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Results by year

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

Year Number of Results
1933 4
1939 2
1948 3
1951 1
1952 2
1953 6
1954 2
1955 2
1956 3
1957 2
1958 2
1959 1
1960 1
1961 1
1962 2
1963 1
1966 1
1967 1
1968 2
1969 1
1970 2
1977 1
1981 1
1984 2
1985 3
1987 4
1988 2
1991 2
1992 2
1993 4
1994 2
1996 3
1997 1
1998 6
1999 4
2000 4
2001 3
2002 3
2003 10
2004 10
2005 10
2006 7
2007 20
2008 13
2009 10
2010 5
2011 9
2012 16
2013 19
2014 28
2015 28
2016 30
2017 37
2018 34
2019 51
2020 52
2021 47
2022 50
2023 30

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Article type

Publication date

Search Results

543 results

Results by year

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Page 1
Refractive errors.
Schiefer U, Kraus C, Baumbach P, Ungewiß J, Michels R. Schiefer U, et al. Among authors: kraus c. Dtsch Arztebl Int. 2016 Oct 14;113(41):693-702. doi: 10.3238/arztebl.2016.0693. Dtsch Arztebl Int. 2016. PMID: 27839543 Free PMC article. Review.
[Shaken baby syndrome].
Reith W, Yilmaz U, Kraus C. Reith W, et al. Among authors: kraus c. Radiologe. 2016 May;56(5):424-31. doi: 10.1007/s00117-016-0106-x. Radiologe. 2016. PMID: 27118366 Review. German.
Vulvar Lichen Sclerosus.
Kraus CN. Kraus CN. JAMA Dermatol. 2022 Sep 1;158(9):1088. doi: 10.1001/jamadermatol.2022.0359. JAMA Dermatol. 2022. PMID: 35793083 No abstract available.
CRISPR/Cas9-mediated excision of ALS/FTD-causing hexanucleotide repeat expansion in C9ORF72 rescues major disease mechanisms in vivo and in vitro.
Meijboom KE, Abdallah A, Fordham NP, Nagase H, Rodriguez T, Kraus C, Gendron TF, Krishnan G, Esanov R, Andrade NS, Rybin MJ, Ramic M, Stephens ZD, Edraki A, Blackwood MT, Kahriman A, Henninger N, Kocher JA, Benatar M, Brodsky MH, Petrucelli L, Gao FB, Sontheimer EJ, Brown RH, Zeier Z, Mueller C. Meijboom KE, et al. Among authors: kraus c. Nat Commun. 2022 Oct 21;13(1):6286. doi: 10.1038/s41467-022-33332-7. Nat Commun. 2022. PMID: 36271076 Free PMC article.
Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior.
Harris HK, Nakayama T, Lai J, Zhao B, Argyrou N, Gubbels CS, Soucy A, Genetti CA, Suslovitch V, Rodan LH, Tiller GE, Lesca G, Gripp KW, Asadollahi R, Hamosh A, Applegate CD, Turnpenny PD, Simon MEH, Volker-Touw CML, Gassen KLIV, Binsbergen EV, Pfundt R, Gardeitchik T, Vries BBA, Immken LL, Buchanan C, Willing M, Toler TL, Fassi E, Baker L, Vansenne F, Wang X, Ambrus JL Jr, Fannemel M, Posey JE, Agolini E, Novelli A, Rauch A, Boonsawat P, Fagerberg CR, Larsen MJ, Kibaek M, Labalme A, Poisson A, Payne KK, Walsh LE, Aldinger KA, Balciuniene J, Skraban C, Gray C, Murrell J, Bupp CP, Pascolini G, Grammatico P, Broly M, Küry S, Nizon M, Rasool IG, Zahoor MY, Kraus C, Reis A, Iqbal M, Uguen K, Audebert-Bellanger S, Ferec C, Redon S, Baker J, Wu Y, Zampino G, Syrbe S, Brosse I, Jamra RA, Dobyns WB, Cohen LL, Blomhoff A, Mignot C, Keren B, Courtin T, Agrawal PB, Beggs AH, Yu TW. Harris HK, et al. Among authors: kraus c. Genet Med. 2021 Jun;23(6):1028-1040. doi: 10.1038/s41436-021-01114-z. Epub 2021 Mar 3. Genet Med. 2021. PMID: 33658631 Free PMC article.
The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy.
Hebebrand M, Hüffmeier U, Trollmann R, Hehr U, Uebe S, Ekici AB, Kraus C, Krumbiegel M, Reis A, Thiel CT, Popp B. Hebebrand M, et al. Among authors: kraus c. Orphanet J Rare Dis. 2019 Feb 11;14(1):38. doi: 10.1186/s13023-019-1020-x. Orphanet J Rare Dis. 2019. PMID: 30744660 Free PMC article. Review.
Vulvar biopsy reimbursement rates.
Kraus CN, Edwards L. Kraus CN, et al. Int J Womens Dermatol. 2022 Jul 5;8(3):e031. doi: 10.1097/JW9.0000000000000031. eCollection 2022 Oct. Int J Womens Dermatol. 2022. PMID: 36339488 Free PMC article. No abstract available.
543 results