Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 307 Records) |
Query Trace: VHL[original query] |
---|
Genotype-Phenotype Correlations and Clinical Outcomes in 155 Cases of Pheochromocytoma and Paraganglioma. World journal of surgery 2022 12 47 (3): 690-698. Wang Hogan, Papachristos Alexander J, Gill Anthony J, Clifton-Bligh Roderick, Aniss Ahmad M, Glover Anthony, Sywak Mark, Sidhu Stan |
The germline mutational landscape of genitourinary cancers and its indication for prognosis and risk. BMC urology 2022 11 22 (1): 196. Yang Yong, Zhang Guoying, Hu Chen, Luo Wei, Jiang Haiyang, Liu Shaoyou, Yang Ho |
A Rare Case of Synchronous Fumarate Hydratase-Deficient Renal Cell Carcinoma and Clear Cell Renal Cell Carcinoma With Fumarate Hydratase and von Hippel-Lindau Gene Mutations: A Clinicopathologic and Molecular Study. International journal of surgical pathology 2023 9 10668969231195072. Hui Wen, Linmao Zheng, Mengxin Zhang, Xiuyi Pan, Duohao Wang, Jinyu Qian, Xingming Zhang, Qiao Zhou, Ni Ch |
Hereditary Renal Cell Carcinoma: Is Age an Independent Criterion for Genetic Testing? A Large Cohort from a Latin America Referral Center. Journal of kidney cancer and VHL 2023 8 10 (3): 17-22. Tomás Carminatti, Patricio Aitor García Marchiñena, Ignacio Pablo Tobia González, Valeria de Miguel, Marcelo Martín Serra, Pablo Germán Kalfayan, Alberto Manuel Jura |
Cerebrospinal fluid as a liquid biopsy for molecular characterization of brain metastasis in patients with non-small cell lung cancer. Lung cancer (Amsterdam, Netherlands) 2023 7 182 107292. Georgios Tsakonas, Vasisht Tadigotla, Sudipto K Chakrabortty, Giuseppe Stragliotto, Dalin Chan, Rolf Lewensohn, Wei Yu, Johan K Skog, Per Hydbring, Simon Ekm |
Gene mutation profiling and clinical significances in patients with renal cell carcinoma. Clinics (Sao Paulo, Brazil) 2023 7 78 100259. Yongquan Wang, Peng He, Xiaozhou Zhou, Cong Wang, Jian Fu, Dawei Zhang, Deyang Liao, Zhansong Zhou, Chunman Wu, Wei Go |
Potential Role of VHL, PTEN, and BAP1 Mutations in Renal Tumors. Journal of clinical medicine 2023 7 12 (13): . Krisztián Szegedi, Zsuzsanna Szabó, Judit Kállai, József Király, Erzsébet Szabó, Zsuzsanna Bereczky, Éva Juhász, Balázs Dezs?, Csaba Szász, Barbara Zsebik, Tibor Flaskó, Gábor Halm |
Increased transferrin protects from thrombosis in Chuvash erythrocytosis. American journal of hematology 2023 7 . Binal N Shah, Xu Zhang, Adelina I Sergueeva, Galina Y Miasnikova, Tomas Ganz, Josef T Prchal, Victor R Gorde |
Whole Exome Sequencing Reveals Novel Variants in Unexplained Erythrocytosis. Omics : a journal of integrative biology 2023 7 . Harshit Khurana, Babylakshmi Muthusamy, Uday Yanamandra, Kishore Garapati, Harikrishnan Premdeep, Shankar Subramanian, Akhilesh Pand |
Genomic profiles of renal cell carcinoma in a small Chinese cohort. Frontiers in oncology 2023 7 13 1095775. Sheng Tai, Dan-Dan Xu, Zhixian Yu, Yu Guan, Shuiping Yin, Jun Xiao, Song Xue, Chaozhao Lia |
A Screening Approach for Inherited Erythrocytosis due to the VHL:c.598C?>?T Mutation (Chuvash Polycythemia). Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2023 6 1-5. Nisha Duggal, Namrata Singh, Suchet Sachdev, Avinash Kumar Singh, Jasbir Kaur Hira, Sanjeev Chhabra, Deepak Bansal, Pankaj Malhotra, Neelam Varma, Reena Das, Prashant Shar |
Genotype-phenotype associations in paragangliomas of the temporal bone in a multi-ethnic cohort. Acta oto-laryngologica 2023 6 1-7. Simon I Angeli, Juan A Chiossone K, Stefania Goncalves, Fred F Telisc |
The value of molecular testing in the evaluation and management of patients with pancreatic cysts. Diagnostic cytopathology 2023 6 . Suzanne M Selvag |
Genomic analysis of plasma circulating tumor DNA in patients with heavily pretreated HER2?+?metastatic breast cancer. Scientific reports 2023 6 13 (1): 9928. Kyoungmin Lee, Jongwon Lee, Jungmin Choi, Sung Hoon Sim, Jeong Eun Kim, Min Hwan Kim, Yeon Hee Park, Jee Hyun Kim, Su-Jin Koh, Kyong Hwa Park, Myoung Joo Kang, Mi Sun Ahn, Kyoung Eun Lee, Hee-Jun Kim, Hee Kyung Ahn, Han Jo Kim, Keon Uk Park, In Hae Pa |
Genetic mutations in HER2-positive breast cancer: possible association with response to trastuzumab therapy. Human genomics 2023 5 17 (1): 43. Nermine H Zakaria, Doaa Hashad, Marwa H Saied, Neamat Hegazy, Alyaa Elkayal, Eman Tay |
Clear cell renal cell carcinoma molecular variations in non-Hispanic White and Hispanic patients. Cancer medicine 2023 4 . Ken Batai, Yuliang Chen, Brenna A Rheinheimer, Amit Arora, Ritu Pandey, Ronald L Heimark, Erika R Bracamonte, Nathan A Ellis, Benjamin R L |
Genotype-phenotype correlations and clinical outcomes of patients with von Hippel-Lindau disease with large deletions. Journal of medical genetics 2023 4 60 (5): 477-483. Kenan Zhang, Wuping Yang, Kaifang Ma, Jianhui Qiu, Lei Li, Yawei Xu, Zedan Zhang, Chaojian Yu, Jingcheng Zhou, Yanqing Gong, Lin Cai, Kan Go |
Domain landscapes of somatic NF1 mutations in pheochromocytoma and paraganglioma. Gene 2023 4 147432. Tabebi Mouna, Frikha Fakher, Volpe Massimiliano, Gimm Oliver, Söderkvist Pet |
Prevalence of germline mutations in cancer susceptibility genes in Chinese patients with renal cell carcinoma. Translational andrology and urology 2023 3 12 (2): 308-319. Feng Huayi, Cao Shouqing, Ouyang Qing, Li Huaikang, Li Xiubin, Chen Ke, Zhang Xiangyi, Huang Yan, Zhang Xu, Ma X |
Two Single Nucleotide Polymorphisms in the Von Hippel-Lindau Tumor Suppressor Gene in Patients with Clear Cell Renal Cell Carcinoma. International journal of molecular sciences 2023 2 24 (4): . Chraba?ska Magdalena, Szweda-Gandor Nikola, Drozdzowska Bog |
Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma. Clinical cancer research : an official journal of the American Association for Cancer Research 2023 2 OF1-OF12. Vasudev Naveen S, Scelo Ghislaine, Glennon Kate I, Wilson Michelle, Letourneau Louis, Eveleigh Robert, Nourbehesht Nazanin, Arseneault Madeleine, Paccard Antoine, Egevad Lars, Viksna Juris, Celms Edgars, Jackson Sharon M, Abedi-Ardekani Behnoush, Warren Anne Y, Selby Peter J, Trainor Sebastian, Kimuli Michael, Cartledge Jon, Soomro Naeem, Adeyoju Adebanji, Patel Poulam M, Wozniak Magdalena B, Holcatova Ivana, Brisuda Antonin, Janout Vladimir, Chanudet Estelle, Zaridze David, Moukeria Anush, Shangina Oxana, Foretova Lenka, Navratilova Marie, Mates Dana, Jinga Viorel, Bogdanovic Ljiljana, Kovacevic Bozidar, Cambon-Thomsen Anne, Bourque Guillaume, Brazma Alvis, Tost Jörg, Brennan Paul, Lathrop Mark, Riazalhosseini Yasser, Banks Rosamonde |
Prostate Cancer Patient Stratification by Molecular Signatures in the Veterans Precision Oncology Data Commons. Cold Spring Harbor molecular case studies 2023 12 . Kyle M Hernandez, Aarti Venkat, Danne C Elbers, John R Bihn, Mary T Brophy, Nhan V Do, Jennifer La, Qiong Liu, Andrew Prokhorenkov, Noah Metoki-Shlubsky, Feng-Chi Sung, Channing J Paller, Nathanael R Fillmore, Robert L Grossm |
Pathogenic Germline Mutational Landscape in Patients With Renal Cell Carcinoma and Associated Clinicopathologic Features. JCO precision oncology 2023 12 7 e2300168. Charles B Nguyen, Claire Knaus, Jinju Li, Marie-Louise Accardo, Erika Koeppe, Ulka N Vaishampayan, Ajjai S Alva, Tobias El |
Does the VHL polymorphisms rs779805 and rs1642742 affect renal cell carcinoma susceptibility, prognosis and survival in Central European population? Medicine 2023 12 102 (50): e36540. Magdalena Chraba?ska, Nikola Szweda-Gandor, Bogna Drozdzows |
Integrative Analysis of Germline Rare Variants in Clear and Non-Clear Cell Renal Cell Carcinoma. medRxiv : the preprint server for health sciences 2023 1 . Han Seunghun, Camp Sabrina Y, Chu Hoyin, Collins Ryan, Gillani Riaz, Park Jihye, Bakouny Ziad, Ricker Cora A, Reardon Brendan, Moore Nicholas, Kofman Eric, Labaki Chris, Braun David, Choueiri Toni K, AlDubayan Saud H, Van Allen Eliezer |
SDHB exon 1 deletion: A recurrent germline mutation in Colombian patients with pheochromocytomas and paragangliomas. Frontiers in genetics 2023 1 13 999329. Manotas María Carolina, Rivera Ana Lucía, Gómez Ana Milena, Abisambra Patricia, Guevara Gonzalo, Medina Vilma, Tapiero Sandra, Huertas Antonio, Riaño-Moreno Julián, Mejía Juan Carlos, Gonzalez-Clavijo Angélica María, Tapiero-García Mireya, Cuéllar-Cuéllar Andrés Arturo, Fierro-Maya Luis Felipe, Sanabria-Salas María Caroli |
Frequency of Pathogenic Germline Mutations in Early and Late Onset Familial Breast Cancer Patients Using Multi-Gene Panel Sequencing: An Egyptian Study. Genes 2023 1 14 (1): . Nassar Auhood, Zekri Abdel-Rahman N, Kamel Mahmoud M, Elberry Mostafa H, Lotfy Mai M, Seadawy Mohamed G, Hassan Zeinab K, Soliman Hany K, Lymona Ahmed M, Youssef Amira Salah El-D |
Diagnostic Approaches to Investigate JAK2-Unmutated Erythrocytosis Based on a Single Tertiary Center Experience. Molecular diagnosis & therapy 2024 4 . Youngeun Lee, Soo Hyun Seo, Jinho Kim, Sang-A Kim, Ji Yun Lee, Jeong-Ok Lee, Soo-Mee Bang, Kyoung Un Park, Sang Mee Hwa |
Chromosome 3p gene alterations as biomarkers for immunocombinations in metastatic renal cell carcinoma: A hypothesis-generating analysis. Pathology, research and practice 2024 1 254 155142. Matteo Rosellini, Veronica Mollica, Andrea Marchetti, Sara Coluccelli, Francesca Giunchi, Elisa Tassinari, Costantino Ricci, Michelangelo Fiorentino, Giovanni Tallini, Dario De Biase, Francesco Massa |
Analysis of HIF-1? expression and genetic polymorphisms in human clear cell renal cell carcinoma. Pathology oncology research : POR 2024 1 29 1611444. Daniela Vargova, Zuzana Kolková, Jan Dargaj, Lukas Bris, Jan Luptak, Zuzana Dankova, Sona Franova, Jan Svihra, Pavol Slávik, Martina Sutovs |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
- Content source: