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

Year Number of Results
2007 1
2008 1
2013 2
2014 6
2015 6
2016 2
2017 2
2018 4
2019 3
2020 6
2021 9
2022 8
2023 2
2024 2
2025 0

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41 results

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Page 1
Imaging in osteopetrosis.
Calder AD, Arulkumaran S, D'Arco F. Calder AD, et al. Bone. 2022 Dec;165:116560. doi: 10.1016/j.bone.2022.116560. Epub 2022 Sep 15. Bone. 2022. PMID: 36116759 Review.
Achondroplasia: Really rhizomelic?
Shelmerdine SC, Brittain H, Arthurs OJ, Calder AD. Shelmerdine SC, et al. Among authors: calder ad. Am J Med Genet A. 2016 Aug;170(8):2039-43. doi: 10.1002/ajmg.a.37776. Epub 2016 Jun 3. Am J Med Genet A. 2016. PMID: 27257098
Lung infections in immunocompromised children.
Calder AD, Perucca G, Johnson SM, Pandey AR, Moshal K, Kusters MA. Calder AD, et al. Pediatr Radiol. 2024 Apr;54(4):530-547. doi: 10.1007/s00247-023-05735-1. Epub 2023 Aug 17. Pediatr Radiol. 2024. PMID: 37589764 Review.
Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability.
Zhang C, Jolly A, Shayota BJ, Mazzeu JF, Du H, Dawood M, Soper PC, Ramalho de Lima A, Ferreira BM, Coban-Akdemir Z, White J, Shears D, Thomson FR, Douglas SL, Wainwright A, Bailey K, Wordsworth P, Oldridge M, Lester T, Calder AD, Dumic K, Banka S, Donnai D, Jhangiani SN, Potocki L, Chung WK, Mora S, Northrup H, Ashfaq M, Rosenfeld JA, Mason K, Pollack LC, McConkie-Rosell A, Kelly W, McDonald M, Hauser NS, Leahy P, Powell CM, Boy R, Honjo RS, Kok F, Martelli LR, Filho VO, Genomics England Research Consortium, Muzny DM, Gibbs RA, Posey JE, Liu P, Lupski JR, Sutton VR, Carvalho CMB. Zhang C, et al. Among authors: calder ad. HGG Adv. 2021 Dec 3;3(1):100074. doi: 10.1016/j.xhgg.2021.100074. eCollection 2022 Jan 13. HGG Adv. 2021. PMID: 35047859 Free PMC article.
Sedaghatian spondylometaphyseal dysplasia in two siblings.
Peshimam N, Farah H, Caswell R, Ellard S, Jan W, Calder AD, Cobben J, Kariholu U, Leitch HG. Peshimam N, et al. Among authors: calder ad. Eur J Med Genet. 2022 Aug;65(8):104541. doi: 10.1016/j.ejmg.2022.104541. Epub 2022 Jun 16. Eur J Med Genet. 2022. PMID: 35718083 Free article.
The changing world of skeletal dysplasia.
Calder AD. Calder AD. Lancet Child Adolesc Health. 2020 Apr;4(4):253-254. doi: 10.1016/S2352-4642(20)30056-0. Epub 2020 Feb 28. Lancet Child Adolesc Health. 2020. PMID: 32119838 No abstract available.
Variable skeletal phenotypes associated with biallelic variants in PRKG2.
Pagnamenta AT, Diaz-Gonzalez F, Banos-Pinero B, Ferla MP, Toosi MB, Calder AD, Karimiani EG, Doosti M, Wainwright A, Wordsworth P, Bailey K, Ejeskär K, Lester T, Maroofian R, Heath KE, Tajsharghi H, Shears D, Taylor JC; Genomics England Research Consortium. Pagnamenta AT, et al. Among authors: calder ad. J Med Genet. 2022 Oct;59(10):947-950. doi: 10.1136/jmedgenet-2021-108027. Epub 2021 Nov 15. J Med Genet. 2022. PMID: 34782440 Free PMC article. No abstract available.
41 results