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

Year Number of Results
1984 1
1985 1
1986 1
1987 3
1988 3
1989 2
1990 3
1991 3
1992 1
1993 1
1996 1
1998 2
1999 1
2000 1
2002 1
2004 1
2005 2
2006 1
2007 5
2008 3
2009 1
2010 1
2011 2
2012 4
2013 4
2014 7
2015 7
2016 12
2017 7
2018 4
2019 9
2020 26
2021 19
2022 12
2023 9
2024 4

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152 results

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Page 1
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Snijders Blok L, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, Nowak CB, Douglas J, Swoboda KJ, Steeves MA, Sahai I, Stumpel CTRM, Stegmann APA, Wheeler P, Willing M, Fiala E, Kochhar A, Gibson WT, Cohen ASA, Agbahovbe R, Innes AM, Au PYB, Rankin J, Anderson IJ, Skinner SA, Louie RJ, Warren HE, Afenjar A, Keren B, Nava C, Buratti J, Isapof A, Rodriguez D, Lewandowski R, Propst J, van Essen T, Choi M, Lee S, Chae JH, Price S, Schnur RE, Douglas G, Wentzensen IM, Zweier C, Reis A, Bialer MG, Moore C, Koopmans M, Brilstra EH, Monroe GR, van Gassen KLI, van Binsbergen E, Newbury-Ecob R, Bownass L, Bader I, Mayr JA, Wortmann SB, Jakielski KJ, Strand EA, Kloth K, Bierhals T; DDD study; Roberts JD, Petrovich RM, Machida S, Kurumizaka H, Lelieveld S, Pfundt R, Jansen S, Deriziotis P, Faivre L, Thevenon J, Assoum M, Shriberg L, Kleefstra T, Brunner HG, Wade PA, Fisher SE, Campeau PM. Snijders Blok L, et al. Among authors: kochhar a. Nat Commun. 2018 Nov 5;9(1):4619. doi: 10.1038/s41467-018-06014-6. Nat Commun. 2018. PMID: 30397230 Free PMC article.
Facial Nerve and Parotid Gland Anatomy.
Kochhar A, Larian B, Azizzadeh B. Kochhar A, et al. Otolaryngol Clin North Am. 2016 Apr;49(2):273-84. doi: 10.1016/j.otc.2015.10.002. Otolaryngol Clin North Am. 2016. PMID: 27040583 Review.
Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders.
Langhammer F, Maroofian R, Badar R, Gregor A, Rochman M, Ratliff JB, Koopmans M, Herget T, Hempel M, Kortüm F, Heron D, Mignot C, Keren B, Brooks S, Botti C, Ben-Zeev B, Argilli E, Sherr EH, Gowda VK, Srinivasan VM, Bakhtiari S, Kruer MC, Salih MA, Kuechler A, Muller EA, Blocker K, Kuismin O, Park KL, Kochhar A, Brown K, Ramanathan S, Clark RD, Elgizouli M, Melikishvili G, Tabatadze N, Stark Z, Mirzaa GM, Ong J, Grasshoff U, Bevot A, von Wintzingerode L, Jamra RA, Hennig Y, Goldenberg P, Al Alam C, Charif M, Boulouiz R, Bellaoui M, Amrani R, Al Mutairi F, Tamim AM, Abdulwahab F, Alkuraya FS, Khouj EM, Alvi JR, Sultan T, Hashemi N, Karimiani EG, Ashrafzadeh F, Imannezhad S, Efthymiou S, Houlden H, Sticht H, Zweier C. Langhammer F, et al. Among authors: kochhar a. Genet Med. 2023 Aug;25(8):100885. doi: 10.1016/j.gim.2023.100885. Epub 2023 May 8. Genet Med. 2023. PMID: 37165955
Delaying Intraoral Radiographs during the COVID-19 Pandemic: A Conundrum.
Kaur H, Gupta H, Dadlani H, Kochhar GK, Singh G, Bhasin R, Kochhar AS, Alam MK. Kaur H, et al. Among authors: kochhar as. Biomed Res Int. 2022 Jan 12;2022:8432856. doi: 10.1155/2022/8432856. eCollection 2022. Biomed Res Int. 2022. PMID: 35036440 Free PMC article. Review.
Vitamin D and skin diseases: A review.
Wadhwa B, Relhan V, Goel K, Kochhar AM, Garg VK. Wadhwa B, et al. Among authors: kochhar am. Indian J Dermatol Venereol Leprol. 2015 Jul-Aug;81(4):344-55. doi: 10.4103/0378-6323.159928. Indian J Dermatol Venereol Leprol. 2015. PMID: 26144849 Free article. Review. No abstract available.
Branchio-oto-renal syndrome.
Kochhar A, Fischer SM, Kimberling WJ, Smith RJ. Kochhar A, et al. Am J Med Genet A. 2007 Jul 15;143A(14):1671-8. doi: 10.1002/ajmg.a.31561. Am J Med Genet A. 2007. PMID: 17238186 Review.
152 results