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

Year Number of Results
1949 2
1952 1
1953 1
1954 1
1956 1
1957 1
1959 1
1964 1
1969 1
1970 1
1971 1
1973 1
1974 4
1975 2
1976 1
1979 4
1980 1
1981 1
1983 1
1984 1
1985 1
1986 1
1988 1
1990 2
1991 1
1995 1
1996 1
1997 1
1999 3
2002 2
2005 2
2006 4
2007 1
2008 1
2011 1
2012 1
2013 2
2014 3
2015 2
2016 2
2017 3
2018 2
2019 2
2020 8
2021 6
2022 7
2023 3
2024 2

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88 results

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Page 1
Whole-genome sequencing of patients with rare diseases in a national health system.
Turro E, Astle WJ, Megy K, Gräf S, Greene D, Shamardina O, Allen HL, Sanchis-Juan A, Frontini M, Thys C, Stephens J, Mapeta R, Burren OS, Downes K, Haimel M, Tuna S, Deevi SVV, Aitman TJ, Bennett DL, Calleja P, Carss K, Caulfield MJ, Chinnery PF, Dixon PH, Gale DP, James R, Koziell A, Laffan MA, Levine AP, Maher ER, Markus HS, Morales J, Morrell NW, Mumford AD, Ormondroyd E, Rankin S, Rendon A, Richardson S, Roberts I, Roy NBA, Saleem MA, Smith KGC, Stark H, Tan RYY, Themistocleous AC, Thrasher AJ, Watkins H, Webster AR, Wilkins MR, Williamson C, Whitworth J, Humphray S, Bentley DR; NIHR BioResource for the 100,000 Genomes Project; Kingston N, Walker N, Bradley JR, Ashford S, Penkett CJ, Freson K, Stirrups KE, Raymond FL, Ouwehand WH. Turro E, et al. Among authors: allen hl. Nature. 2020 Jul;583(7814):96-102. doi: 10.1038/s41586-020-2434-2. Epub 2020 Jun 24. Nature. 2020. PMID: 32581362 Free PMC article.
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.
Lorenzini T, Fliegauf M, Klammer N, Frede N, Proietti M, Bulashevska A, Camacho-Ordonez N, Varjosalo M, Kinnunen M, de Vries E, van der Meer JWM, Ameratunga R, Roifman CM, Schejter YD, Kobbe R, Hautala T, Atschekzei F, Schmidt RE, Schröder C, Stepensky P, Shadur B, Pedroza LA, van der Flier M, Martínez-Gallo M, Gonzalez-Granado LI, Allende LM, Shcherbina A, Kuzmenko N, Zakharova V, Neves JF, Svec P, Fischer U, Ip W, Bartsch O, Barış S, Klein C, Geha R, Chou J, Alosaimi M, Weintraub L, Boztug K, Hirschmugl T, Dos Santos Vilela MM, Holzinger D, Seidl M, Lougaris V, Plebani A, Alsina L, Piquer-Gibert M, Deyà-Martínez A, Slade CA, Aghamohammadi A, Abolhassani H, Hammarström L, Kuismin O, Helminen M, Allen HL, Thaventhiran JE, Freeman AF, Cook M, Bakhtiar S, Christiansen M, Cunningham-Rundles C, Patel NC, Rae W, Niehues T, Brauer N, Syrjänen J, Seppänen MRJ, Burns SO, Tuijnenburg P, Kuijpers TW; NIHR BioResource; Warnatz K, Grimbacher B; NIHR BioResource. Lorenzini T, et al. Among authors: allen hl. J Allergy Clin Immunol. 2020 Oct;146(4):901-911. doi: 10.1016/j.jaci.2019.11.051. Epub 2020 Apr 9. J Allergy Clin Immunol. 2020. PMID: 32278790 Free PMC article.
Medicaid's Heavy Lift.
Allen HL. Allen HL. Milbank Q. 2019 Dec;97(4):935-938. doi: 10.1111/1468-0009.12433. Epub 2019 Nov 19. Milbank Q. 2019. PMID: 31742739 Free PMC article. No abstract available.
Variants in CLDN5 cause a syndrome characterized by seizures, microcephaly and brain calcifications.
Deshwar AR, Cytrynbaum C, Murthy H, Zon J, Chitayat D, Volpatti J, Newbury-Ecob R, Ellard S, Allen HL, Yu EP, Noche R, Walker S, Scherer SW, Mahida S, Elitt CM, Nicolas G, Goldenberg A, Saugier-Veber P, Lecoquierre F, Dabaj I, Meddaugh H, Marble M, Keppler-Noreuil KM, Drayson L, Barañano KW, Chassevent A, Agre K, Létard P, Bilan F, Le Guyader G, Laquerrière A, Ramsey K, Henderson L, Brady L, Tarnopolsky M, Bainbridge M, Friedman J, Capri Y, Athayde L, Kok F, Gurgel-Giannetti J, Ramos LLP, Blaser S, Dowling JJ, Weksberg R. Deshwar AR, et al. Among authors: allen hl. Brain. 2023 Jun 1;146(6):2285-2297. doi: 10.1093/brain/awac461. Brain. 2023. PMID: 36477332
Immunodeficiency, autoimmunity, and increased risk of B cell malignancy in humans with TRAF3 mutations.
Rae W, Sowerby JM, Verhoeven D, Youssef M, Kotagiri P, Savinykh N, Coomber EL, Boneparth A, Chan A, Gong C, Jansen MH, du Long R, Santilli G, Simeoni I, Stephens J, Wu K, Zinicola M, Allen HL, Baxendale H, Kumararatne D, Gkrania-Klotsas E, Scheffler Mendoza SC, Yamazaki-Nakashimada MA, Ruiz LB, Rojas-Maruri CM, Lugo Reyes SO, Lyons PA, Williams AP, Hodson DJ, Bishop GA, Thrasher AJ, Thomas DC, Murphy MP, Vyse TJ, Milner JD, Kuijpers TW, Smith KGC. Rae W, et al. Among authors: allen hl. Sci Immunol. 2022 Aug 12;7(74):eabn3800. doi: 10.1126/sciimmunol.abn3800. Epub 2022 Aug 12. Sci Immunol. 2022. PMID: 35960817
Disparities in Mistreatment During Childbirth.
Liu C, Underhill K, Aubey JJ, Samari G, Allen HL, Daw JR. Liu C, et al. Among authors: allen hl. JAMA Netw Open. 2024 Apr 1;7(4):e244873. doi: 10.1001/jamanetworkopen.2024.4873. JAMA Netw Open. 2024. PMID: 38573636 Free article.
Can Medicaid Expansion Prevent Housing Evictions?
Allen HL, Eliason E, Zewde N, Gross T. Allen HL, et al. Health Aff (Millwood). 2019 Sep;38(9):1451-1457. doi: 10.1377/hlthaff.2018.05071. Health Aff (Millwood). 2019. PMID: 31479379
Relationship Between Personality Measures and Perceived Mental Fatigability.
Allen HL, Gmelin T, Moored KD, Boudreau RM, Smagula SF, Cohen RW, Katz R, Stone K, Cauley JA, Glynn NW; Osteoporotic Fractures in Men Study (MrOS) Research Group. Allen HL, et al. J Aging Health. 2022 Aug-Sep;34(4-5):750-760. doi: 10.1177/08982643211055032. Epub 2021 Nov 25. J Aging Health. 2022. PMID: 34821521 Free PMC article.
Feline mammary hypertrophy.
Allen HL. Allen HL. Vet Pathol. 1973;10(6):501-8. doi: 10.1177/030098587301000603. Vet Pathol. 1973. PMID: 4807748 No abstract available.
ADA2 deficiency complicated by EBV-driven lymphoproliferative disease.
Staples E, Simeoni I, Stephens JC, Allen HL; NIHR-BioResource; Wright P, Davies EG, Javid B, Gkrania-Klotsas E, Gattens M, Firth H, Shamardina O, Deevi SVV, Prapa M, Uttenthal B, Kumararatne D, Thaventhiran JED. Staples E, et al. Among authors: allen hl. Clin Immunol. 2020 Jun;215:108443. doi: 10.1016/j.clim.2020.108443. Epub 2020 Apr 27. Clin Immunol. 2020. PMID: 32353633 Free PMC article.
88 results