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

Year Number of Results
1946 2
1959 2
1965 2
1966 2
1967 4
1968 5
1969 1
1970 5
1971 4
1972 3
1973 7
1974 12
1975 9
1976 8
1977 5
1978 10
1979 4
1980 6
1981 12
1982 4
1983 12
1984 9
1985 10
1986 11
1987 17
1988 11
1989 22
1990 10
1991 16
1992 32
1993 24
1994 25
1995 23
1996 23
1997 35
1998 27
1999 21
2000 29
2001 22
2002 25
2003 31
2004 26
2005 31
2006 36
2007 39
2008 41
2009 36
2010 53
2011 76
2012 91
2013 106
2014 97
2015 94
2016 112
2017 94
2018 88
2019 82
2020 99
2021 96
2022 7
Text availability
Article attribute
Article type
Publication date

Search Results

1,673 results
Results by year
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Page 1
Current understanding of the human microbiome.
Gilbert JA, Blaser MJ, Caporaso JG, Jansson JK, Lynch SV, Knight R. Gilbert JA, et al. Among authors: lynch sv. Nat Med. 2018 Apr 10;24(4):392-400. doi: 10.1038/nm.4517. Nat Med. 2018. PMID: 29634682 Free PMC article. Review.
Interdisciplinary Care of Children with Severe Bronchopulmonary Dysplasia.
Abman SH, Collaco JM, Shepherd EG, Keszler M, Cuevas-Guaman M, Welty SE, Truog WE, McGrath-Morrow SA, Moore PE, Rhein LM, Kirpalani H, Zhang H, Gratny LL, Lynch SK, Curtiss J, Stonestreet BS, McKinney RL, Dysart KC, Gien J, Baker CD, Donohue PK, Austin E, Fike C, Nelin LD; Bronchopulmonary Dysplasia Collaborative. Abman SH, et al. Among authors: lynch sk. J Pediatr. 2017 Feb;181:12-28.e1. doi: 10.1016/j.jpeds.2016.10.082. Epub 2016 Nov 28. J Pediatr. 2017. PMID: 27908648 Free PMC article. No abstract available.
Acute epididymitis.
Lynch S. Lynch S. JAAPA. 2018 Mar;31(3):50-51. doi: 10.1097/01.JAA.0000530304.69021.4b. JAAPA. 2018. PMID: 29470373 No abstract available.
Further delineation of Malan syndrome.
Priolo M, Schanze D, Tatton-Brown K, Mulder PA, Tenorio J, Kooblall K, Acero IH, Alkuraya FS, Arias P, Bernardini L, Bijlsma EK, Cole T, Coubes C, Dapia I, Davies S, Di Donato N, Elcioglu NH, Fahrner JA, Foster A, González NG, Huber I, Iascone M, Kaiser AS, Kamath A, Liebelt J, Lynch SA, Maas SM, Mammì C, Mathijssen IB, McKee S, Menke LA, Mirzaa GM, Montgomery T, Neubauer D, Neumann TE, Pintomalli L, Pisanti MA, Plomp AS, Price S, Salter C, Santos-Simarro F, Sarda P, Segovia M, Shaw-Smith C, Smithson S, Suri M, Valdez RM, Van Haeringen A, Van Hagen JM, Zollino M, Lapunzina P, Thakker RV, Zenker M, Hennekam RC. Priolo M, et al. Among authors: lynch sa. Hum Mutat. 2018 Sep;39(9):1226-1237. doi: 10.1002/humu.23563. Epub 2018 Jun 25. Hum Mutat. 2018. PMID: 29897170 Free PMC article.
The phenotype of Sotos syndrome in adulthood: A review of 44 individuals.
Foster A, Zachariou A, Loveday C, Ashraf T, Blair E, Clayton-Smith J, Dorkins H, Fryer A, Gener B, Goudie D, Henderson A, Irving M, Joss S, Keeley V, Lahiri N, Lynch SA, Mansour S, McCann E, Morton J, Motton N, Murray A, Riches K, Shears D, Stark Z, Thompson E, Vogt J, Wright M, Cole T, Tatton-Brown K. Foster A, et al. Among authors: lynch sa. Am J Med Genet C Semin Med Genet. 2019 Dec;181(4):502-508. doi: 10.1002/ajmg.c.31738. Epub 2019 Sep 3. Am J Med Genet C Semin Med Genet. 2019. PMID: 31479583 Review.
Biomarkers of Nutrition for Development (BOND)-Iron Review.
Lynch S, Pfeiffer CM, Georgieff MK, Brittenham G, Fairweather-Tait S, Hurrell RF, McArdle HJ, Raiten DJ. Lynch S, et al. J Nutr. 2018 Jun 1;148(suppl_1):1001S-1067S. doi: 10.1093/jn/nxx036. J Nutr. 2018. PMID: 29878148 Free PMC article. Review.
NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families.
Al Shehhi M, Forman EB, Fitzgerald JE, McInerney V, Krawczyk J, Shen S, Betts DR, Ardle LM, Gorman KM, King MD, Green A, Gallagher L, Lynch SA. Al Shehhi M, et al. Among authors: lynch sa. Eur J Med Genet. 2019 Mar;62(3):204-209. doi: 10.1016/j.ejmg.2018.07.015. Epub 2018 Jul 18. Eur J Med Genet. 2019. PMID: 30031152
1,673 results