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

Year Number of Results
1952 1
1960 1
1962 1
1963 1
1964 1
1967 3
1968 2
1969 5
1970 9
1971 10
1972 8
1973 13
1974 11
1975 83
1976 78
1977 77
1978 93
1979 103
1980 108
1981 148
1982 159
1983 226
1984 237
1985 349
1986 367
1987 424
1988 598
1989 764
1990 1027
1991 1163
1992 1416
1993 1694
1994 1917
1995 2330
1996 2607
1997 2972
1998 3413
1999 4003
2000 4592
2001 5042
2002 5307
2003 5981
2004 6725
2005 7558
2006 8316
2007 9030
2008 9845
2009 10423
2010 11952
2011 13071
2012 14258
2013 15597
2014 15987
2015 16149
2016 15756
2017 16216
2018 16131
2019 16709
2020 17816
2021 17976
2022 17011
2023 15545
2024 5205

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290,296 results

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Page 1
Cancer Epigenetics: An Overview.
Recillas-Targa F. Recillas-Targa F. Arch Med Res. 2022 Dec;53(8):732-740. doi: 10.1016/j.arcmed.2022.11.003. Epub 2022 Nov 18. Arch Med Res. 2022. PMID: 36411173 Review.
Cancer is a complex disease caused by genetic and epigenetic alterations in the control of cell division. Findings from the field of cancer genomics and epigenomics have increased our understanding of the origin and evolution of tumorigenic processes, greatly advanc …
Cancer is a complex disease caused by genetic and epigenetic alterations in the control of cell division. Findings from the fi …
Ischemia/Reperfusion.
Kalogeris T, Baines CP, Krenz M, Korthuis RJ. Kalogeris T, et al. Compr Physiol. 2016 Dec 6;7(1):113-170. doi: 10.1002/cphy.c160006. Compr Physiol. 2016. PMID: 28135002 Free PMC article. Review.
Ischemic disorders, such as myocardial infarction, stroke, and peripheral vascular disease, are the most common causes of debilitating disease and death in westernized cultures. ...By impairing ATPase-dependent ion transport, ischemia causes intracellular and …
Ischemic disorders, such as myocardial infarction, stroke, and peripheral vascular disease, are the most common causes of debi …
Nutrition and Genetics in NAFLD: The Perfect Binomium.
Meroni M, Longo M, Rustichelli A, Dongiovanni P. Meroni M, et al. Int J Mol Sci. 2020 Apr 23;21(8):2986. doi: 10.3390/ijms21082986. Int J Mol Sci. 2020. PMID: 32340286 Free PMC article. Review.
Nonalcoholic fatty liver disease (NAFLD) represents a global healthcare burden since it is epidemiologically related to obesity, type 2 diabetes (T2D) and Metabolic Syndrome (MetS). It embraces a wide spectrum of hepatic injuries, which include simple steatosis, nonalcohol …
Nonalcoholic fatty liver disease (NAFLD) represents a global healthcare burden since it is epidemiologically related to obesity, type 2 diab …
Genetic contributions to autism spectrum disorder.
Havdahl A, Niarchou M, Starnawska A, Uddin M, van der Merwe C, Warrier V. Havdahl A, et al. Psychol Med. 2021 Oct;51(13):2260-2273. doi: 10.1017/S0033291721000192. Epub 2021 Feb 26. Psychol Med. 2021. PMID: 33634770 Free PMC article. Review.
Studies have identified a handful of robustly associated common variants. Different risk genes converge on the same mechanisms, such as gene regulation and synaptic connectivity. ...Considerable increases in sample sizes are needed to better understand the hundreds or thou …
Studies have identified a handful of robustly associated common variants. Different risk genes converge on the same mechanisms, such …
Comparison and validation of the 2022 European LeukemiaNet guidelines in acute myeloid leukemia.
Lachowiez CA, Long N, Saultz J, Gandhi A, Newell LF, Hayes-Lattin B, Maziarz RT, Leonard J, Bottomly D, McWeeney S, Dunlap J, Press R, Meyers G, Swords R, Cook RJ, Tyner JW, Druker BJ, Traer E. Lachowiez CA, et al. Blood Adv. 2023 May 9;7(9):1899-1909. doi: 10.1182/bloodadvances.2022009010. Blood Adv. 2023. PMID: 36441905 Free PMC article.
This comparative analysis evaluated outcomes between the 2017 and 2022 ELN criteria in patients enrolled within the multicenter Beat AML cohort. Five hundred thirteen patients were included. Most patients had 1 or 2 ELN risk-defining abnormalities. ...Compared with ELN 201 …
This comparative analysis evaluated outcomes between the 2017 and 2022 ELN criteria in patients enrolled within the multicenter Beat AML coh …
Obesity in Toddlers and Young Children: Causes and Consequences.
Singhal A. Singhal A. Nestle Nutr Inst Workshop Ser. 2020;95:41-51. doi: 10.1159/000511510. Epub 2020 Nov 6. Nestle Nutr Inst Workshop Ser. 2020. PMID: 33161404 Review.
Most research has focused on biological risk factors, which can be broadly categorized as genetic predisposition, poor diet (and the behaviors that influence excessive food intake), insufficient physical activity, and the role of developmental factors …
Most research has focused on biological risk factors, which can be broadly categorized as genetic predisposition, poor diet (a …
Periorbital Hyperpigmentation: A Comprehensive Review.
Sarkar R, Ranjan R, Garg S, Garg VK, Sonthalia S, Bansal S. Sarkar R, et al. J Clin Aesthet Dermatol. 2016 Jan;9(1):49-55. J Clin Aesthet Dermatol. 2016. PMID: 26962392 Free PMC article.
Periorbital hyperpigmentation is caused by various exogenous and endogenous factors. The causative factors include genetic or heredity, excessive pigmentation, postinflammatory hyperpigmentatio …
Periorbital hyperpigmentation is caused by various exogenous and endogenous factors. The causative fac …
Genetics of primary ovarian insufficiency: new developments and opportunities.
Qin Y, Jiao X, Simpson JL, Chen ZJ. Qin Y, et al. Hum Reprod Update. 2015 Nov-Dec;21(6):787-808. doi: 10.1093/humupd/dmv036. Epub 2015 Aug 4. Hum Reprod Update. 2015. PMID: 26243799 Free PMC article. Review.
BACKGROUND: Primary ovarian insufficiency (POI) is characterized by marked heterogeneity, but with a significant genetic contribution. Identifying exact causative genes has been challenging, with many discoveries not replicated. It is timely to take stock of the fie …
BACKGROUND: Primary ovarian insufficiency (POI) is characterized by marked heterogeneity, but with a significant genetic contribution …
Ischemic Stroke Genetics: What Is New and How to Apply It in Clinical Practice?
Ekkert A, Šliachtenko A, Grigaitė J, Burnytė B, Utkus A, Jatužis D. Ekkert A, et al. Genes (Basel). 2021 Dec 24;13(1):48. doi: 10.3390/genes13010048. Genes (Basel). 2021. PMID: 35052389 Free PMC article. Review.
The etiology of ischemic stroke is multifactorial. Although receiving less emphasis, genetic causes make a significant contribution to ischemic stroke genesis, especially in early-onset stroke. ...Some monogenic disorders, despite covering only about 7% of st …
The etiology of ischemic stroke is multifactorial. Although receiving less emphasis, genetic causes make a significant …
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Linder JE, Allworth A, Bland HT, Caraballo PJ, Chisholm RL, Clayton EW, Crosslin DR, Dikilitas O, DiVietro A, Esplin ED, Forman S, Freimuth RR, Gordon AS, Green R, Harden MV, Holm IA, Jarvik GP, Karlson EW, Labrecque S, Lennon NJ, Limdi NA, Mittendorf KF, Murphy SN, Orlando L, Prows CA, Rasmussen LV, Rasmussen-Torvik L, Rowley R, Sawicki KT, Schmidlen T, Terek S, Veenstra D, Velez Edwards DR, Absher D, Abul-Husn NS, Alsip J, Bangash H, Beasley M, Below JE, Berner ES, Booth J, Chung WK, Cimino JJ, Connolly J, Davis P, Devine B, Fullerton SM, Guiducci C, Habrat ML, Hain H, Hakonarson H, Harr M, Haverfield E, Hernandez V, Hoell C, Horike-Pyne M, Hripcsak G, Irvin MR, Kachulis C, Karavite D, Kenny EE, Khan A, Kiryluk K, Korf B, Kottyan L, Kullo IJ, Larkin K, Liu C, Malolepsza E, Manolio TA, May T, McNally EM, Mentch F, Miller A, Mooney SD, Murali P, Mutai B, Muthu N, Namjou B, Perez EF, Puckelwartz MJ, Rakhra-Burris T, Roden DM, Rosenthal EA, Saadatagah S, Sabatello M, Schaid DJ, Schultz B, Seabolt L, Shaibi GQ, Sharp RR, Shirts B, Smith ME, Smoller JW, Sterling R, Suckiel SA, Thayer J, Tiwari HK, Trinidad SB, Walunas T, Wei WQ, Wells QS, Weng C, Wiesner GL, Wiley K; eMERGE Consortium… See abstract for full author list ➔ Linder JE, et al. Genet Med. 2023 Apr;25(4):100006. doi: 10.1016/j.gim.2023.100006. Epub 2023 Jan 6. Genet Med. 2023. PMID: 36621880 Free PMC article.
Returning risks to individuals and providers may influence preventive care or use of prophylactic therapies for those individuals at high genetic risk. METHODS: To enable integrated genetic risk assessment, the eMERGE (electronic MEdical Records and GEnomics) networ …
Returning risks to individuals and providers may influence preventive care or use of prophylactic therapies for those individuals at high …
290,296 results
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