SHINYA YAMAMOTO to Humans
This is a "connection" page, showing publications SHINYA YAMAMOTO has written about Humans.
Connection Strength
0.948
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Hippo signaling regulates cuticle pigmentation and dopamine metabolism in Drosophila. PLoS Genet. 2026 Aug; 22(8):e1012260.
Score: 0.026
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Sphingolipid and glycerophospholipid profiling in post-acute sequelae of SARS-CoV-2 infection. Sci Rep. 2026 May 10; 16(1).
Score: 0.026
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Retreatment or prolonged antiviral therapy in severe acute respiratory syndrome Coronavirus-2 infection among immunocompromised patients during 2022-2023: A nationwide claims-based cohort study in Japan. J Infect Chemother. 2025 Nov; 31(11):102830.
Score: 0.025
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Functional assays in Drosophila facilitate classification of variants of uncertain significance associated with rare diseases. Genome Res. 2025 07 01; 35(7):1473-1484.
Score: 0.024
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Collective Acoustics in Pan: Conserved Roots in the Evolution of Human Musicality. Am J Primatol. 2025 06; 87(6):e70048.
Score: 0.024
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Functional analysis of pathogenic variants in LAMB1-related leukoencephalopathy reveals genotype-phenotype correlations and suggests its role in glial cells. Hum Mol Genet. 2025 05 17; 34(11):990-999.
Score: 0.024
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Clinical impact of the use of chronic suppressive antibiotics against recurrent ventricular assist device infections. Microbiol Spectr. 2024 11 05; 12(11):e0039824.
Score: 0.023
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Exogenous oxytocin increases gaze to humans in male cats. Sci Rep. 2024 04 18; 14(1):8953.
Score: 0.022
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A report of stillbirth and subsequent maternal cannibalism observed in a free-ranging group of Japanese macaques at Awajishima, Japan. Primates. 2023 Nov; 64(6):573-578.
Score: 0.021
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Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans. Nat Rev Genet. 2024 Jan; 25(1):46-60.
Score: 0.021
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Severe TAFRO Syndrome Mimicking Hepatorenal Syndrome Successfully Treated with a Multidisciplinary Approach: A Case Report and Literature Review. Intern Med. 2023 Sep 15; 62(18):2715-2724.
Score: 0.021
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Role of Drosophila in Human Disease Research 2.0. Int J Mol Sci. 2022 Apr 11; 23(8).
Score: 0.019
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ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research. Hum Mutat. 2022 06; 43(6):743-759.
Score: 0.019
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Functional Studies of Genetic Variants Associated with Human Diseases in Notch Signaling-Related Genes Using Drosophila. Methods Mol Biol. 2022; 2472:235-276.
Score: 0.019
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A Novel Pathological Mechanism of Tertiary Lymphoid Structure Formation in the Renal Pelvis. J Am Soc Nephrol. 2022 01; 33(1):4-6.
Score: 0.019
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The fruit fly at the interface of diagnosis and pathogenic mechanisms of rare and common human diseases. Hum Mol Genet. 2019 11 21; 28(R2):R207-R214.
Score: 0.016
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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila. J Vis Exp. 2019 08 20; (150).
Score: 0.016
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Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information. J Vis Exp. 2019 08 15; (150).
Score: 0.016
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Integration of Drosophila and Human Genetics to Understand Notch Signaling Related Diseases. Adv Exp Med Biol. 2018; 1066:141-185.
Score: 0.014
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Morgan's legacy: fruit flies and the functional annotation of conserved genes. Cell. 2015 Sep 24; 163(1):12-4.
Score: 0.012
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A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases. Cell. 2014 Sep 25; 159(1):200-214.
Score: 0.012
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Dopamine dynamics and signaling in Drosophila: an overview of genes, drugs and behavioral paradigms. Exp Anim. 2014; 63(2):107-19.
Score: 0.011
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Introduction to Notch signaling. Methods Mol Biol. 2014; 1187:1-14.
Score: 0.011
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Preface. Notch signaling. Methods Mol Biol. 2014; 1187:v.
Score: 0.011
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A mutation in EGF repeat-8 of Notch discriminates between Serrate/Jagged and Delta family ligands. Science. 2012 Nov 30; 338(6111):1229-32.
Score: 0.010
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Endocytosis and intracellular trafficking of Notch and its ligands. Curr Top Dev Biol. 2010; 92:165-200.
Score: 0.008
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Significance of Nontuberculous Mycobacteria Detection in Liver Transplant Recipients: A Descriptive Epidemiology. Transplant Proc. 2026 Oct; 58(8):1557-1561.
Score: 0.007
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Uncovering phenotypic expansion in AXIN2-related disorders through precision animal modeling. Genet Med. 2026 Sep; 28(9):102648.
Score: 0.007
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Translating multi-omics into healthcare: requisites for scalable and equitable implementation. Hum Genomics. 2026 Mar 25; 20(1).
Score: 0.006
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Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorder. Genet Med. 2026 04; 28(4):101685.
Score: 0.006
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A case of chronic Campylobacter fetus infection-related glomerulonephritis, mimicking systemic autoimmune diseases. CEN Case Rep. 2026 01 13; 15(1):18.
Score: 0.006
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Resolving SLC6A1 variable expressivity with deep clinical phenotyping and Drosophila models. HGG Adv. 2026 Jan 15; 7(1):100541.
Score: 0.006
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Daptomycin resistance of Corynebacterium jeikeium due to pgsA gene mutation acquired during daptomycin treatment in a patient with infective endocarditis. Int J Infect Dis. 2025 Dec; 161:108112.
Score: 0.006
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Asian elephants (Elephas maximus) recognise human visual attention from body and face orientation. Sci Rep. 2025 Oct 02; 15(1):32623.
Score: 0.006
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Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function. Elife. 2025 Aug 27; 13.
Score: 0.006
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De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome. Brain. 2025 Aug 01; 148(8):2658-2670.
Score: 0.006
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A Rare Case of Eosinophilic Granulomatosis with Polyangiitis Following Development of Central Diabetes Insipidus: A Case Report and Literature Review. Intern Med. 2026 Jan 01; 65(1):149-155.
Score: 0.006
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Emotional contagion of fear and joy from humans to horses using a combination of facial and vocal cues. Sci Rep. 2025 May 21; 15(1):17689.
Score: 0.006
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Distinct systemic impacts of A?42 and Tau revealed by whole-organism snRNA-seq. Neuron. 2025 Jul 09; 113(13):2065-2082.e8.
Score: 0.006
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C-terminal frameshift variants in GPKOW are associated with a multisystemic X-linked disorder. Genet Med. 2025 07; 27(7):101429.
Score: 0.006
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Glucose uptake in pigment glia suppresses Tau-induced inflammation and photoreceptor degeneration. Dis Model Mech. 2025 04 01; 18(4).
Score: 0.006
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Population pharmacokinetic analysis of bevacizumab in Japanese cancer patients with proteinuria: a prospective cohort study. Cancer Chemother Pharmacol. 2025 Mar 21; 95(1):46.
Score: 0.006
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De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms. Am J Hum Genet. 2025 04 03; 112(4):846-862.
Score: 0.006
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Aligning cellular and molecular components in age-dependent tertiary lymphoid tissues of kidney and liver. PLoS One. 2025; 20(2):e0311193.
Score: 0.006
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Membranoproliferative Glomerulonephritis with Striated Ultrastructural Deposits with Significantly Elevated Fibrinogen and Fibronectin on Mass Spectrometry Analysis: A Case Report and Literature Review. Nephron. 2025; 149(7):411-421.
Score: 0.006
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Prognostic significance of body mass index in patients with metastatic renal cell carcinoma receiving first-line therapies. Urol Oncol. 2025 04; 43(4):269.e1-269.e6.
Score: 0.006
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Dysbiosis of gut microbiota in COVID-19 is associated with intestinal DNA phage dynamics of lysogenic and lytic infection. Microbiol Spectr. 2025 01 07; 13(1):e0099824.
Score: 0.006
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ATP dynamics as a predictor of future podocyte structure and function after acute ischemic kidney injury in female mice. Nat Commun. 2024 11 22; 15(1):9977.
Score: 0.006
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A Case of IgG4-Related Disease Manifesting as Extensive Abdominal Periarteritis and Membranous Nephropathy, Successfully Controlled with Low-Dose Steroid Therapy without Relapse or Complications. Nephron. 2025; 149(4):213-221.
Score: 0.006
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Characteristics of Successful Percutaneous Transluminal Renal Angioplasty Cases with Severely Impaired Kidney Function Caused by Bilateral Atherosclerotic Stenosis: A Case Series. Nephron. 2025; 149(3):160-165.
Score: 0.006
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Radiation Nephropathy Complicated by Tubulointerstitial Nephritis with Predominantly Lymphocyte and Plasma Cell Infiltration. Intern Med. 2025 Jun 01; 64(11):1696-1705.
Score: 0.006
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Pathogenic SATB2 missense variants affecting p.Gly392 have variable functional implications and result in diverse clinical phenotypes. J Med Genet. 2024 10 23; 61(11):1062-1067.
Score: 0.006
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Multi-scale hierarchical brain regions detect individual and interspecies variations of structural connectivity in macaque monkeys and humans. Neuroimage. 2024 11 15; 302:120901.
Score: 0.006
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Association between Proton Pump Inhibitors, Immune Checkpoint Inhibitors, and Acute Kidney Injury: A Nested Case-Control Study. Kidney360. 2024 09 01; 5(9):1262-1269.
Score: 0.006
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Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly. Genet Med. 2024 11; 26(11):101218.
Score: 0.006
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Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities. Genet Med. 2024 09; 26(9):101174.
Score: 0.006
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De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features. Am J Hum Genet. 2024 04 04; 111(4):742-760.
Score: 0.006
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Low serum concentrations of bevacizumab and nivolumab owing to excessive urinary loss in patients with proteinuria: a case series. Cancer Chemother Pharmacol. 2024 10; 94(4):615-622.
Score: 0.006
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Comparative exploration of mammalian deafness gene homologues in the Drosophila auditory organ shows genetic correlation between insect and vertebrate hearing. PLoS One. 2024; 19(2):e0297846.
Score: 0.006
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Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability. Proc Natl Acad Sci U S A. 2024 Feb 27; 121(9):e2322582121.
Score: 0.006
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Proteinuria frequency and subsequent renal dysfunction in bevacizumab-treated patients: a single center, retrospective, observational study. Int J Clin Oncol. 2024 Apr; 29(4):398-406.
Score: 0.006
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Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays. Elife. 2023 12 11; 12.
Score: 0.005
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Airway surveillance and lung viral control by memory T cells induced by COVID-19 mRNA vaccine. JCI Insight. 2023 11 22; 8(22).
Score: 0.005
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CpG ODN enhances the efficacy of F protein vaccine against respiratory syncytial virus infection in the upper respiratory tract via CD4+ T cells. Biochem Biophys Res Commun. 2023 12 17; 686:149143.
Score: 0.005
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Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies. Am J Hum Genet. 2023 11 02; 110(11):1919-1937.
Score: 0.005
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A Rare Case of Drug Reaction with Eosinophilia and Systemic Symptoms Syndrome Leading to Hemodialysis and Multiple Infections: A Case Report and Literature Review. Intern Med. 2024 Apr 15; 63(8):1131-1138.
Score: 0.005
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A de novo missense variant in EZH1 associated with developmental delay exhibits functional deficits in Drosophila melanogaster. Genetics. 2023 08 09; 224(4).
Score: 0.005
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A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins. Cell Rep. 2023 08 29; 42(8):112842.
Score: 0.005
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Research article antibody induction and immune response in nasal cavity by third dose of SARS-CoV-2 mRNA vaccination. Virol J. 2023 07 13; 20(1):146.
Score: 0.005
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Exploring the mechanism of BK polyomavirus-associated nephropathy through consensus gene network approach. PLoS One. 2023; 18(6):e0282534.
Score: 0.005
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Bi-allelic variants in INTS11 are associated with a complex neurological disorder. Am J Hum Genet. 2023 05 04; 110(5):774-789.
Score: 0.005
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Exploring relationships between autistic traits and body temperature, circadian rhythms, and age. Sci Rep. 2023 04 11; 13(1):5888.
Score: 0.005
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De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features. Genet Med. 2023 06; 25(6):100833.
Score: 0.005
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A Rare Case of Blindness Caused by Syphilis with Malignant Hypertensive Nephropathy. Intern Med. 2023 Nov 01; 62(21):3195-3201.
Score: 0.005
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Efficacy of antivirals and bivalent mRNA vaccines against SARS-CoV-2 isolate CH.1.1. Lancet Infect Dis. 2023 05; 23(5):525-526.
Score: 0.005
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Antiviral and bivalent vaccine efficacy against an omicron XBB.1.5 isolate. Lancet Infect Dis. 2023 04; 23(4):402-403.
Score: 0.005
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Focal Segmental Sclerosis Associated with the Novel Multi-tyrosine Kinase Inhibitor Ponatinib. Intern Med. 2023 Sep 15; 62(18):2693-2698.
Score: 0.005
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Humoral immune evasion of the omicron subvariants BQ.1.1 and XBB. Lancet Infect Dis. 2023 01; 23(1):30-32.
Score: 0.005
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Immunological Correlates of Prevention of the Onset of Seasonal H3N2 Influenza. J Infect Dis. 2022 11 11; 226(10):1800-1808.
Score: 0.005
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A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder. HGG Adv. 2023 01 12; 4(1):100157.
Score: 0.005
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The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder. Hum Mol Genet. 2022 08 25; 31(17):2934-2950.
Score: 0.005
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Horses form cross-modal representations of adults and children. Anim Cogn. 2023 Mar; 26(2):369-377.
Score: 0.005
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Characterization of the SARS-CoV-2 B.1.621 (Mu) variant. Sci Transl Med. 2022 08 10; 14(657):eabm4908.
Score: 0.005
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[Correction of Partial Volume Effect Using CT Images in Brain 18F-FDG PET]. Nihon Hoshasen Gijutsu Gakkai Zasshi. 2022 Jul 20; 78(7):741-749.
Score: 0.005
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De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies. Brain. 2022 06 03; 145(5):1684-1697.
Score: 0.005
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Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases. Cell Rep. 2022 03 15; 38(11):110517.
Score: 0.005
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A rare case of atypical ANCA-associated vasculitis without crescents overlapping with invasive pulmonary aspergillosis, successfully treated to remission with intravenous immunoglobulin therapy. CEN Case Rep. 2022 11; 11(4):428-435.
Score: 0.005
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Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling. Sci Adv. 2022 01 21; 8(3):eabl5613.
Score: 0.005
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TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila. Am J Hum Genet. 2021 09 02; 108(9):1669-1691.
Score: 0.005
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Characterization of a new SARS-CoV-2 variant that emerged in Brazil. Proc Natl Acad Sci U S A. 2021 07 06; 118(27).
Score: 0.005
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Rare deleterious de novo missense variants in Rnf2/Ring2 are associated with a neurodevelopmental disorder with unique clinical features. Hum Mol Genet. 2021 06 26; 30(14):1283-1292.
Score: 0.005
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Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11. Genet Med. 2021 10; 23(10):1889-1900.
Score: 0.005
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Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision. Orphanet J Rare Dis. 2021 05 07; 16(1):206.
Score: 0.005
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Tumor B7-H3 expression in diagnostic biopsy specimens and survival in patients with metastatic prostate cancer. Prostate Cancer Prostatic Dis. 2021 09; 24(3):767-774.
Score: 0.004
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Environment-based object values learned by local network in the striatum tail. Proc Natl Acad Sci U S A. 2021 01 26; 118(4).
Score: 0.004
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Aldehyde Dehydrogenase 1-related Genes in Triple-negative Breast Cancer Investigated Using Network Analysis. Anticancer Res. 2020 Dec; 40(12):6733-6742.
Score: 0.004
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BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms. Am J Hum Genet. 2020 12 03; 107(6):1096-1112.
Score: 0.004
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De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment. Hum Mol Genet. 2020 06 03; 29(9):1568-1579.
Score: 0.004
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De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy. Am J Hum Genet. 2020 05 07; 106(5):717-725.
Score: 0.004
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Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms. Neuron. 2020 05 20; 106(4):589-606.e6.
Score: 0.004
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A Genetic Screen for Genes That Impact Peroxisomes in Drosophila Identifies Candidate Genes for Human Disease. G3 (Bethesda). 2020 01 07; 10(1):69-77.
Score: 0.004
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Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders. Nat Commun. 2019 10 15; 10(1):4679.
Score: 0.004
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Using MARRVEL v1.2 for Bioinformatics Analysis of Human Genes and Variant Pathogenicity. Curr Protoc Bioinformatics. 2019 09; 67(1):e85.
Score: 0.004
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De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. Am J Hum Genet. 2019 08 01; 105(2):413-424.
Score: 0.004
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Myofibroblasts acquire retinoic acid-producing ability during fibroblast-to-myofibroblast transition?following kidney injury. Kidney Int. 2019 03; 95(3):526-539.
Score: 0.004
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Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease. N Engl J Med. 2018 11 29; 379(22):2131-2139.
Score: 0.004
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Preliminary Kidney Parenchymal Ligation Using Endoloop Ligatures-A Simple Method to Achieve a Trifecta in Laparoscopic Partial Nephrectomy Without Hilar Clamping for Polar Complex Tumors. Urology. 2018 11; 121:182-188.
Score: 0.004
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Rapid and Integrative Discovery of Retina Regulatory Molecules. Cell Rep. 2018 08 28; 24(9):2506-2519.
Score: 0.004
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Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder. Hum Mol Genet. 2018 07 15; 27(14):2454-2465.
Score: 0.004
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Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder. Am J Hum Genet. 2018 03 01; 102(3):494-504.
Score: 0.004
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Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research. Genetics. 2017 09; 207(1):9-27.
Score: 0.004
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Clinically severe CACNA1A alleles affect synaptic function and neurodegeneration differentially. PLoS Genet. 2017 Jul; 13(7):e1006905.
Score: 0.004
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MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome. Am J Hum Genet. 2017 Jun 01; 100(6):843-853.
Score: 0.003
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A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3. Am J Hum Genet. 2017 Jan 05; 100(1):128-137.
Score: 0.003
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Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease. PLoS Genet. 2016 Oct; 12(10):e1006327.
Score: 0.003
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Fruit flies in biomedical research. Genetics. 2015 Mar; 199(3):639-53.
Score: 0.003
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Intraoperative red cell salvage during obstetric surgery in 50 Japanese women. Int J Gynaecol Obstet. 2015 Mar; 128(3):256-9.
Score: 0.003
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Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production. Elife. 2014 Oct 14; 3.
Score: 0.003
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Shared mechanisms between Drosophila peripheral nervous system development and human neurodegenerative diseases. Curr Opin Neurobiol. 2014 Aug; 27:158-64.
Score: 0.003
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Why skill matters. Trends Cogn Sci. 2013 Sep; 17(9):434-41.
Score: 0.003
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The C8ORF38 homologue Sicily is a cytosolic chaperone for a mitochondrial complex I subunit. J Cell Biol. 2013 Mar 18; 200(6):807-20.
Score: 0.003