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

Year Number of Results
1993 1
1994 1
1996 1
1997 5
1998 1
2000 2
2001 3
2002 3
2003 2
2004 5
2005 5
2006 7
2007 7
2008 2
2009 7
2010 8
2011 7
2012 10
2013 4
2014 1
2015 6
2016 5
2017 5
2018 5
2019 6
2020 7
2021 6
2022 6
2023 4
2024 4
2025 3
2026 1

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119 results

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Page 1
Revisiting a Rare Anomaly Described 25 Years Ago in the AJNR: A Journey from Pediatric Hemifacial Microsomia and Middle Cranial Fossa Aplasia to CSF-Lymphatic Fistula and Spontaneous Intracranial Hypotension as an Adult.
Callen AL, Khanwalkar AR, Cunningham ML, Pisani Petrucci SL, Bhaumik D, Wilhour D, Trivedi P, Lennarson P, Zander DA. Callen AL, et al. Among authors: cunningham ml. AJNR Am J Neuroradiol. 2025 Oct 1;46(10):2208-2213. doi: 10.3174/ajnr.A8760. AJNR Am J Neuroradiol. 2025. PMID: 40147836
AXIN1 mutations in nonsyndromic craniosynostosis.
Timberlake AT, Hemal K, Gustafson JA, Hao LT, Valenzuela I, Slavotinek A, Cunningham ML, Kahle KT, Lifton RP, Persing JA. Timberlake AT, et al. Among authors: cunningham ml. J Neurosurg Pediatr. 2024 Jun 21;34(3):246-251. doi: 10.3171/2024.5.PEDS24115. Print 2024 Sep 1. J Neurosurg Pediatr. 2024. PMID: 38905707 Free PMC article.
Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428.
Musolf AM, Justice CM, Erdogan-Yildirim Z, Goovaerts S, Cuellar A, Shaffer JR, Marazita ML, Claes P, Weinberg SM, Li J, Senders C, Zwienenberg M, Simeonov E, Kaneva R, Roscioli T, Di Pietro L, Barba M, Lattanzi W, Cunningham ML, Romitti PA, Boyadjiev SA. Musolf AM, et al. Among authors: cunningham ml. Sci Rep. 2024 Apr 12;14(1):8533. doi: 10.1038/s41598-024-58343-w. Sci Rep. 2024. PMID: 38609424 Free PMC article.
Expansion of the sagittal suture induces proliferation of skeletal stem cells and sustains endogenous calvarial bone regeneration.
Aldawood ZA, Mancinelli L, Geng X, Yeh SA, Di Carlo R, C Leite T, Gustafson J, Wilk K, Yozgatian J, Garakani S, Bassir SH, Cunningham ML, Lin CP, Intini G. Aldawood ZA, et al. Among authors: cunningham ml. Proc Natl Acad Sci U S A. 2023 Apr 18;120(16):e2120826120. doi: 10.1073/pnas.2120826120. Epub 2023 Apr 11. Proc Natl Acad Sci U S A. 2023. PMID: 37040407 Free PMC article.
Damaging variants in FOXI3 cause microtia and craniofacial microsomia.
Quiat D, Timberlake AT, Curran JJ, Cunningham ML, McDonough B, Artunduaga MA, DePalma SR, Duenas-Roque MM, Gorham JM, Gustafson JA, Hamdan U, Hing AV, Hurtado-Villa P, Nicolau Y, Osorno G, Pachajoa H, Porras-Hurtado GL, Quintanilla-Dieck L, Serrano L, Tumblin M, Zarante I, Luquetti DV, Eavey RD, Heike CL, Seidman JG, Seidman CE. Quiat D, et al. Among authors: cunningham ml. Genet Med. 2023 Jan;25(1):143-150. doi: 10.1016/j.gim.2022.09.005. Epub 2022 Oct 19. Genet Med. 2023. PMID: 36260083 Free PMC article.
119 results