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Frank Mentch

children's hospital of philadelphia

44H指数
201论文数
1.2W被引数
收录论文 93
发表时间
Unsupervised Deep Representation Learning and Probabilistic Clustering for the Systems-Level Discovery of Germline Mutation Signatures in Pediatric Cancers基于无监督深度表示学习和概率聚类的儿童癌症体细胞突变签名系统级发现
err2026-06-25
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errOAAI
errFahimeh Palizban; Michael E. March; Xiang Wang; James Snyder; Fengxiang Wang; Frank Mentch; Yeshwanth Mahesh; Alexandria Thomas; Deborah J. Watson; Huiqi Qu; John Connolly; Amir Hossein Saeidian; Hassan Vahidnezhad; Joseph Glessner; Hakon Hakonarson
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Multitrait GWAS and functional validation reveal genetic loci for gastric cancer多性状全基因组关联研究及功能验证揭示了胃癌的遗传位点
err2026-03-15
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errHuanxin Ding; Chuxuan Liu; Qing Sun; Yue Jiang; Qian Xu; Zhenguo Zhu; Xin Jin; Qibo Huang; Yue Li; Yingchao Song; Zenglin Liu; Tianming Yu; Bowen Shi; Delin Tan; Linzehao Li; Frank Mentch; Joseph Glessner; Xiao Chang; Hakon Hakonarson; Guangyong Zhang
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APOL1 kidney risk variants and outcomes in children with congenital anomalies of the kidney and urinary tract先天性肾脏和尿路异常儿童的APOL1肾脏风险变异和结局
err2026-01-14
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PREAI
errLisanne M. Vendrig; Juntao Ke; Michael W. T. Tanck; Tze Y. Lim; Elena Martinelli; Monica Bodria; Valentina Capone; Claudia Izzi; Claudio La Scola; Umberto Maggiore; Pierluigi Marzuillo; Giuseppe Masnata; Frank D. Mentch; Giovanni Montini; Isabella Pisani; Huiqi Qu; Matthew G. Sampson; Ana Cristina Simões-e-Silva; Alexandria Thomas; Jaap W. Groothoff; Hakon Hakonarson; Gian Marco Ghiggeri; Miguel Verbitsky; Elena N. Levtchenko; Simone Sanna-Cherchi; Rik Westland
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Genetic analysis of two bladder exstrophy populations of South Asian and North American origin南亚和北美来源的两个膀胱外翻人群的遗传分析
err2025-12-01
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errWeaver, John K.; Weiss, Dana A.; Thompson, Austin; Joshi, Rakesh; Ramji, Jaishri; Shukla, Aseem R.; D'Souza, Neeta; Kim, Erin; Lee, Joonsue; Wu, Chen-Han Wilfred; Broms, Reiley; Glessner, Joseph; Mentch, Frank; Hakonarson, Hakon; Pyle, Louise C.
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Sex-specific spirometry effects of adult COPD polygenic score in children with asthma成人COPD多基因评分对哮喘儿童的性别特异性肺功能影响
err2025-04-02
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errKelchtermans, Jelte; Collaco, Joseph M.; Qu, Huiqi; Mentch, Frank; McGrath-Morrow, Sharon A.; Hakonarson, Hakon
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Integration of GWAS, QTLs and keratinocyte functional assays reveals molecular mechanisms of atopic dermatitis整合全基因组关联研究、数量性状基因座和角质形成细胞功能实验揭示了特应性皮炎的分子机制
err2025-04-01
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errOliva, Meritxell; Sarkar, Mrinal K.; March, Michael E.; Saeidian, Amir Hossein; Mentch, Frank D.; Hsieh, Chen-Lin; Tang, Fanying; Uppala, Ranjitha; Patrick, Matthew T.; Li, Qinmengge; Bogle, Rachael; Kahlenberg, J. Michelle; Watson, Deborah; Glessner, Joseph T.; Youssefian, Leila; Vahidnezhad, Hassan; Tsoi, Lam C.; Gudjonsson, Johann E.; Smith, Kathleen M.; Riley-Gillis, Bridget
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Insights from the largest diverse ancestry sex-specific disease map for genetically predicted height基于遗传预测身高所得的最大异质性祖先别特异性疾病图谱的见解
err2025-02-27
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errPapadopoulou, A.; Litkowski, E. M.; Graff, M.; Wang, Z.; Smit, R. A. J.; Chittoor, G.; Dinsmore, I.; Josyula, N. S.; Lin, M.; Shortt, J.; Zhu, W.; Vedantam, S. L.; Yengo, L.; Wood, A. R.; Berndt, S. I.; Holm, I. A.; Mentch, F. D.; Hakonarson, H.; Kiryluk, K.; Weng, C.; Jarvik, G. P.; Crosslin, D.; Carrell, D.; Kullo, I. J.; Dikilitas, O.; Hayes, M. G.; Wei, W. Q.; Edwards, D. R. V.; Assimes, T. L.; Hirschhorn, J. N.; Below, J. E.; Gignoux, C. R.; Justice, A. E.; Loos, R. J. F.; Sun, Y. V.; Raghavan, S.; Deloukas, P.; North, K. E.; Marouli, E.
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The genetic landscape of pediatric postural orthostatic tachycardia syndrome
err2025-02-18
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errQu, Huiqi; Qu, Jingchun; Chang, Xiao; Williams, Nolan; Mentch, Frank; Snyder, James; Lemma, Maria; Nguyen, Kenny; Behr, Meckenzie; March, Michael; Connolly, John; Glessner, Joseph; Boris, Jeffrey R.; Hakonarson, Hakon
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Correspondence on Weighty matters: Considering the ethics of genetic risk scores for obesity by C. Houtz重要事项往来函:C. Houtz撰写的《关于肥胖遗传风险评分的伦理考量》
err2024-11-01
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PREAI
errConnolly, John J.; Hess, Molly; Maripuri, Priyanka; Terek, Shannon; Purcell, Jasmine; Harr, Margaret H.; Mentch, Frank D.; Glessner, Joseph T.; Shah, Rachana; Prows, Cindy A.; Karavite, Dean J.; Thayer, Jeritt G.; Grundmeier, Robert W.
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Identification of genetic variants associated with clinical features of sickle cell disease鉴定与镰状细胞病临床特征相关的遗传变异
err2024-08-29
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errTsukahara, Katharine; Chang, Xiao; Mentch, Frank; Smith-Whitley, Kim; Bhandari, Anita; Norris, Cindy; Glessner, Joseph T.; Hakonarson, Hakon
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Copy number variations contribute to malignant tumor development in children with serious birth defects严重出生缺陷儿童的拷贝数变异有助于恶性肿瘤的发展
err2024-08-14
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errLiu, Yichuan; Glessner, Joseph; Qu, Hui-Qi; Chang, Xiao; Qiu, Haijun; Wang, Tiancheng; Mentch, Frank D.; Hakonarson, Hakon
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Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes (vol 25, 22, 2024)纵向青春期身高增长和共享遗传力与成人健康结果的跨祖先全基因组关联研究 (第25、22、2024卷)
err2024-05-21
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errBradfeld, Jonathan P.; Kember, Rachel L.; Ulrich, Anna; Balkhiyarova, Zhanna; Alyass, Akram; Aris, Izzuddin M.; Bell, Joshua A.; Broadaway, Alaine; Chen, Zhanghua; Chai, Jin-Fang; Davies, Neil M.; Fernandez-Orth, Dietmar; Bustamante, Mariona; Fore, Ruby; Ganguli, Amitavo; Heiskala, Anni; Hottenga, Jouke-Jan; Iniguez, Carmen; Kobes, Sayuko; Leinonen, Jaakko; Lowry, Estelle; Lyytikainen, Leo-Pekka; Mahajan, Anubha; Pitkanen, Niina; Schnurr, Theresia M.; Have, Christian Theil; Strachan, David P.; Thiering, Elisabeth; Vogelezang, Suzanne; Wade, Kaitlin H.; Wang, Carol A.; Wong, Andrew; Holm, Louise Aas; Chesi, Alessandra; Choong, Catherine; Cruz, Miguel; Elliott, Paul; Franks, Steve; Frithiof-Bojsoe, Christine; Gauderman, W. James; Glessner, Joseph T.; Gilsanz, Vicente; Griesman, Kendra; Hanson, Robert L.; Kaakinen, Marika; Kalkwarf, Heidi; Kelly, Andrea; Kindler, Joseph; Kahonen, Mika; Lanca, Carla; Lappe, Joan; Lee, Nanette R.; McCormack, Shana; Mentch, Frank D.; Mitchell, Jonathan A.; Mononen, Nina; Niinikoski, Harri; Oken, Emily; Pahkala, Katja; Sim, Xueling; Teo, Yik-Ying; Baier, Leslie J.; Van Beijsterveldt, Toos; Adair, Linda S.; Boomsma, Dorret I.; De Geus, Eco; Guxens, Monica; Eriksson, Johan G.; Felix, Janine F.; Gilliland, Frank D.; Hansen, Torben; Hardy, Rebecca; Hivert, Marie-France; Holm, Jens-Christian; Jaddoe, Vincent W. V.; Jarvelin, Marjo-Riitta; Lehtimaki, Terho; Mackey, David A.; Meyre, David; Mohlke, Karen L.; Mykkanen, Juha; Oberfeld, Sharon; Pennell, Craig E.; Perry, John R. B.; Raitakari, Olli; Rivadeneira, Fernando; Saw, Seang-Mei; Sebert, Sylvain; Shepherd, John A.; Standl, Marie; Sorensen, Thorkild I. A.; Timpson, Nicholas J.; Torrent, Maties; Willemsen, Gonneke; Hypponen, Elina; Power, Chris; McCarthy, Mark I.; Freathy, Rachel M.; Widen, Elisabeth; Hakonarson, Hakon; Prokopenko, Inga; Voight, Benjamin F.; Zemel, Babette S.; Grant, Struan F. A.; Cousminer, Diana L.
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High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number Variations出生缺陷患者中儿童癌症的高合并症: 来自拷贝数变异的全基因组测序分析的见解
err2024-04-01
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PREAI
errQu, Hui-Qi; Glessner, Joseph T.; Qu, Jingchun; Liu, Yichuan; Watson, Deborah; Chang, Xiao; Saeidian, Amir Hossein; Qiu, Haijun; Mentch, Frank; Connolly, John J.; Kakoharson, Hakon
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Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes纵向青春期身高增长和共享遗传力与成人健康结果的跨祖先全基因组关联研究
err2024-01-16
err4
errOAAI
errBradfield, Jonathan P.; Kember, Rachel L.; Ulrich, Anna; Balkiyarova, Zhanna; Alyass, Akram; Aris, Izzuddin M.; Bell, Joshua A.; Broadaway, K. Alaine; Chen, Zhanghua; Chai, Jin-Fang; Davies, Neil M.; Fernandez-Orth, Dietmar; Bustamante, Mariona; Fore, Ruby; Ganguli, Amitavo; Heiskala, Anni; Hottenga, Jouke-Jan; Iniguez, Carmen; Kobes, Sayuko; Leinonen, Jaakko; Lowry, Estelle; Lyytikainen, Leo-Pekka; Mahajan, Anubha; Pitkanen, Niina; Schnurr, Theresia M.; Have, Christian Theil; Strachan, David P.; Thiering, Elisabeth; Vogelezang, Suzanne; Wade, Kaitlin H.; Wang, Carol A.; Wong, Andrew; Holm, Louise Aas; Chesi, Alessandra; Choong, Catherine; Cruz, Miguel; Elliott, Paul; Franks, Steve; Frithioff-Bojsoe, Christine; Gauderman, W. James; Glessner, Joseph T.; Gilsanz, Vicente; Griesman, Kendra; Hanson, Robert L.; Kaakinen, Marika; Kalkwarf, Heidi; Kelly, Andrea; Kindler, Joseph; Kahonen, Mika; Lanca, Carla; Lappe, Joan; Lee, Nanette R.; McCormack, Shana; Mentch, Frank D.; Mitchell, Jonathan A.; Mononen, Nina; Niinikoski, Harri; Oken, Emily; Pahkala, Katja; Sim, Xueling; Teo, Yik-Ying; Baier, Leslie J.; van Beijsterveldt, Toos; Adair, Linda S.; Boomsma, Dorret, I; de Geus, Eco; Guxens, Monica; Eriksson, Johan G.; Felix, Janine F.; Gilliland, Frank D.; Biobank, Penn Medicine; Hansen, Torben; Hardy, Rebecca; Hivert, Marie-France; Holm, Jens-Christian; Jaddoe, Vincent W. V.; Jarvelin, Marjo-Riitta; Lehtimaki, Terho; Mackey, David A.; Meyre, David; Mohlke, Karen L.; Mykkanen, Juha; Oberfield, Sharon; Pennell, Craig E.; Perry, John R. B.; Raitakari, Olli; Rivadeneira, Fernando; Saw, Seang-Mei; Sebert, Sylvain; Shepherd, John A.; Standl, Marie; Sorensen, Thorkild I. A.; Timpson, Nicholas J.; Torrent, Maties; Willemsen, Gonneke; Hypponen, Elina; Power, Chris; McCarthy, Mark, I; Freathy, Rachel M.; Widen, Elisabeth; Hakonarson, Hakon; Prokopenko, Inga; Voight, Benjamin F.; Zemel, Babette S.; Grant, Struan F. A.; Cousminer, Diana L.
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