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

Year Number of Results
1968 1
2007 1
2008 1
2009 2
2010 5
2011 3
2012 3
2013 2
2014 1
2015 5
2016 7
2017 2
2018 1
2019 2
2020 5
2021 3
2022 1
2024 1
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2026 0

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40 results

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Page 1
The long and short of the S-locus in Turnera (Passifloraceae).
Shore JS, Hamam HJ, Chafe PDJ, Labonne JDJ, Henning PM, McCubbin AG. Shore JS, et al. Among authors: labonne jdj. New Phytol. 2019 Nov;224(3):1316-1329. doi: 10.1111/nph.15970. Epub 2019 Jul 15. New Phytol. 2019. PMID: 31144315 Free article.
StoichLife: A Global Dataset of Plant and Animal Elemental Content.
González AL, Merder J, Andraczek K, Brose U, Filipiak M, Harpole WS, Hillebrand H, Jackson MC, Jochum M, Leroux SJ, Nessel MP, Onstein RE, Paseka R, Perry GLW, Rugenski A, Sitters J, Sperfeld E, Striebel M, Zandona E, Aymes JC, Blanckaert A, Bluhm SL, Doi H, Eisenhauer N, Farjalla VF, Hood J, Kratina P, Labonne J, Lovelock CE, Moody EK, Mozsár A, Nash L, Pollierer MM, Potapov A, Romero GQ, Roussel JM, Scheu S, Scheunemann N, Seeber J, Steinwandter M, Susanti WI, Tiunov A, Dézerald O. González AL, et al. Among authors: labonne j. Sci Data. 2025 Apr 3;12(1):569. doi: 10.1038/s41597-025-04852-w. Sci Data. 2025. PMID: 40180992 Free PMC article.
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families.
Doll J, Vona B, Schnapp L, Rüschendorf F, Khan I, Khan S, Muhammad N, Alam Khan S, Nawaz H, Khan A, Ahmad N, Kolb SM, Kühlewein L, Labonne JDJ, Layman LC, Hofrichter MAH, Röder T, Dittrich M, Müller T, Graves TD, Kong IK, Nanda I, Kim HG, Haaf T. Doll J, et al. Among authors: labonne jdj. Genes (Basel). 2020 Nov 11;11(11):1329. doi: 10.3390/genes11111329. Genes (Basel). 2020. PMID: 33187236 Free PMC article.
Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3).
Susgun S, Ben-Mahmoud A, Rüschendorf F, Ku B, Hussain SI, Schulz S, Puk O, Biskup S, Labonne JDJ, Don DW, Gupta V, Choi TI, Khan S, Wasif N, Lacassie Y, Layman LC, Ugur Iseri SA, Kim CH, Kim HG. Susgun S, et al. Among authors: labonne jdj. Hum Mutat. 2024 Jan 5;2024:5518289. doi: 10.1155/2024/5518289. eCollection 2024. Hum Mutat. 2024. PMID: 40225942 Free PMC article.
Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism.
Kim HG, Rosenfeld JA, Scott DA, Bénédicte G, Labonne JD, Brown J, McGuire M, Mahida S, Naidu S, Gutierrez J, Lesca G, des Portes V, Bruel AL, Sorlin A, Xia F, Capri Y, Muller E, McKnight D, Torti E, Rüschendorf F, Hummel O, Islam Z, Kolatkar PR, Layman LC, Ryu D, Kong IK, Madan-Khetarpal S, Kim CH. Kim HG, et al. Among authors: labonne jd. Mol Autism. 2019 Oct 22;10:35. doi: 10.1186/s13229-019-0286-0. eCollection 2019. Mol Autism. 2019. PMID: 31649809 Free PMC article.
40 results