BRAF V600E mutations are common in pleomorphic xanthoastrocytoma: diagnostic and therapeutic implications von Dias-Santagata, Dora, Lam, Quynh, Vernovsky, Kathy, Vena, Natalie, Lennerz, Jochen K, Borger, Darrell R, Batchelor, Tracy T, Ligon, Keith L, Iafrate, A John, Ligon, Azra H, Louis, David N, Santagata, Sandro

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Mortality in sickle cell anemia in Africa: a prospective cohort study in Tanzania von Makani, Julie, Cox, Sharon E, Soka, Deogratius, Komba, Albert N, Oruo, Julie, Mwamtemi, Hadija, Magesa, Pius, Rwezaula, Stella, Meda, Elineema, Mgaya, Josephine, Lowe, Brett, Muturi, David, Roberts, David J, Williams, Thomas N, Pallangyo, Kisali, Kitundu, Jesse, Fegan, Gregory, Kirkham, Fenella J, Marsh, Kevin, Newton, Charles R

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College of American Pathologists' laboratory standards for next-generation sequencing clinical tests von Aziz, Nazneen, Zhao, Qin, Bry, Lynn, Driscoll, Denise K, Funke, Birgit, Gibson, Jane S, Grody, Wayne W, Hegde, Madhuri R, Hoeltge, Gerald A, Leonard, Debra G B, Merker, Jason D, Nagarajan, Rakesh, Palicki, Linda A, Robetorye, Ryan S, Schrijver, Iris, Weck, Karen E, Voelkerding, Karl V

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Pathology in the Medical Profession?: Taking the Pulse of Physician Wellness and Burnout von Schrijver, Iris

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Advantages and challenges of online translation teaching and learning during the Covid-19 pandemic: A Mexican case study von Libreros, Cortez, Schrijver, Iris

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Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China von Yuan, Yongyi, Guo, Weiwei, Tang, Jie, Zhang, Guozheng, Wang, Guojian, Han, Mingyu, Zhang, Xun, Yang, Shiming, He, David Z Z, Dai, Pu

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Clinical heterogeneity of duchenne muscular dystrophy (DMD): definition of sub-phenotypes and predictive criteria by long-term follow-up von Desguerre, Isabelle, Christov, Christo, Mayer, Michele, Zeller, Reinhard, Becane, Henri-Marc, Bastuji-Garin, Sylvie, Leturcq, France, Chiron, Catherine, Chelly, Jamel, Gherardi, Romain K

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A two-antibody mismatch repair protein immunohistochemistry screening approach for colorectal carcinomas, skin sebaceous tumors, and gynecologic tract carcinomas von Mojtahed, Amirkaveh, Schrijver, Iris, Ford, James M, Longacre, Teri A, Pai, Reetesh K

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Synergistic post-transcriptional regulation of the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) by miR-101 and miR-494 specific binding von Megiorni, Francesca, Cialfi, Samantha, Dominici, Carlo, Quattrucci, Serena, Pizzuti, Antonio

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Adaptive evolution of Staphylococcus aureus during chronic endobronchial infection of a cystic fibrosis patient von McAdam, Paul R, Holmes, Anne, Templeton, Kate E, Fitzgerald, J Ross

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Prevalence and clinical features of hearing loss patients with CDH23 mutations: a large cohort study von Miyagawa, Maiko, Nishio, Shin-ya, Usami, Shin-ichi

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Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: a prospective population-based cohort study von Su, Yi-Ning, Hung, Chia-Cheng, Lin, Shin-Yu, Chen, Fang-Yi, Chern, Jimmy P S, Tsai, Chris, Chang, Tai-Sheng, Yang, Chih-Chao, Li, Hung, Ho, Hong-Nerng, Lee, Chien-Nan

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Deficiency of FLCN in mouse kidney led to development of polycystic kidneys and renal neoplasia von Chen, Jindong, Futami, Kunihiko, Petillo, David, Peng, Jun, Wang, Pengfei, Knol, Jared, Li, Yan, Khoo, Sok-Kean, Huang, Dan, Qian, Chao-Nan, Zhao, Ping, Dykema, Karl, Dykyma, Karl, Zhang, Racheal, Cao, Brian, Yang, Ximing J, Furge, Kyle, Williams, Bart O, Teh, Bin Tean

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A systematic review of studies measuring and reporting hearing aid usage in older adults since 1999: a descriptive summary of measurement tools von Perez, Elvira, Edmonds, Barrie A

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The role of the cytoskeleton in the formation of gap junctions by Connexin 30 von Qu, Chunyan, Gardner, Phyllis, Schrijver, Iris

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Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach von Waye, John S, Riemer, Cathy, Gallivan, Monica V E, Kollia, Panagoula, Galanello, Renzo, Perseu, Lucia, Anstee, David J, Faustino, Paula, Harteveld, Cornelis L, Hoyer, James D, Peterson, Kenneth R, Giordano, Piero C, Stojiljkovic, Maja, Schrijver, Iris, Thein, Swee Lay, Gibbons, Richard J, Jarvis, Martin, Hardison, Ross C, Maglott, Donna, Francina, Alain, Borg, Joseph, Wada, Takahito, Basak, A Nazli, Giardine, Belinda, Pavlovic, Sonja, Costa, Flavia C, Papadopoulos, Petros, Old, John, Philipsen, Sjaak, Menzel, Stephan, Higgs, Douglas R, Radmilovic, Milena, Wajcman, Henri, Patrinos, George P, Fedosyuk, Halyna, Georgitsi, Marianthi, Traeger-Synodinos, Jan, Papadakis, Manoussos N, Joly, Philippe, Papachatzopoulou, Adamantia, Tully, Ray, Miller, Webb, Zukic, Branka, Felice, Alex E, Kanavakis, Emmanuel, Singleton, Belinda K, Wiemann, Claudia, Moradkhani, Kamran, Satta, Stefania, Clark, Barnaby, Chui, David H K

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The p.V37I exclusive genotype of GJB2: a genetic risk-indicator of postnatal permanent childhood hearing impairment von Li, Lei, Lu, Jingrong, Tao, Zheng, Huang, Qi, Chai, Yongchuan, Li, Xiaohua, Huang, Zhiwu, Li, Yun, Xiang, Mingliang, Yang, Jun, Yao, Guoyin, Wang, Yu, Yang, Tao, Wu, Hao

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Optimal electrical properties of outer hair cells ensure cochlear amplification von Nam, Jong-Hoon, Fettiplace, Robert

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Predisposition for and prevention of subjective tinnitus development von Ahlf, Sönke, Tziridis, Konstantin, Korn, Sabine, Strohmeyer, Ilona, Schulze, Holger

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Mutation detection by real-time PCR: a simple, robust and highly selective method von Morlan, John, Baker, Joffre, Sinicropi, Dominick

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