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

Year Number of Results
2002 5
2004 6
2005 12
2006 2
2007 7
2008 5
2009 6
2010 9
2011 9
2012 7
2013 3
2014 11
2015 10
2016 8
2017 10
2018 12
2019 6
2020 7
2021 16
2022 9
2023 13
2024 5
2025 8
2026 5

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168 results

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Page 1
Achondroplasia.
Horton WA, Hall JG, Hecht JT. Horton WA, et al. Among authors: hecht jt. Lancet. 2007 Jul 14;370(9582):162-172. doi: 10.1016/S0140-6736(07)61090-3. Lancet. 2007. PMID: 17630040 Review.
Sustained growth-promoting effects of vosoritide in children with achondroplasia from an ongoing phase 3 extension study.
Savarirayan R, Irving M, Wilcox WR, Bacino CA, Hoover-Fong JE, Harmatz P, Polgreen LE, Palm K, Prada CE, Kubota T, Arundel P, Kotani Y, Leiva-Gea A, Bober MB, Hecht JT, Legare JM, Lawrinson S, Low A, Sabir I, Huntsman-Labed A, Day JRS. Savarirayan R, et al. Among authors: hecht jt. Med. 2025 May 9;6(5):100566. doi: 10.1016/j.medj.2024.11.019. Epub 2024 Dec 30. Med. 2025. PMID: 39740666 Free article. Clinical Trial.
Growth in achondroplasia including stature, weight, weight-for-height and head circumference from CLARITY: achondroplasia natural history study-a multi-center retrospective cohort study of achondroplasia in the US.
Hoover-Fong JE, Schulze KJ, Alade AY, Bober MB, Gough E, Hashmi SS, Hecht JT, Legare JM, Little ME, Modaff P, Pauli RM, Rodriguez-Buritica DF, Serna ME, Smid C, Liu C, McGready J. Hoover-Fong JE, et al. Among authors: hecht jt. Orphanet J Rare Dis. 2021 Dec 23;16(1):522. doi: 10.1186/s13023-021-02141-4. Orphanet J Rare Dis. 2021. PMID: 34949201 Free PMC article.
Neurologic manifestations of achondroplasia.
Hecht JT, Bodensteiner JB, Butler IJ. Hecht JT, et al. Handb Clin Neurol. 2014;119:551-63. doi: 10.1016/B978-0-7020-4086-3.00036-9. Handb Clin Neurol. 2014. PMID: 24365319 Review.
Etiopathogenesis of equinovarus foot malformations.
Bacino CA, Hecht JT. Bacino CA, et al. Among authors: hecht jt. Eur J Med Genet. 2014 Aug;57(8):473-9. doi: 10.1016/j.ejmg.2014.06.001. Epub 2014 Jun 13. Eur J Med Genet. 2014. PMID: 24932901 Review.
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy.
Robinson K, Singh SK, Walkup RB, Fawwal DV, Vilfort KM, Koloskee A, Fashina A, Adeyemo WL, Beaty TH, Butali A, Buxó CJ, Chung WK, Cutler DJ, Epstein MP, Gasser B, Gowans LJJ, Hecht JT, Mankad A, Moreno Uribe L, Scott DA, Shaw GM, Thomas MA, Weinberg SM, Liao EC, Brand H, Marazita ML, Lipinski RJ, Murray JC, Cornell RA, Leslie-Clarkson EJ. Robinson K, et al. Among authors: hecht jt. Am J Hum Genet. 2025 Oct 2;112(10):2422-2439. doi: 10.1016/j.ajhg.2025.08.008. Epub 2025 Sep 2. Am J Hum Genet. 2025. PMID: 40902599 Free PMC article.
Pseudoachondroplasia and painful sequelae.
Gamble C, Nguyen J, Hashmi SS, Hecht JT. Gamble C, et al. Among authors: hecht jt. Am J Med Genet A. 2015 Nov;167A(11):2618-22. doi: 10.1002/ajmg.a.37253. Epub 2015 Jul 14. Am J Med Genet A. 2015. PMID: 26177939
Cartilage oligomeric matrix protein: COMPopathies and beyond.
Posey KL, Coustry F, Hecht JT. Posey KL, et al. Among authors: hecht jt. Matrix Biol. 2018 Oct;71-72:161-173. doi: 10.1016/j.matbio.2018.02.023. Epub 2018 Mar 9. Matrix Biol. 2018. PMID: 29530484 Free PMC article. Review.
Variants in CALD1, ESRP1, and RBFOX1 are associated with orofacial cleft risk.
Carlson JC, Zhang X, Erdogan-Yildirim Z, Beaty TH, Butali A, Buxó CJ, Gowans LJJ, Hecht JT, Long RE, Moreno L, Murray JC, Orioli IM, Padilla C, Wehby GL, Feingold E, Leslie-Clarkson EJ, Weinberg SM, Marazita ML, Shaffer JR. Carlson JC, et al. Among authors: hecht jt. PLoS Genet. 2025 Sep 30;21(9):e1011581. doi: 10.1371/journal.pgen.1011581. eCollection 2025 Sep. PLoS Genet. 2025. PMID: 41026798 Free PMC article.
168 results