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Results by year

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

Year Number of Results
1927 1
1965 1
1966 3
1967 3
1968 1
1969 2
1970 6
1971 6
1972 9
1973 5
1974 5
1975 9
1976 6
1977 12
1978 13
1979 10
1980 7
1981 13
1982 13
1983 16
1984 12
1985 12
1986 19
1987 17
1988 19
1989 6
1990 18
1991 16
1992 16
1993 15
1994 10
1995 15
1996 25
1997 26
1998 18
1999 22
2000 21
2001 18
2002 14
2003 13
2004 18
2005 30
2006 34
2007 48
2008 43
2009 59
2010 58
2011 68
2012 77
2013 82
2014 91
2015 106
2016 99
2017 98
2018 130
2019 122
2020 151
2021 148
2022 152
2023 146
2024 41

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2,050 results

Results by year

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Page 1
Trial of Erythropoietin for Hypoxic-Ischemic Encephalopathy in Newborns.
Wu YW, Comstock BA, Gonzalez FF, Mayock DE, Goodman AM, Maitre NL, Chang T, Van Meurs KP, Lampland AL, Bendel-Stenzel E, Mathur AM, Wu TW, Riley D, Mietzsch U, Chalak L, Flibotte J, Weitkamp JH, Ahmad KA, Yanowitz TD, Baserga M, Poindexter BB, Rogers EE, Lowe JR, Kuban KCK, O'Shea TM, Wisnowski JL, McKinstry RC, Bluml S, Bonifacio S, Benninger KL, Rao R, Smyser CD, Sokol GM, Merhar S, Schreiber MD, Glass HC, Heagerty PJ, Juul SE; HEAL Consortium. Wu YW, et al. Among authors: mathur am. N Engl J Med. 2022 Jul 14;387(2):148-159. doi: 10.1056/NEJMoa2119660. N Engl J Med. 2022. PMID: 35830641 Free PMC article. Clinical Trial.
Mild hypoxic-ischemic encephalopathy (HIE): timing and pattern of MRI brain injury.
Li Y, Wisnowski JL, Chalak L, Mathur AM, McKinstry RC, Licona G, Mayock DE, Chang T, Van Meurs KP, Wu TW, Ahmad KA, Cornet MC, Rao R, Scheffler A, Wu YW. Li Y, et al. Among authors: mathur am. Pediatr Res. 2022 Dec;92(6):1731-1736. doi: 10.1038/s41390-022-02026-7. Epub 2022 Mar 30. Pediatr Res. 2022. PMID: 35354930 Free PMC article.
A single NGS-based assay covering the entire genomic sequence of the DMD gene facilitates diagnostic and newborn screening confirmatory testing.
Nallamilli BRR, Chaubey A, Valencia CA, Stansberry L, Behlmann AM, Ma Z, Mathur A, Shenoy S, Ganapathy V, Jagannathan L, Ramachander V, Ferlini A, Bean L, Hegde M. Nallamilli BRR, et al. Among authors: mathur a. Hum Mutat. 2021 May;42(5):626-638. doi: 10.1002/humu.24191. Epub 2021 Mar 19. Hum Mutat. 2021. PMID: 33644936
Authors' reply.
Mathur A, Johnston G, Clark L. Mathur A, et al. J R Coll Physicians Edinb. 2020 Jun;50(2):343-350. doi: 10.4997/JRCPE.2020.335. J R Coll Physicians Edinb. 2020. PMID: 32936125 No abstract available.
Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in India.
Narang A, Uppilli B, Vivekanand A, Naushin S, Yadav A, Singhal K, Shamim U, Sharma P, Zahra S, Mathur A, Seth M, Parveen S, Vats A, Hillman S, Dolma P, Varma B, Jain V; TRISUTRA Ayurgenomics Consortium; Prasher B, Sengupta S, Mukerji M, Faruq M. Narang A, et al. Among authors: mathur a. Hum Mutat. 2020 Nov;41(11):1833-1847. doi: 10.1002/humu.24102. Epub 2020 Sep 9. Hum Mutat. 2020. PMID: 32906206
Pulmonary sarcoidosis: a clinical update.
Hu MK, Mathur A, Dempsey OJ. Hu MK, et al. Among authors: mathur a. J R Coll Physicians Edinb. 2020 Sep;50(3):322-329. doi: 10.4997/JRCPE.2020.324. J R Coll Physicians Edinb. 2020. PMID: 32936114 Review.
Anemia of prematurity: how low is too low?
Cibulskis CC, Maheshwari A, Rao R, Mathur AM. Cibulskis CC, et al. Among authors: mathur am. J Perinatol. 2021 Jun;41(6):1244-1257. doi: 10.1038/s41372-021-00992-0. Epub 2021 Mar 4. J Perinatol. 2021. PMID: 33664467 Review.
2,050 results