre M, Troyer C, Whitlock K, Caluseriu O, Murphree MI, Pichurin PN, Agre K, Gavrilova R, Rinne T, Park M, Shain C, Heinzen EL, Xiao R, Amiel J, Lyonnet S, Isidor B, Biesecker LG, Lowenstein D, Posey JE, Denommé-Pichon AS; Deciphering Developmental Disorders study; Férec C, … See abstract for full author list ➔ Cogné B, et al. Among authors: von der lippe c. Am J Hum Genet. 2019 Mar 7;104(3):530-541. doi: 10.1016/j.ajhg.2019.01.010. Epub 2019 Feb 28. Am J Hum Genet. 2019. PMID: 30827496 Free PMC article.
[Gene panel testing].
Sørensen IW, Prescott T, F Rustad C, Blinkenberg EØ, Lippe CV. Sørensen IW, et al. Among authors: lippe cv. Tidsskr Nor Laegeforen. 2020 Feb 10;140(3). doi: 10.4045/tidsskr.19.0535. Print 2020 Feb 25. Tidsskr Nor Laegeforen. 2020. PMID: 32105034 Free article. Norwegian. No abstract available.
International Hiker with Acetazolamide Induced Glaucoma.
Tierney MG, Callahan CE, Lippe CM, Papachristou GC, Pujalte GG. Tierney MG, et al. Among authors: lippe cm. Curr Sports Med Rep. 2017 Mar/Apr;16(2):95-97. doi: 10.1249/JSR.0000000000000343. Curr Sports Med Rep. 2017. PMID: 28282355 No abstract available.
The impact of vasomotion on analysis of rodent fMRI data.
Lambers H, Wachsmuth L, Lippe C, Faber C. Lambers H, et al. Among authors: lippe c. Front Neurosci. 2023 Feb 24;17:1064000. doi: 10.3389/fnins.2023.1064000. eCollection 2023. Front Neurosci. 2023. PMID: 36908777 Free PMC article.
149 results