Multicascaded Feature Fusion-Based Deep Learning Network for Local Climate Zone Classification Based on the So2Sat LCZ42 Benchmark Dataset
Ji, Weizhen, Chen, Yunhao, Li, Kangning, Dai, Xiujuan
Published in IEEE journal of selected topics in applied earth observations and remote sensing (2023)
Published in IEEE journal of selected topics in applied earth observations and remote sensing (2023)
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Human autoinflammatory disease reveals ELF4 as a transcriptional regulator of inflammation
Tyler, Paul M., Bucklin, Molly L., Zhao, Mengting, Maher, Timothy J., Rice, Andrew J., Ji, Weizhen, Warner, Neil, Pan, Jie, Morotti, Raffaella, McCarthy, Paul, Griffiths, Anne, van Rossum, Annemarie M. C., Hollink, Iris H.I.M., Dalm, Virgil A.S.H., Catanzaro, Jason, Lakhani, Saquib A., Muise, Aleixo M., Lucas, Carrie L.
Published in Nature immunology (01.09.2021)
Published in Nature immunology (01.09.2021)
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A Retrieval Algorithm for Passive Microwave-Based Land Surface Temperature Considering Spatiotemporal Soil Moisture and Land Scenarios
Ji, Weizhen, Chen, Yunhao, Gao, Han, Xia, Haiping
Published in IEEE journal of selected topics in applied earth observations and remote sensing (2024)
Published in IEEE journal of selected topics in applied earth observations and remote sensing (2024)
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Journal Article
Corrigendum to “Adaptive multi-object tracking based on sensors fusion with confidence updating” [Inter. J. Appl. Earth Obs. Geoinform. 125 (2023) 103577]
Liu, Junting, Liu, Deer, Ji, Weizhen, Cai, Chengfeng, Liu, Zhen
Published in International journal of applied earth observation and geoinformation (01.09.2024)
Published in International journal of applied earth observation and geoinformation (01.09.2024)
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Journal Article
K⁺ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension
Choi, Murim, Scholl, Ute I, Yue, Peng, Björklund, Peyman, Zhao, Bixiao, Nelson-Williams, Carol, Ji, Weizhen, Cho, Yoonsang, Patel, Aniruddh, Men, Clara J, Lolis, Elias, Wisgerhof, Max V, Geller, David S, Mane, Shrikant, Hellman, Per, Westin, Gunnar, Åkerström, Göran, Wang, Wenhui, Carling, Tobias, Lifton, Richard P
Published in Science (American Association for the Advancement of Science) (11.02.2011)
Published in Science (American Association for the Advancement of Science) (11.02.2011)
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Journal Article
De novo damaging variants associated with congenital heart diseases contribute to the connectome
Ji, Weizhen, Ferdman, Dina, Copel, Joshua, Scheinost, Dustin, Shabanova, Veronika, Brueckner, Martina, Khokha, Mustafa K., Ment, Laura R.
Published in Scientific reports (27.04.2020)
Published in Scientific reports (27.04.2020)
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Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
Choi, Murim, Scholl, Ute I, Ji, Weizhen, Liu, Tiewen, Tikhonova, Irina R, Zumbo, Paul, Nayir, Ahmet, Bakkaloğlu, Aysin, Özen, Seza, Sanjad, Sami, Nelson-Williams, Carol, Farhi, Anita, Mane, Shrikant, Lifton, Richard P
Published in Proceedings of the National Academy of Sciences - PNAS (10.11.2009)
Published in Proceedings of the National Academy of Sciences - PNAS (10.11.2009)
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Extracting photovoltaic panels from heterogeneous remote sensing images with spatial and spectral differences
Zhao, Zhiyu, Chen, Yunhao, Li, Kangning, Ji, Weizhen, Sun, Hao
Published in IEEE journal of selected topics in applied earth observations and remote sensing (01.01.2024)
Published in IEEE journal of selected topics in applied earth observations and remote sensing (01.01.2024)
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Journal Article
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
Larson, Martin G, Ji, Weizhen, Newton-Cheh, Christopher, O'Roak, Brian J, Foo, Jia Nee, Simon, David B, Zhao, Hongyu, Levy, Daniel, Lifton, Richard P, State, Matthew W
Published in Nature genetics (01.05.2008)
Published in Nature genetics (01.05.2008)
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Journal Article
Novel compound heterozygous variants in NHLRC2 in a patient with FINCA syndrome
Brodsky, Nina N, Boyarchuk, Oksana, Kovalchuk, Tetyana, Hariyan, Tetyana, Rice, Andrew, Ji, Weizhen, Khokha, Mustafa, Lakhani, Saquib, Lucas, Carrie L
Published in Journal of human genetics (01.10.2020)
Published in Journal of human genetics (01.10.2020)
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Unraveling the genetic tapestry of pediatric sarcomeric cardiomyopathies and masquerading phenocopies in Jordan
Azab, Bilal, Aburizeg, Dunia, Shaaban, Sherin T., Ji, Weizhen, Mustafa, Lina, Isbeih, Nooredeen Jamal, Al-Akily, Amal Saleh, Mohammad, Hashim, Jeffries, Lauren, Khokha, Mustafa, Lakhani, Saquib A., Al-Ammouri, Iyad
Published in Scientific reports (02.07.2024)
Published in Scientific reports (02.07.2024)
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Journal Article
DYNC1H1‐related disorders: A description of four new unrelated patients and a comprehensive review of previously reported variants
Amabile, Sonia, Jeffries, Lauren, McGrath, James M., Ji, Weizhen, Spencer‐Manzon, Michele, Zhang, Hui, Lakhani, Saquib A.
Published in American journal of medical genetics. Part A (01.09.2020)
Published in American journal of medical genetics. Part A (01.09.2020)
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Journal Article
De novo pathogenic variants in neuronal differentiation factor 2 (NEUROD2) cause a form of early infantile epileptic encephalopathy
Sega, Annalisa G, Mis, Emily K, Lindstrom, Kristin, Mercimek-Andrews, Saadet, Ji, Weizhen, Cho, Megan T, Juusola, Jane, Konstantino, Monica, Jeffries, Lauren, Khokha, Mustafa K, Lakhani, Saquib Ali
Published in Journal of medical genetics (01.02.2019)
Published in Journal of medical genetics (01.02.2019)
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Journal Article
Uncontrolled Epstein-Barr Virus as an Atypical Presentation of Deficiency in ADA2 (DADA2)
Brooks, Joel P., Rice, Andrew J., Ji, Weizhen, Lanahan, Stephen M., Konstantino, Monica, Dara, Jasmeen, Hershfield, Michael S., Cruickshank, Amy, Dokmeci, Elif, Lakhani, Saquib, Lucas, Carrie L.
Published in Journal of clinical immunology (01.04.2021)
Published in Journal of clinical immunology (01.04.2021)
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Journal Article
SMC5 Plays Independent Roles in Congenital Heart Disease and Neurodevelopmental Disability
O'Brien, Matthew P, Pryzhkova, Marina V, Lake, Evelyn M R, Mandino, Francesca, Shen, Xilin, Karnik, Ruchika, Atkins, Alisa, Xu, Michelle J, Ji, Weizhen, Konstantino, Monica, Brueckner, Martina, Ment, Laura R, Khokha, Mustafa K, Jordan, Philip W
Published in International journal of molecular sciences (28.12.2023)
Published in International journal of molecular sciences (28.12.2023)
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Journal Article
A novel SAMD9 mutation causing MIRAGE syndrome: An expansion and review of phenotype, dysmorphology, and natural history
Jeffries, Lauren, Shima, Hirohito, Ji, Weizhen, Panisello‐Manterola, David, McGrath, James, Bird, Lynne M., Konstantino, Monica, Narumi, Satoshi, Lakhani, Saquib
Published in American journal of medical genetics. Part A (01.02.2018)
Published in American journal of medical genetics. Part A (01.02.2018)
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