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1586 citation(s) found for "Xu, Wei".

RefAI: a GPT-powered retrieval-augmented generative tool for biomedical literature recommendation and summarization
Li, Yiming , Zhao, Jeff, Li, Manqi , Dang, Yifang , Li, Jianfu , Sun, Zenan , Hussein, Usama, Wen, Jianguo, Li, Shenduo , Hu, Xinyue , Yang, Daowei, Feng, Jingna , Li, Zehan , He, Jianping , Tao, Wei , Lou, Yanyan , Sun, Zenan , Abdelhameed, Ahmed M, Duan, Tiehang , Li, Fang , Tao, Cui , Dang, Yifang , Li, Yiming , Yu, Evan Y , Wen, Jianguo, Abdelhameed, Ahmed , Mai, Junhua , Yu, Yue , Li, Fang , Tao, Cui

Journal of the American Medical Informatics Association | May 21, 2024 | Volume: 31 | Issue: 9 | Pages: 2030-2039

10.1093/jamia/ocae129 | PMID 38857454 Get It

Abstract Objectives Precise literature recommendation and summarization are crucial for biomedical professionals. While the latest iteration of generative pretrained transformer (GPT) incorporates 2 distinct modes—real-time search and pretrained model utilization—it encounters challenges in dealing with these tasks. Specifically, the real-time search can pinpoint some relevant articles but occasionally provides fabricated papers, whereas the pretrained model excels in generating well-structured summaries but struggles to cite specific sources. In response, this study introduces RefAI, an innovative retrieval-augmented generative tool designed to synergize the strengths of large language models (LLMs) while overcoming their limitations. Materials and Methods RefAI utilized PubMed for systematic literature retrieval, employed a novel multivariable algorithm for article recommendation, and leveraged GPT-4 turbo for summarization. Ten queries under 2 prevalent topics (“cancer immunotherapy and target therapy” and “LLMs in medicine”) were chosen as use cases and 3 established counterparts (ChatGPT-4, ScholarAI, and Gemini) as our baselines. The evaluation was conducted by 10 domain experts through standard statistical analyses for performance comparison. Results The overall performance of RefAI surpassed that of the baselines across 5 evaluated dimensions—relevance and quality for literature recommendation, accuracy, comprehensiveness, and reference integration for summarization, with the majority exhibiting statistically significant improvements (P-values <.05). Discussion RefAI demonstrated substantial improvements in literature recommendation and summarization over existing tools, addressing issues like fabricated papers, metadata inaccuracies, restricted recommendations, and poor reference integration. Conclusion By augmenting LLM with external resources and a novel ranking algorithm, RefAI is uniquely capable of recommending high-quality literature and generating well-structured summaries, holding the potential to meet the critical needs of biomedical professionals in navigating and synthesizing vast amounts of scientific literature.
Histopathology Findings and Outcomes of Non-Nephrotic Range Proteinuria in Adults and Children
Itoku, Ai, Bu, Lihong , Hao, Wei , Kaskel, Rick , Pullman, James , Reidy, Kimberly J.

Journal of the American Society of Nephrology | May 17, 2024 | Volume: 34 | Issue: 11S | Pages: 252-252

10.1681/asn.20233411s1252c Get It

Time-Restricted Feeding and Autosomal Dominant Polycystic Kidney Disease: A Pilot, Randomized Clinical Trial
Coleman, Erin R., George, Diana, Farmer‐Bailey, Heather, Ramanathan, Sumana, Gregory, Adriana , Chonchol, Michel , Thomas, Elizabeth A. , Kline, Timothy L. , Steele, Cortney , Wang, Wei , Gitomer, Berenice Y , Thomas, Elizabeth, Nowak, Kristen L.

Journal of the American Society of Nephrology | May 17, 2024 | Volume: 34 | Issue: 11S | Pages: 206-206

10.1681/asn.20233411s1206c Get It

Systemic Inflammation and Kidney Stone Disease in Autosomal Dominant Polycystic Kidney Disease
You, Zhiying , Brosnahan, Godela , Chapman, Arlene B., Chonchol, Michel , Gitomer, Berenice Y , Wang, Wei , Hopp, Katharina , Nowak, Kristen L. , Perrone, Ronald D. , Torres, Vicente E. , Yu, Alan S.L.

Journal of the American Society of Nephrology | May 17, 2024 | Volume: 33 | Issue: 11S | Pages: 159-159

10.1681/asn.20223311s1159b Get It

Antibiotic Use and Kidney Stone Disease in Patients With Autosomal Dominant Polycystic Kidney Disease
You, Zhiying , Brosnahan, Godela , Jovanovich, Anna, Chapman, Arlene B., Chonchol, Michel , Gitomer, Berenice Y , Wang, Wei , Hopp, Katharina , Nowak, Kristen L. , Jovanovich, Anna J. , Perrone, Ronald D. , Torres, Vicente E. , Yu, Alan S.L.

Journal of the American Society of Nephrology | May 17, 2024 | Volume: 33 | Issue: 11S | Pages: 159-159

10.1681/asn.20223311s1159a Get It

Weight Loss to Slow Cyst Growth in Autosomal Dominant Polycystic Kidney Disease (ADPKD)
Kline, Timothy L. , Wang, Wei , You, Zhiying , Bing, Kristen , Poudyal, Bhavya , Chonchol, Michel , Nowak, Kristen L. , Catenacci, Victoria A. , Steele, Cortney , Gitomer, Berenice Y

Journal of the American Society of Nephrology | May 17, 2024 | Volume: 32 | Issue: 10S | Pages: 404-404

10.1681/asn.20213210s1404a Get It

Overweight and Obesity Are Predictors of Pain in the HALT-PKD Studies
You, Zhiying , Brosnahan, Godela , Miskulin, Dana C. , Steinman, Theodore I., Braun, William E. , Chapman, Arlene B., Chonchol, Michel , Study, HALT-PKD, Wang, Wei Qiang , Gitomer, Berenice Y , Harris, Peter C. , Torres, Vicente E. , Abebe, Kaleab Z , Yu, Alan S.L. , Perrone, Ronald D. , Nowak, Kristen L. , Study, HALT-PKD

Journal of the American Society of Nephrology | May 17, 2024 | Volume: 31 | Issue: 10S | Pages: 500-500

10.1681/asn.20203110s1500a Get It

GG-06 Single cell gene expression studies in lupus patient monocytes reveal novel patterns reflecting disease activity, interferon, and medical treatment
Jin, Zhongbo , Jensen, Mark A, Dorschner, Jessica M., Vsetecka, Danielle, Amin, Shreyasee , Ernste, Floranne C. , Osborn, Thomas G. , Moder, Kevin G., Chowdhary, Vaidehi , Fan, Wei, Jensen, Mark A, Makol, Ashima , Niewold, Timothy B.

Genetics, Genomics and Epigenetics | May 14, 2024 | Volume: No volume available | Issue: No issue available | Pages: A30.1-A30

10.1136/lupus-2016-000179.58 Get It

Single-cell analysis of anti-BCMA CAR T cell therapy in patients with central nervous system autoimmunity
Qin, Chuan , Zhang, Min , Mou, Dapeng , Zhou, Luo‐Qi , Dong, Ming‐Hao , Huang, Liang , Wang, Wen , Cai, Song-Bai , You, Yun‐Fan , Shang, Ke , Xiao, Jun , Wang, Di , Li, Chunrui , Hao, Yi , Wu, Long‐Jun , Bu, Bi-Tao, Wang, Wei , Li, Chun-Rui , Heming, Michael , Wu, Long-Jun , Meyer Zu Hörste, Gerd , Dong, Chen , Bu, Bi-Tao , Tian, Dai-Shi , Wang, Wei , Wang, Wen , Tian, Dai‐Shi

Science Immunology | May 10, 2024 | Volume: 9 | Issue: 95 | Pages: No page available

10.1126/sciimmunol.adj9730 | PMID 38728414 Get It

Chimeric antigen receptor (CAR) T cell immunotherapy for the treatment of neurological autoimmune diseases is promising, but CAR T cell kinetics and immune alterations after treatment are poorly understood. Here, we performed single-cell multi-omics sequencing of paired cerebrospinal fluid (CSF) and blood samples from patients with neuromyelitis optica spectrum disorder (NMOSD) treated with anti–B cell maturation antigen (BCMA) CAR T cells. Proliferating cytotoxic-like CD8 + CAR T cell clones were identified as the main effectors in autoimmunity. Anti-BCMA CAR T cells with enhanced features of chemotaxis efficiently crossed the blood-CSF barrier, eliminated plasmablasts and plasma cells in the CSF, and suppressed neuroinflammation. The CD44-expressing early memory phenotype in infusion products was potentially associated with CAR T cell persistence in autoimmunity. Moreover, CAR T cells from patients with NMOSD displayed distinctive features of suppressed cytotoxicity compared with those from hematological malignancies. Thus, we provide mechanistic insights into CAR T cell function in patients with neurological autoimmune disease.
clinical, laboratory and trichoscopic features of pediatric androgenetic alopecia: a retrospective analysis in 133 patients
Lu, Changpei, Fan, Yige, Du, Yimei , Bi, Lingbo , Wang, Chaofan , Zhao, Min , Ding, yunbu, Wei-xin, FAN, Ding, Yunbu , Wei-xin, FAN

No container title available | May 2, 2024 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.21203/rs.3.rs-4312979/v1 Get It

Abstract This retrospective study from Jiangsu Province Hospital elucidates the prevalence and impact of pediatric androgenetic alopecia (AGA). Over a period of 14 years, 133 patients under the age of 18 were studied, with manifestations appearing as early as 8 years of age. Of note, 39.8% had an overweight/obese and 78.2% reported a family history of AGA. Comorbidities included seborrhoeic dermatitis (51.9%), acne (42.9%) and sleep disorders (28.6%). In addition, 4.5% had polycystic ovarian syndrome. Hormonal imbalances such as low sex hormone-binding globulin (47.1%) and vitamin D deficiency (61%) were common, as was low ferritin (23.6%). Male AGA patterns were characterised by crown thinning and temporal variations, whereas females showed crown thinning with frontal hair retention. Trichoscopic differences were observed between genders and age groups. This study highlights the importance of individualised, stepwise and comprehensive treatment, prioritising hormonal disorders and comorbidities when treating hair loss with topical minoxidil. Encouraging patients to adhere to regular medication and follow-up appointments can lead to favourable outcomes.