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Results by year

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

Year Number of Results
1949 1
1950 3
1951 3
1952 3
1954 1
1955 2
1957 5
1958 5
1959 2
1960 3
1961 4
1962 2
1963 5
1964 13
1965 5
1966 7
1968 12
1969 3
1970 11
1971 9
1972 10
1973 11
1974 2
1975 8
1976 8
1977 9
1978 4
1979 10
1980 9
1981 10
1982 4
1983 9
1984 15
1985 7
1986 13
1987 17
1988 11
1989 16
1990 9
1991 16
1992 16
1993 16
1994 23
1995 18
1996 13
1997 13
1998 10
1999 16
2000 9
2001 16
2002 10
2003 18
2004 16
2005 22
2006 22
2007 26
2008 27
2009 24
2010 30
2011 26
2012 48
2013 45
2014 63
2015 81
2016 76
2017 82
2018 92
2019 75
2020 100
2021 125
2022 139
2023 121

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Search Results

1,566 results

Results by year

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Page 1
Aortic Valve Stenosis: From Basic Mechanisms to Novel Therapeutic Targets.
Goody PR, Hosen MR, Christmann D, Niepmann ST, Zietzer A, Adam M, Bönner F, Zimmer S, Nickenig G, Jansen F. Goody PR, et al. Among authors: adam m. Arterioscler Thromb Vasc Biol. 2020 Apr;40(4):885-900. doi: 10.1161/ATVBAHA.119.313067. Epub 2020 Mar 12. Arterioscler Thromb Vasc Biol. 2020. PMID: 32160774 Free article. Review.
Mowat-Wilson Syndrome.
Adam MP, Conta J, Bean LJH. Adam MP, et al. 2007 Mar 28 [updated 2019 Jul 25]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2007 Mar 28 [updated 2019 Jul 25]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 20301585 Free Books & Documents. Review.
Fibroblast inflammatory priming determines regenerative versus fibrotic skin repair in reindeer.
Sinha S, Sparks HD, Labit E, Robbins HN, Gowing K, Jaffer A, Kutluberk E, Arora R, Raredon MSB, Cao L, Swanson S, Jiang P, Hee O, Pope H, Workentine M, Todkar K, Sharma N, Bharadia S, Chockalingam K, de Almeida LGN, Adam M, Niklason L, Potter SS, Seifert AW, Dufour A, Gabriel V, Rosin NL, Stewart R, Muench G, McCorkell R, Matyas J, Biernaskie J. Sinha S, et al. Among authors: adam m. Cell. 2022 Dec 8;185(25):4717-4736.e25. doi: 10.1016/j.cell.2022.11.004. Cell. 2022. PMID: 36493752 Free article.
From Genotype to Phenotype-A Review of Kabuki Syndrome.
Barry KK, Tsaparlis M, Hoffman D, Hartman D, Adam MP, Hung C, Bodamer OA. Barry KK, et al. Among authors: adam mp. Genes (Basel). 2022 Sep 29;13(10):1761. doi: 10.3390/genes13101761. Genes (Basel). 2022. PMID: 36292647 Free PMC article. Review.
Design of amidobenzimidazole STING receptor agonists with systemic activity.
Ramanjulu JM, Pesiridis GS, Yang J, Concha N, Singhaus R, Zhang SY, Tran JL, Moore P, Lehmann S, Eberl HC, Muelbaier M, Schneck JL, Clemens J, Adam M, Mehlmann J, Romano J, Morales A, Kang J, Leister L, Graybill TL, Charnley AK, Ye G, Nevins N, Behnia K, Wolf AI, Kasparcova V, Nurse K, Wang L, Puhl AC, Li Y, Klein M, Hopson CB, Guss J, Bantscheff M, Bergamini G, Reilly MA, Lian Y, Duffy KJ, Adams J, Foley KP, Gough PJ, Marquis RW, Smothers J, Hoos A, Bertin J. Ramanjulu JM, et al. Among authors: adam m. Nature. 2018 Dec;564(7736):439-443. doi: 10.1038/s41586-018-0705-y. Epub 2018 Nov 7. Nature. 2018. PMID: 30405246
Astrocyte-neuron crosstalk through Hedgehog signaling mediates cortical synapse development.
Xie Y, Kuan AT, Wang W, Herbert ZT, Mosto O, Olukoya O, Adam M, Vu S, Kim M, Tran D, Gómez N, Charpentier C, Sorour I, Lacey TE, Tolstorukov MY, Sabatini BL, Lee WA, Harwell CC. Xie Y, et al. Among authors: adam m. Cell Rep. 2022 Feb 22;38(8):110416. doi: 10.1016/j.celrep.2022.110416. Cell Rep. 2022. PMID: 35196485 Free PMC article.
Kabuki syndrome: international consensus diagnostic criteria.
Adam MP, Banka S, Bjornsson HT, Bodamer O, Chudley AE, Harris J, Kawame H, Lanpher BC, Lindsley AW, Merla G, Miyake N, Okamoto N, Stumpel CT, Niikawa N; Kabuki Syndrome Medical Advisory Board. Adam MP, et al. J Med Genet. 2019 Feb;56(2):89-95. doi: 10.1136/jmedgenet-2018-105625. Epub 2018 Dec 4. J Med Genet. 2019. PMID: 30514738
Targeted long-read sequencing identifies missing disease-causing variation.
Miller DE, Sulovari A, Wang T, Loucks H, Hoekzema K, Munson KM, Lewis AP, Fuerte EPA, Paschal CR, Walsh T, Thies J, Bennett JT, Glass I, Dipple KM, Patterson K, Bonkowski ES, Nelson Z, Squire A, Sikes M, Beckman E, Bennett RL, Earl D, Lee W, Allikmets R, Perlman SJ, Chow P, Hing AV, Wenger TL, Adam MP, Sun A, Lam C, Chang I, Zou X, Austin SL, Huggins E, Safi A, Iyengar AK, Reddy TE, Majoros WH, Allen AS, Crawford GE, Kishnani PS; University of Washington Center for Mendelian Genomics; King MC, Cherry T, Chong JX, Bamshad MJ, Nickerson DA, Mefford HC, Doherty D, Eichler EE. Miller DE, et al. Among authors: adam mp. Am J Hum Genet. 2021 Aug 5;108(8):1436-1449. doi: 10.1016/j.ajhg.2021.06.006. Epub 2021 Jul 2. Am J Hum Genet. 2021. PMID: 34216551 Free PMC article.
1,566 results