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

Year Number of Results
1996 2
1999 1
2000 3
2001 5
2002 2
2005 1
2006 2
2007 6
2008 2
2009 2
2010 3
2011 14
2012 16
2013 13
2014 9
2015 5
2016 4
2017 3
2018 3
2019 6
2020 12
2021 22
2022 2
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120 results
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Page 1
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla JA, Eichler EE, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RM, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, Martin CL, Ledbetter DH. Miller DT, et al. Among authors: aradhya s. Am J Hum Genet. 2010 May 14;86(5):749-64. doi: 10.1016/j.ajhg.2010.04.006. Am J Hum Genet. 2010. PMID: 20466091 Free PMC article. Review.
Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
Riggs ER, Andersen EF, Cherry AM, Kantarci S, Kearney H, Patel A, Raca G, Ritter DI, South ST, Thorland EC, Pineda-Alvarez D, Aradhya S, Martin CL. Riggs ER, et al. Among authors: aradhya s. Genet Med. 2020 Feb;22(2):245-257. doi: 10.1038/s41436-019-0686-8. Epub 2019 Nov 6. Genet Med. 2020. PMID: 31690835 Free PMC article.
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Kaminsky EB, Kaul V, Paschall J, Church DM, Bunke B, Kunig D, Moreno-De-Luca D, Moreno-De-Luca A, Mulle JG, Warren ST, Richard G, Compton JG, Fuller AE, Gliem TJ, Huang S, Collinson MN, Beal SJ, Ackley T, Pickering DL, Golden DM, Aston E, Whitby H, Shetty S, Rossi MR, Rudd MK, South ST, Brothman AR, Sanger WG, Iyer RK, Crolla JA, Thorland EC, Aradhya S, Ledbetter DH, Martin CL. Kaminsky EB, et al. Among authors: aradhya s. Genet Med. 2011 Sep;13(9):777-84. doi: 10.1097/GIM.0b013e31822c79f9. Genet Med. 2011. PMID: 21844811 Free PMC article.
Response to Maya et al.
Riggs ER, Andersen EF, Kantarci S, Kearney H, Patel A, Raca G, Ritter DI, South ST, Thorland EC, Pineda-Alvarez D, Aradhya S, Martin CL; American College of Medical Genetics and Genomics. Riggs ER, et al. Among authors: aradhya s. Genet Med. 2020 Jul;22(7):1278-1279. doi: 10.1038/s41436-020-0796-3. Epub 2020 Apr 28. Genet Med. 2020. PMID: 32341575 No abstract available.
Indian Dermatologists Wield Technology to Combat COVID-19!
Jakhar D, Sharma A, Kaur I, Sharma R, Das A, Madke B, Jindal V, Aradhya SS, Mhatre M. Jakhar D, et al. Among authors: aradhya ss. Indian Dermatol Online J. 2020 Sep 19;11(6):991-994. doi: 10.4103/idoj.IDOJ_292_20. eCollection 2020 Nov-Dec. Indian Dermatol Online J. 2020. PMID: 33344354 Free PMC article. No abstract available.
Clinical outcome of collodion baby: a retrospective review.
Aradhya SS, Srinivas SM, Hiremagalore R, Shanmukappa AG. Aradhya SS, et al. Indian J Dermatol Venereol Leprol. 2013 Jul-Aug;79(4):553. doi: 10.4103/0378-6323.113110. Indian J Dermatol Venereol Leprol. 2013. PMID: 23760337 Free article. Review. No abstract available.
NF-kappaB signaling and human disease.
Aradhya S, Nelson DL. Aradhya S, et al. Curr Opin Genet Dev. 2001 Jun;11(3):300-6. doi: 10.1016/s0959-437x(00)00194-5. Curr Opin Genet Dev. 2001. PMID: 11377967 Review.
Easing the Excision of Earlobe Keloid.
Prasad BRH, Leelavathy B, Aradhya SS, Shilpa K, Vasudevan B. Prasad BRH, et al. Among authors: aradhya ss. J Cutan Aesthet Surg. 2017 Jul-Sep;10(3):168-171. doi: 10.4103/JCAS.JCAS_122_16. J Cutan Aesthet Surg. 2017. PMID: 29403191 Free PMC article.
120 results