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

Year Number of Results
1993 1
2005 2
2006 8
2007 4
2008 1
2009 3
2010 3
2011 5
2012 13
2013 8
2014 14
2015 18
2016 16
2017 11
2018 17
2019 12
2020 11
2021 11
2022 13
2023 16
2024 11

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162 results

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Page 1
Molecular diagnostics.
Kesari A, Dalal A, Lal G, Pandey SN. Kesari A, et al. Among authors: dalal a. Biomed Res Int. 2013;2013:387486. doi: 10.1155/2013/387486. Epub 2013 Sep 3. Biomed Res Int. 2013. PMID: 24078915 Free PMC article. No abstract available.
Progressive Pseudorheumatoid Dysplasia.
Bhavani GS, Shah H, Shukla A, Dalal A, Girisha KM. Bhavani GS, et al. Among authors: dalal a. 2015 Nov 25 [updated 2020 Dec 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2015 Nov 25 [updated 2020 Dec 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 26610319 Free Books & Documents. Review.
Dental stem cells: Hope or hype?
Dalal A. Dalal A. Indian J Dent Res. 2016 Mar-Apr;27(2):113-4. doi: 10.4103/0970-9290.183118. Indian J Dent Res. 2016. PMID: 27237197 Free article. No abstract available.
Hemihyperplasia syndromes.
Dalal AB, Phadke SR, Pradhan M, Sharda S. Dalal AB, et al. Indian J Pediatr. 2006 Jul;73(7):609-15. doi: 10.1007/BF02759927. Indian J Pediatr. 2006. PMID: 16877856
Neuromuscular disease genetics in under-represented populations: increasing data diversity.
Wilson LA, Macken WL, Perry LD, Record CJ, Schon KR, Frezatti RSS, Raga S, Naidu K, Köken ÖY, Polat I, Kapapa MM, Dominik N, Efthymiou S, Morsy H, Nel M, Fassad MR, Gao F, Patel K, Schoonen M, Bisschoff M, Vorster A, Jonvik H, Human R, Lubbe E, Nonyane M, Vengalil S, Nashi S, Srivastava K, Lemmers RJLF, Reyaz A, Mishra R, Töpf A, Trainor CI, Steyn EC, Mahungu AC, van der Vliet PJ, Ceylan AC, Hiz AS, Çavdarlı B, Semerci Gündüz CN, Ceylan GG, Nagappa M, Tallapaka KB, Govindaraj P, van der Maarel SM, Narayanappa G, Nandeesh BN, Wa Somwe S, Bearden DR, Kvalsund MP, Ramdharry GM, Oktay Y, Yiş U, Topaloğlu H, Sarkozy A, Bugiardini E, Henning F, Wilmshurst JM, Heckmann JM, McFarland R, Taylor RW, Smuts I, van der Westhuizen FH, Sobreira CFDR, Tomaselli PJ, Marques W Jr, Bhatia R, Dalal A, Srivastava MVP, Yareeda S, Nalini A, Vishnu VY, Thangaraj K, Straub V, Horvath R, Chinnery PF, Pitceathly RDS, Muntoni F, Houlden H, Vandrovcova J, Reilly MM, Hanna MG. Wilson LA, et al. Among authors: dalal a. Brain. 2023 Dec 1;146(12):5098-5109. doi: 10.1093/brain/awad254. Brain. 2023. PMID: 37516995 Free PMC article.
Mitochondria in biology and medicine - 2023.
Disha B, Mathew RP, Dalal AB, Mahato AK, Satyamoorthy K, Singh KK, Thangaraj K, Govindaraj P. Disha B, et al. Among authors: dalal ab. Mitochondrion. 2024 May;76:101853. doi: 10.1016/j.mito.2024.101853. Epub 2024 Feb 28. Mitochondrion. 2024. PMID: 38423268 Review.
Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrum.
Priestley JRC, Deshwar AR, Murthy H, D'Agostino MD, Dupuis L, Gangaram B, Gray C, Jobling R, Pannia E, Platzer K, Prescott K, Redman M, Rippert AL, Rosenfeld JA, Scott DA, Wang YW, Schmederer Z, Dalal A, Sarma AS, Skraban C, Dowling JJ, Mendoza-Londono R, Slavotinek A, Bhoj EJ. Priestley JRC, et al. Among authors: dalal a. Genet Med. 2023 Aug;25(8):100863. doi: 10.1016/j.gim.2023.100863. Epub 2023 Apr 28. Genet Med. 2023. PMID: 37125634
Two sisters with RSPRY1-related spondyloepimetaphyseal dysplasia.
Singh S, Shah H, Dalal A, Shukla A, Bhavani GS, Girisha KM. Singh S, et al. Among authors: dalal a. Am J Med Genet A. 2024 Apr 2:e63601. doi: 10.1002/ajmg.a.63601. Online ahead of print. Am J Med Genet A. 2024. PMID: 38562122
Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13.
Jacob P, Lindelöf H, Rustad CF, Sutton VR, Moosa S, Udupa P, Hammarsjö A, Bhavani GS, Batkovskyte D, Tveten K, Dalal A, Horemuzova E, Nordgren A, Tham E, Shah H, Merckoll E, Orellana L, Nishimura G, Girisha KM, Grigelioniene G. Jacob P, et al. Among authors: dalal a. NPJ Genom Med. 2023 Nov 22;8(1):39. doi: 10.1038/s41525-023-00380-x. NPJ Genom Med. 2023. PMID: 37993442 Free PMC article.
Exome Sequencing in Monogenic Forms of Rickets.
Jacob P, Bhavani GS, Udupa P, Wang Z, Hariharan SV, Delampady K, Dalal A, Kamath N, Ikegawa S, Shenoy RD, Handattu K, Shah H, Girisha KM. Jacob P, et al. Among authors: dalal a. Indian J Pediatr. 2023 Dec;90(12):1182-1190. doi: 10.1007/s12098-022-04393-9. Epub 2023 Jan 24. Indian J Pediatr. 2023. PMID: 36692815 Free PMC article.
162 results