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

Year Number of Results
1930 1
1937 1
1945 1
1948 2
1949 1
1951 1
1952 1
1953 4
1954 1
1955 5
1957 3
1958 2
1959 6
1960 1
1961 1
1962 5
1963 4
1964 7
1965 6
1966 4
1968 1
1969 4
1970 2
1971 2
1972 4
1973 2
1974 3
1975 1
1976 2
1977 4
1978 6
1979 5
1980 9
1981 5
1982 3
1983 8
1984 14
1985 9
1986 14
1987 7
1988 11
1989 12
1990 12
1991 8
1992 14
1993 14
1994 21
1995 10
1996 14
1997 16
1998 13
1999 13
2000 20
2001 14
2002 10
2003 15
2004 16
2005 22
2006 33
2007 33
2008 43
2009 35
2010 29
2011 27
2012 49
2013 53
2014 58
2015 52
2016 50
2017 50
2018 57
2019 71
2020 113
2021 119
2022 12
Text availability
Article attribute
Article type
Publication date

Search Results

1,190 results
Results by year
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Page 1
Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease.
Kim J, Hu C, Moufawad El Achkar C, Black LE, Douville J, Larson A, Pendergast MK, Goldkind SF, Lee EA, Kuniholm A, Soucy A, Vaze J, Belur NR, Fredriksen K, Stojkovska I, Tsytsykova A, Armant M, DiDonato RL, Choi J, Cornelissen L, Pereira LM, Augustine EF, Genetti CA, Dies K, Barton B, Williams L, Goodlett BD, Riley BL, Pasternak A, Berry ER, Pflock KA, Chu S, Reed C, Tyndall K, Agrawal PB, Beggs AH, Grant PE, Urion DK, Snyder RO, Waisbren SE, Poduri A, Park PJ, Patterson A, Biffi A, Mazzulli JR, Bodamer O, Berde CB, Yu TW. Kim J, et al. Among authors: larson a. N Engl J Med. 2019 Oct 24;381(17):1644-1652. doi: 10.1056/NEJMoa1813279. Epub 2019 Oct 9. N Engl J Med. 2019. PMID: 31597037 Free PMC article.
Glutaric Acidemia Type 1.
Larson A, Goodman S. Larson A, et al. 2019 Sep 19. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviewsĀ® [Internet]. Seattle (WA): University of Washington, Seattle; 1993ā€“2022. 2019 Sep 19. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviewsĀ® [Internet]. Seattle (WA): University of Washington, Seattle; 1993ā€“2022. PMID: 31536184 Free Books & Documents. Review.
Pediatric Ankle Fractures: Concepts and Treatment Principles.
Su AW, Larson AN. Su AW, et al. Among authors: larson an. Foot Ankle Clin. 2015 Dec;20(4):705-19. doi: 10.1016/j.fcl.2015.07.004. Epub 2015 Oct 16. Foot Ankle Clin. 2015. PMID: 26589088 Free PMC article. Review.
Natural History of Slipped Capital Femoral Epiphysis.
Mathew SE, Larson AN. Mathew SE, et al. Among authors: larson an. J Pediatr Orthop. 2019 Jul;39(Issue 6, Supplement 1 Suppl 1):S23-S27. doi: 10.1097/BPO.0000000000001369. J Pediatr Orthop. 2019. PMID: 31169643 Review.
De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder.
Mirzaa GM, Chong JX, Piton A, Popp B, Foss K, Guo H, Harripaul R, Xia K, Scheck J, Aldinger KA, Sajan SA, Tang S, Bonneau D, Beck A, White J, Mahida S, Harris J, Smith-Hicks C, Hoyer J, Zweier C, Reis A, Thiel CT, Jamra RA, Zeid N, Yang A, Farach LS, Walsh L, Payne K, Rohena L, Velinov M, Ziegler A, Schaefer E, Gatinois V, GeneviĆØve D, Simon MEH, Kohler J, Rotenberg J, Wheeler P, Larson A, Ernst ME, Akman CI, Westman R, Blanchet P, Schillaci LA, Vincent-Delorme C, Gripp KW, Mattioli F, Guyader GL, Gerard B, Mathieu-Dramard M, Morin G, Sasanfar R, Ayub M, Vasli N, Yang S, Person R, Monaghan KG, Nickerson DA, van Binsbergen E, Enns GM, Dries AM, Rowe LJ, Tsai ACH, Svihovec S, Friedman J, Agha Z, Qamar R, Rodan LH, Martinez-Agosto J, Ockeloen CW, Vincent M, Sunderland WJ, Bernstein JA; Undiagnosed Diseases Network,, Eichler EE, Vincent JB; University of Washington Center for Mendelian Genomics (UW-CMG),, Bamshad MJ. Mirzaa GM, et al. Among authors: larson a. Genet Med. 2020 Mar;22(3):538-546. doi: 10.1038/s41436-019-0693-9. Epub 2019 Nov 14. Genet Med. 2020. PMID: 31723249 Free PMC article.
Reply.
Larson AS, Brinjikji W. Larson AS, et al. AJNR Am J Neuroradiol. 2021 Apr;42(4):E28. doi: 10.3174/ajnr.A6986. Epub 2021 Mar 4. AJNR Am J Neuroradiol. 2021. PMID: 33664104 No abstract available.
De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay.
Vissers LELM, Kalvakuri S, de Boer E, Geuer S, Oud M, van Outersterp I, Kwint M, Witmond M, Kersten S, Polla DL, Weijers D, Begtrup A, McWalter K, Ruiz A, Gabau E, Morton JEV, Griffith C, Weiss K, Gamble C, Bartley J, Vernon HJ, Brunet K, Ruivenkamp C, Kant SG, Kruszka P, Larson A, Afenjar A, Billette de Villemeur T, Nugent K; DDD Study, Raymond FL, Venselaar H, Demurger F, Soler-Alfonso C, Li D, Bhoj E, Hayes I, Hamilton NP, Ahmad A, Fisher R, van den Born M, Willems M, Sorlin A, Delanne J, Moutton S, Christophe P, Mau-Them FT, Vitobello A, Goel H, Massingham L, Phornphutkul C, Schwab J, Keren B, Charles P, Vreeburg M, De Simone L, Hoganson G, Iascone M, Milani D, Evenepoel L, Revencu N, Ward DI, Burns K, Krantz I, Raible SE, Murrell JR, Wood K, Cho MT, van Bokhoven H, Muenke M, Kleefstra T, Bodmer R, de Brouwer APM. Vissers LELM, et al. Among authors: larson a. Am J Hum Genet. 2020 Jul 2;107(1):164-172. doi: 10.1016/j.ajhg.2020.05.017. Epub 2020 Jun 17. Am J Hum Genet. 2020. PMID: 32553196 Free PMC article.
Transoral Excision of Parapharyngeal Space Tumors.
Larson AR, Ryan WR. Larson AR, et al. Otolaryngol Clin North Am. 2021 Jun;54(3):531-541. doi: 10.1016/j.otc.2021.03.001. Otolaryngol Clin North Am. 2021. PMID: 34024481 Review.
1,190 results