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

Year Number of Results
1966 1
1967 1
1968 1
1970 1
1975 4
1977 2
1978 1
1979 1
1980 1
1981 5
1983 2
1984 1
1997 1
2001 1
2010 1
2011 2
2012 5
2013 5
2014 4
2015 5
2016 10
2017 11
2018 7
2019 2
2020 11
2021 7
2022 4
2023 4
2024 5
2025 5

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101 results

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Page 1
Commentary.
Peake R. Peake R. Clin Chem. 2018 Oct;64(10):1437. doi: 10.1373/clinchem.2018.288126. Clin Chem. 2018. PMID: 30266718 No abstract available.
Biallelic variants in HECT E3 paralogs, HECTD4 and UBE3C, encoding ubiquitin ligases cause neurodevelopmental disorders that overlap with Angelman syndrome.
Faqeih EA, Alghamdi MA, Almahroos MA, Alharby E, Almuntashri M, Alshangiti AM, Clément P, Calame DG, Qebibo L, Burglen L, Doco-Fenzy M, Mastrangelo M, Torella A, Manti F, Nigro V, Alban Z, Alharbi GS, Hashmi JA, Alraddadi R, Alamri R, Mitani T, Magalie B, Coban-Akdemir Z, Geckinli BB, Pehlivan D, Romito A, Karageorgou V, Martini J, Colin E, Bonneau D, Bertoli-Avella A, Lupski JR, Pastore A, Peake RWA, Dallol A, Alfadhel M, Almontashiri NAM. Faqeih EA, et al. Among authors: peake rwa. Genet Med. 2023 Feb;25(2):100323. doi: 10.1016/j.gim.2022.10.006. Epub 2022 Nov 19. Genet Med. 2023. PMID: 36401616 Free article.
Newborn Screening for Lysosomal Storage Disorders.
Peake RW, Bodamer OA. Peake RW, et al. J Pediatr Genet. 2017 Mar;6(1):51-60. doi: 10.1055/s-0036-1593843. Epub 2016 Dec 2. J Pediatr Genet. 2017. PMID: 28180027 Free PMC article. Review.
Thyroiditis.
Peake RL. Peake RL. Postgrad Med. 1975 Jun;57(7):95-8. doi: 10.1080/00325481.1975.11714076. Postgrad Med. 1975. PMID: 1173287 No abstract available.
Ancient genomics support deep divergence between Eastern and Western Mediterranean Indo-European languages.
Yediay FE, Kroonen G, Sabatini S, Frei KM, Frank AB, Pinotti T, Wigman A, Thorsø R, Vimala T, McColl H, Moutafi I, Altinkaya I, Ramsøe A, Gaunitz C, Renaud G, Martin AM, Demeter F, Scorrano G, Canci A, Fischer P, Duyar I, Serhal C, Varzari A, Türkteki M, O'Shea J, Rahmstorf L, Polat G, Atamtürk D, Vinner L, Omura S, Matsumura K, Cao J, Valeur Seersholm F, Morillo Leon JM, Voutsaki S, Orgeolet R, Burke B, Herrmann NP, Recchia G, Corazza S, Borgna E, Sampò MC, Trucco F, Pando AP, Schjellerup Jørkov ML, Courtaud P, Peake R, Bao JFG, Parditka G, Stenderup J, Sjögren KG, Staring J, Olsen L, Deyneko IV, Pálfi G, Aldana PML, Burns B, Paja L, Mühlenbock C, Cavazzuti C, Cazzella A, Lagia A, Lambrinoudakis V, Kolonas L, Rambach J, Sava E, Agulnikov S, Castañeda Fernández V, Broné M, Peña Romo V, Molina González F, Cámara Serrano JA, Jiménez Brobeil S, Nájera Molino T, Rodríguez Ariza MO, Galán Saulnier C, González Martín A, Cauwe N, Mordant C, Roscio M, Staniaszek L, Tafuri MA, Yıldırım T, Salzani L, Sand Korneliussen T, Moreno-Mayar JV, Allentoft ME, Sikora M, Nielsen R, Kristiansen K, Willerslev E. Yediay FE, et al. Among authors: peake r. bioRxiv [Preprint]. 2024 Dec 2:2024.12.02.626332. doi: 10.1101/2024.12.02.626332. bioRxiv. 2024. PMID: 39677618 Free PMC article. Preprint.
ME2 Deficiency Is Associated With Recessive Neurodevelopmental Disorder.
Almontashiri NAM, Alharby E, Saleh M, Abu-Farha M, Alasmari A, Gebbia M, Hiesl C, Peake RWA, Amr SS, Boles E, Roth FP, Abubaker J. Almontashiri NAM, et al. Among authors: peake rwa. Clin Genet. 2025 Feb;107(2):201-207. doi: 10.1111/cge.14632. Epub 2024 Oct 14. Clin Genet. 2025. PMID: 39401966
Indications for Thyroid Surgery.
Hardin WJ, McKenney JF, Peake RL, Crile G Jr, McMurry JF Jr. Hardin WJ, et al. Among authors: peake rl. Postgrad Med. 1975 Jun;57(7):121-124. doi: 10.1080/00325481.1975.11714079. Postgrad Med. 1975. PMID: 27410788 No abstract available.
101 results