Citations

Citations to this article as recorded by  

• EBUS-TBNA pleural biopsy reveals prostate cancer metastasis: A rare case report and review of the literature
  Fotios Sampsonas, Dimitrios Komninos, Vasilina Sotiropoulou, Matthaios Katsaras, Dimitra Gkanetsou, Ourania Papaioannou, Panagiota Tsiri, Vasiliki Tzelepi, Argyrios Tzouvelekis
  Pneumon.2024; 37(2): 1.     CrossRef
• Cytopathological Features of Extensive Bilateral Pleural Effusions in Metastatic Prostate Cancer: Report of a Rare Case
  Hehua Huang, Caroline Yap
  Cureus.2024;[Epub]     CrossRef
• Bilateral pleural effusion: etiology, diagnostics
  N. A. Stogova
  PULMONOLOGIYA.2022; 32(6): 885.     CrossRef
• Rare Metastatic Prostate Cancer Mimicking Lymphoma with Malignant Pleural Effusion
  Tung Liu, En Meng, Yu-Chun Lin, Tai-Kuang Chao, Yi-Ming Chang
  Journal of Medical Sciences.2021; 42(1): 46.     CrossRef

Citations

Citations to this article as recorded by  

• Enhancing Lung Cancer Care in Portugal: Bridging Gaps for Improved Patient Outcomes
  Raquel Ramos, Conceição Souto Moura, Mariana Costa, Nuno Jorge Lamas, Renato Correia, Diogo Garcez, José Miguel Pereira, Carlos Sousa, Nuno Vale
  Journal of Personalized Medicine.2024; 14(5): 446.     CrossRef
• Evolution of therapy for ALK-positive lung carcinomas: Application of third-generation ALK inhibitors in real clinical practice
  A. F. Nasretdinov, A. V. Sultanbaev, Sh. I. Musin, K. V. Menshikov, R. T. Ayupov, A. A. Izmailov, G. A. Serebrennikov, V. E. Askarov, D. V. Feoktistov
  Meditsinskiy sovet = Medical Council.2024; (10): 74.     CrossRef
• Cost-effectiveness of next-generation sequencing for advanced EGFR/ALK-negative non-small cell lung cancer
  Dong-Won Kang, Sun-Kyeong Park, Sokbom Kang, Eui-Kyung Lee
  Lung Cancer.2024; 197: 107970.     CrossRef
• miR-92a-3p regulates cisplatin-induced cancer cell death
  Romain Larrue, Sandy Fellah, Nihad Boukrout, Corentin De Sousa, Julie Lemaire, Carolane Leboeuf, Marine Goujon, Michael Perrais, Bernard Mari, Christelle Cauffiez, Nicolas Pottier, Cynthia Van der Hauwaert
  Cell Death & Disease.2023;[Epub]     CrossRef
• Diagnostic Approach of Lung Cancer: A Literature Review
  Jesi Hana, Novia Nurul Faizah
  Jurnal Respirasi.2023; 9(2): 141.     CrossRef
• Molecular Pathology of Lung Cancer
  James J. Saller, Theresa A. Boyle
  Cold Spring Harbor Perspectives in Medicine.2022; 12(3): a037812.     CrossRef
• Landscape of EGFR mutations in lung adenocarcinoma: a single institute experience with comparison of PANAMutyper testing and targeted next-generation sequencing
  Jeonghyo Lee, Yeon Bi Han, Hyun Jung Kwon, Song Kook Lee, Hyojin Kim, Jin-Haeng Chung
  Journal of Pathology and Translational Medicine.2022; 56(5): 249.     CrossRef
• Molecular biomarker testing for non–small cell lung cancer: consensus statement of the Korean Cardiopulmonary Pathology Study Group
  Sunhee Chang, Hyo Sup Shim, Tae Jung Kim, Yoon-La Choi, Wan Seop Kim, Dong Hoon Shin, Lucia Kim, Heae Surng Park, Geon Kook Lee, Chang Hun Lee
  Journal of Pathology and Translational Medicine.2021; 55(3): 181.     CrossRef
• TM4SF4 and LRRK2 Are Potential Therapeutic Targets in Lung and Breast Cancers through Outlier Analysis
  Kyungsoo Jung, Joon-Seok Choi, Beom-Mo Koo, Yu Jin Kim, Ji-Young Song, Minjung Sung, Eun Sol Chang, Ka-Won Noh, Sungbin An, Mi-Sook Lee, Kyoung Song, Hannah Lee, Ryong Nam Kim, Young Kee Shin, Doo-Yi Oh, Yoon-La Choi
  Cancer Research and Treatment.2021; 53(1): 9.     CrossRef
• The promises and challenges of early non‐small cell lung cancer detection: patient perceptions, low‐dose CT screening, bronchoscopy and biomarkers
  Lukas Kalinke, Ricky Thakrar, Sam M. Janes
  Molecular Oncology.2021; 15(10): 2544.     CrossRef
• Cost-effectiveness analyses of targeted therapy and immunotherapy for advanced non-small cell lung cancer in the United States: a systematic review
  Anthony Yu, Eva Huang, Momoka Abe, Kang An, Sun-Kyeong Park, Chanhyun Park
  Expert Review of Pharmacoeconomics & Outcomes Research.2021; 21(3): 381.     CrossRef
• The expanding capability and clinical relevance of molecular diagnostic technology to identify and evaluate EGFR mutations in advanced/metastatic NSCLC
  Parth Shah, Jacob Sands, Nicola Normanno
  Lung Cancer.2021; 160: 118.     CrossRef
• Testing for EGFR Mutations and ALK Rearrangements in Advanced Non-Small-Cell Lung Cancer: Considerations for Countries in Emerging Markets
  Mercedes L Dalurzo, Alejandro Avilés-Salas, Fernando Augusto Soares, Yingyong Hou, Yuan Li, Anna Stroganova, Büge Öz, Arif Abdillah, Hui Wan, Yoon-La Choi
  OncoTargets and Therapy.2021; Volume 14: 4671.     CrossRef
• Treatment of Patients With Non–Small-Cell Lung Cancer Harboring Rare Oncogenic Mutations
  Melina E. Marmarelis, Corey J. Langer
  Clinical Lung Cancer.2020; 21(5): 395.     CrossRef
• Detection of Targetable Genetic Alterations in Korean Lung Cancer Patients: A Comparison Study of Single-Gene Assays and Targeted Next-Generation Sequencing
  Eunhyang Park, Hyo Sup Shim
  Cancer Research and Treatment.2020; 52(2): 543.     CrossRef
• High prevalence of ROS1 gene rearrangement detected by FISH in EGFR and ALK negative lung adenocarcinoma
  Yuyin Xu, Heng Chang, Lijing Wu, Xin Zhang, Ling Zhang, Jing Zhang, Yuan Li, Lei Shen, Xiaoli Zhu, Xiaoyan Zhou, Qianming Bai
  Experimental and Molecular Pathology.2020; 117: 104548.     CrossRef
• An All-In-One Transcriptome-Based Assay to Identify Therapy-Guiding Genomic Aberrations in Nonsmall Cell Lung Cancer Patients
  Jiacong Wei, Anna A. Rybczynska, Pei Meng, Martijn Terpstra, Ali Saber, Jantine Sietzema, Wim Timens, Ed Schuuring, T. Jeroen N. Hiltermann, Harry. J.M. Groen, Anthonie van der Wekken, Anke van den Berg, Klaas Kok
  Cancers.2020; 12(10): 2843.     CrossRef
• Immunotherapy in EGFR-Mutant and ALK-Positive Lung Cancer
  Alexander Gavralidis, Justin F. Gainor
  The Cancer Journal.2020; 26(6): 517.     CrossRef
• Role of Immunocytochemistry in the Cytological Diagnosis of Pulmonary Tumors
  Jasna Metovic, Luisella Righi, Luisa Delsedime, Marco Volante, Mauro Papotti
  Acta Cytologica.2020; 64(1-2): 16.     CrossRef
• Molecular Diagnostic Assays and Clinicopathologic Implications of MET Exon 14 Skipping Mutation in Non–small-cell Lung Cancer
  Eun Kyung Kim, Kyung A. Kim, Chang Young Lee, Sangwoo Kim, Sunhee Chang, Byoung Chul Cho, Hyo Sup Shim
  Clinical Lung Cancer.2019; 20(1): e123.     CrossRef
• PD‐L1 expression in ROS1‐rearranged non‐small cell lung cancer: A study using simultaneous genotypic screening of EGFR, ALK, and ROS1
  Jongmin Lee, Chan Kwon Park, Hyoung‐Kyu Yoon, Young Jo Sa, In Sook Woo, Hyo Rim Kim, Sue Youn Kim, Tae‐Jung Kim
  Thoracic Cancer.2019; 10(1): 103.     CrossRef
• Human Leukocyte Antigen Class I and Programmed Death-Ligand 1 Coexpression Is an Independent Poor Prognostic Factor in Adenocarcinoma of the Lung
  Yeon Bi Han, Hyun Jung Kwon, Soo Young Park, Eun-Sun Kim, Hyojin Kim, Jin-Haeng Chung
  Journal of Pathology and Translational Medicine.2019; 53(2): 86.     CrossRef
• Molecular testing for advanced non-small cell lung cancer in Malaysia: Consensus statement from the College of Pathologists, Academy of Medicine Malaysia, the Malaysian Thoracic Society, and the Malaysian Oncological Society
  Pathmanathan Rajadurai, Phaik Leng Cheah, Soon Hin How, Chong Kin Liam, Muhammad Azrif Ahmad Annuar, Norhayati Omar, Noriah Othman, Nurhayati Mohd Marzuki, Yong Kek Pang, Ros Suzanna Ahmad Bustamam, Lye Mun Tho
  Lung Cancer.2019; 136: 65.     CrossRef
• Somatic mutations and immune checkpoint biomarkers
  Brielle A. Parris, Eloise Shaw, Brendan Pang, Richie Soong, Kwun Fong, Ross A. Soo
  Respirology.2019; 24(3): 215.     CrossRef
• Adverse Event Management in Patients with BRAF V600E-Mutant Non-Small Cell Lung Cancer Treated with Dabrafenib plus Trametinib
  Anna Chalmers, Laura Cannon, Wallace Akerley
  The Oncologist.2019; 24(7): 963.     CrossRef
• Genetic and clinicopathologic characteristics of lung adenocarcinoma with tumor spread through air spaces
  Jae Seok Lee, Eun Kyung Kim, Moonsik Kim, Hyo Sup Shim
  Lung Cancer.2018; 123: 121.     CrossRef

Citations

Citations to this article as recorded by  

• Schwann Cell Hamartoma Presenting as a Colonic Polyp: A Rare Case Report With a Literature Review
  Faryal Altaf, Nismat Javed, Haider Ghazanfar, Anil Dev
  Cureus.2024;[Epub]     CrossRef
• Mucosal Schwann Cell Hamartoma Mimicking a Colon Polyp: Pathologic Insights
  Marissa Krizelda Santos, Kathleen Adryon Tan
  PJP.2024;[Epub]     CrossRef
• Multiple non-polypoid mucosal Schwann cell hamartomas presenting as edematous and submucosal tumor-like lesions: a case report
  Takeshi Okamoto, Takaaki Yoshimoto, Katsuyuki Fukuda
  BMC Gastroenterology.2021;[Epub]     CrossRef
• Mucosal Schwann Cell Hamartoma of the Gall Bladder
  Kanika Sharma, Anjan Kumar Dhua, Prabudh Goel, Vishesh Jain, Devendra Kumar Yadav, Prashant Ramteke
  Journal of Indian Association of Pediatric Surgeons.2021; 26(3): 182.     CrossRef
• Mucosal Schwann Cell Hamartoma in sigmoid colon – A rare case report and review of literature
  Xiuyan Feng, Hongzhi Xu, Nestor Dela Cruz
  Human Pathology: Case Reports.2020; 19: 200337.     CrossRef
• Spindle cell proliferations of the sigmoid colon, rectum and anus: a review with emphasis on perineurioma
  Patrice Grech, John B Schofield
  Histopathology.2020; 76(3): 342.     CrossRef
• Mucosal Schwann cell hamartoma of the gastroesophageal junction: A series of 6 cases and comparison with colorectal counterpart
  Yuan Li, Pouneh Beizai, John W. Russell, Lindsey Westbrook, Arash Nowain, Hanlin L. Wang
  Annals of Diagnostic Pathology.2020; 47: 151531.     CrossRef
• Mucosal Schwann Cell Hamartoma Presenting as Diffuse Fine Nodularities
  Han Beol Jang, Jong Ok Kim, Sang-Bum Kang
  The Korean Journal of Gastroenterology.2020; 76(3): 171.     CrossRef
• A case of Schwann cell hamartoma of the tongue
  Saya TAKIKAWA, Shigeo TANAKA, Masamichi KOMIYA, Masaaki SUEMITSU, Tadahiko UTSUNOMIYA, Kayo KUYAMA
  Japanese Journal of Oral and Maxillofacial Surgery.2020; 66(12): 601.     CrossRef
• Hamartoma de células de Schwann mucoso: revisión de una entidad descrita recientemente
  Francisco García-Molina, José Antonio Ruíz-Macia, Joaquin Sola
  Revista Española de Patología.2018; 51(1): 49.     CrossRef
• Neural and neurogenic tumours of the gastroenteropancreaticobiliary tract
  Aoife J McCarthy, Dipti M Karamchandani, Runjan Chetty
  Journal of Clinical Pathology.2018; 71(7): 565.     CrossRef
• Case of colonic mucosal Schwann cell hamartoma and review of literature on unusual colonic polyps
  JayaKrishna Chintanaboina, Kofi Clarke
  BMJ Case Reports.2018; : bcr-2018-224931.     CrossRef

Citations

Citations to this article as recorded by  

• Primary schwannoma of the thyroid gland: analysis of case characteristics and review of the literature
  Hangjun Ren, Xingguo Cui, Lianmei Zhang
  BMC Surgery.2024;[Epub]     CrossRef
• A Case of Intra-thyroidal Schwannoma Diagnosed by Preoperative Core Needle Biopsy
  Dong Gyu Choi, Young-Ok Kim, Min Jung Jung, Hyoung Shin Lee
  Korean Society for Head and Neck Oncology.2023; 39(1): 37.     CrossRef
• Multimodal ultrasound imaging of primary thyroid schwannoma
  Hai Na Zhao, Bu Yun Ma, Feng Yan, Yu Lan Peng
  Medicine.2021; 100(16): e25517.     CrossRef
• A Case of Anterior Cervical Intramuscular Schwannoma in the Strap Muscle
  Seul Gi Lee, Ho-Ryun Won, Bon Seok Koo, Jae Won Chang
  Korean Journal of Otorhinolaryngology-Head and Neck Surgery.2021; 64(4): 263.     CrossRef

Citations

Citations to this article as recorded by  

• Three-year delay in diagnosis of pulmonary sarcoidosis due to presence of necrotizing granulomas: a cautionary case report
  Yubing Yue, Rao Du, Ding Han, Tianxia Zhao, Chunfang Zeng, Yinhe Feng
  Frontiers in Medicine.2024;[Epub]     CrossRef
• Sarcoidosis With Skeletal Involvement Masquerading as Metastatic Malignancy
  Arthur M Samia, Stephanie Fabara Pino, Liang Sun
  Cureus.2023;[Epub]     CrossRef
• Necrotic sarcoid granulomatosis – a late stage of nodular sarcoidosis or an independent disease? Analysis of a clinical case
  E. A. Galushko, E. V. Pozhidaev, S. G. Radenska-Lopovok, A. V. Gordeev, M. V. Shaligina, A. V. Alekseeva, M. A. Sedelnikova
  Rheumatology Science and Practice.2023; 61(5): 624.     CrossRef
• Incidental Lung Cavity in the Heartland
  Biplab K. Saha, Om Dawani, Woon H Chong, Alyssa Bonnier
  The American Journal of the Medical Sciences.2022; 363(2): 191.     CrossRef
• A rare presentation of necrotizing sarcoidosis
  Nirali Sheth, Umaima Dhamrah, Branden Ireifej, David Song, Penpa Bhuti, Jagbir Singh, Henry Fan, Sibghatallah Ummar, Vikash Jaiswal, Nishan Babu Pokhrel
  Respirology Case Reports.2022;[Epub]     CrossRef
• Necrotizing Granulomatous Dacryoadenitis With Non-Necrotizing Granulomatous Scar Hypertrophy: Two Histological Variants of Sarcoidosis in the Same Patient
  Erin E. Godbout, M. Kristina Subik, Tal J. Rubinstein
  Ophthalmic Plastic & Reconstructive Surgery.2021; 37(1): e30.     CrossRef
• Necrotizing sarcoid granulomatosis simulating pulmonary malignancy
  Jun Hyeok Kim, Bo Da Nam, Jung Hwa Hwang, Dong Won Kim, Ki-Up Kim, Young Woo Park
  Medicine.2021; 100(49): e28208.     CrossRef
• Necrotizing Sarcoid Granulomatosis: A Disease Not to be Forgotten
  A. I. Parejo-Morón, M. L. Tornero-Divieso, M. R. Férnandez-Díaz, L. Muñoz-Medina, O. Preda, N. Ortego-Centeno
  Case Reports in Medicine.2020; 2020: 1.     CrossRef
• Clinical Reasoning: A woman with monocular vision loss
  Husain Danish, Tatiana Bakaeva, Isaac Solomon, Sashank Prasad
  Neurology.2020;[Epub]     CrossRef
• Cavity forms of thoracic sarcoidosis (literature review, clinical and radiological observations)
  A. V. Lenshin, A. V. Il'in, Yu. M. Perelman
  PULMONOLOGIYA.2020; 30(6): 831.     CrossRef
• Thoracic sarcoidosis versus tuberculosis: Need for a multi-disciplinary approach
  Agrima Mian, Animesh Ray
  Indian Journal of Radiology and Imaging.2018; 28(02): 267.     CrossRef
• Necrotizing sarcoid granulomatosis with clinical presentations of recurrent acute abdomen. Case report and literature review
  V. I. Vasilyev, S. G. Palshina, B. D. Chaltsev, S. G. Radenska-Lopovok, T. N. Safonova
  Terapevticheskii arkhiv.2017; 89(11): 60.     CrossRef

Citations

Citations to this article as recorded by  

• Warthin-like variant of papillary thyroid carcinoma with lymph node metastases: a case report and review of the literature
  Andrii Hryshchyshyn, Andrii Bahrii, Pavlina Botsun, Volodymyr Chuba
  Journal of Medical Case Reports.2024;[Epub]     CrossRef
• Warthin-like Papillary Thyroid Carcinoma: A Case Report and Review of the Literature
  J. N. Aparnna, Pavithra Ayyanar, Mukund N. Sable, Dillip Kumar Samal, Amit Kumar Adhya, Pritinanda Mishra
  International Journal of Surgical Pathology.2024;[Epub]     CrossRef
• Cytologic hallmarks and differential diagnosis of papillary thyroid carcinoma subtypes
  Agnes Stephanie Harahap, Chan Kwon Jung
  Journal of Pathology and Translational Medicine.2024; 58(6): 265.     CrossRef
• The Warthin-like variant of papillary thyroid carcinomas: a clinicopathologic analysis report of two cases
  Xing Zhao, Yijia Zhang, Pengyu Hao, Mingzhen Zhao, Xingbin Shen
  Oncologie.2023; 25(5): 581.     CrossRef
• Solid papillary thyroid carcinoma with Hashimoto’s thyroiditis: description of a further case with challenging cytological features
  Franco Fulciniti, Jessica Barizzi, Pierpaolo Trimboli, Luca Giovanella
  BMJ Case Reports.2019; 12(1): e226153.     CrossRef
• Preoperative Cytologic Diagnosis of Warthin-like Variant of Papillary Thyroid Carcinoma
  Jisup Kim, Beom Jin Lim, Soon Won Hong, Ju Yeon Pyo
  Journal of Pathology and Translational Medicine.2018; 52(2): 105.     CrossRef
• Warthin like papillary carcinoma - A rare variant of papillary carcinoma thyroid
  Mir Wajahat, Tazeen Jeelani, Kanika Gupta, Nusrat Bashir
  Human Pathology: Case Reports.2018; 13: 21.     CrossRef
• Cytological features of warthin‐like papillary thyroid carcinoma: A case report with review of previous cytology cases
  Archana George Vallonthaiel, Shipra Agarwal, Deepali Jain, Rajni Yadav, Nishikant A. Damle
  Diagnostic Cytopathology.2017; 45(9): 837.     CrossRef
• Comparison of EASYPREP® and SurePath® in thyroid fine‐needle aspiration
  Yosep Chong, Ki Hyun Baek, Jee Young Kim, Tae‐Jung Kim, Eun Jung Lee, Chang Suk Kang
  Diagnostic Cytopathology.2016; 44(4): 283.     CrossRef
• Ultrasonographic features and clinical characteristics of Warthin-like variant of papillary thyroid carcinoma
  Ga Ram Kim, Jung Hee Shin, Soo Yeon Hahn, Eun Young Ko, Young Lyun Oh
  Endocrine Journal.2016; 63(4): 329.     CrossRef
• Warthin-Like Papillary Thyroid Carcinoma Associated with Lymphadenopathy and Hashimoto’s Thyroiditis
  Karla Judith González-Colunga, Abelardo Loya-Solis, Luis Ángel Ceceñas-Falcón, Oralia Barboza-Quintana, René Rodríguez-Gutiérrez
  Case Reports in Endocrinology.2015; 2015: 1.     CrossRef
• Tumeur Warthin-like de la thyroïde : à propos d’un cas
  W. Rekik, A. Khadhar, A. Zehani, H. Azouz, I. Chelly, T. Ben Ghachem, A. Sellem, M. Tounsi, H. Ben Mahjouba, S. Haouet, N. Kchir
  Journal Africain du Cancer / African Journal of Cancer.2015; 7(4): 247.     CrossRef

Citations

Citations to this article as recorded by  

• Esophageal squamous cell carcinoma or high-grade dysplasia overlying leiomyoma, rare but not to be neglected
  Changyuan Guo, Dan Liu, Yong Liu, Lei Guo, Lulu Rong, Guiqi Wang, Ning Lu, Liyan Xue
  Esophagus.2021; 18(1): 125.     CrossRef
• Esophageal leiomyoma and simultaneous overlying squamous cell carcinoma: a case report and review of the literature
  Saadat Mehrabi, Mohammad Javad Yavari Barhaghtalab, Safoora Hejazinia, Hossein Saedi
  BMC Surgery.2021;[Epub]     CrossRef

Rearrangement of anaplastic lymphoma kinase (ALK) gene is the best predictor of response to crizotinib, an ALK tyrosine kinase inhibitor. However, the prevalence of the ALK fusion is low, so accurate patient identification is crucial for successful treatment using ALK inhibitors. Furthermore, most patients with lung cancer present with advanced-stage disease at the time of diagnosis, so it is important for pathologists to detect ALK-rearranged patients while effectively maximizing small biopsy or cytology specimens. In this review, we propose a guideline recommendation for ALK testing approved by the Cardiopulmonary Pathology Study Group of the Korean Society of Pathologists.

Citations

Citations to this article as recorded by  

• Molecular Characteristics of Radon Associated Lung Cancer Highlights MET Alterations
  Gabriele Gamerith, Marcel Kloppenburg, Finn Mildner, Arno Amann, Sabine Merkelbach-Bruse, Carina Heydt, Janna Siemanowski, Reinhard Buettner, Michael Fiegl, Claudia Manzl, Georg Pall
  Cancers.2022; 14(20): 5113.     CrossRef
• ALK Translocation in ALK-Positive Mesenchymal Tumors: Diagnostic and Therapeutic Insights
  Minsun Jung, Kyung Chul Moon, Jeongmo Bae, Tae Min Kim, Miso Kim, Yoon Kyung Jeon, Cheol Lee
  Archives of Pathology & Laboratory Medicine.2022; 146(12): 1460.     CrossRef
• Molecular biomarker testing for non–small cell lung cancer: consensus statement of the Korean Cardiopulmonary Pathology Study Group
  Sunhee Chang, Hyo Sup Shim, Tae Jung Kim, Yoon-La Choi, Wan Seop Kim, Dong Hoon Shin, Lucia Kim, Heae Surng Park, Geon Kook Lee, Chang Hun Lee
  Journal of Pathology and Translational Medicine.2021; 55(3): 181.     CrossRef
• Testing for EGFR Mutations and ALK Rearrangements in Advanced Non-Small-Cell Lung Cancer: Considerations for Countries in Emerging Markets
  Mercedes L Dalurzo, Alejandro Avilés-Salas, Fernando Augusto Soares, Yingyong Hou, Yuan Li, Anna Stroganova, Büge Öz, Arif Abdillah, Hui Wan, Yoon-La Choi
  OncoTargets and Therapy.2021; Volume 14: 4671.     CrossRef
• Molecular testing for advanced non-small cell lung cancer in Malaysia: Consensus statement from the College of Pathologists, Academy of Medicine Malaysia, the Malaysian Thoracic Society, and the Malaysian Oncological Society
  Pathmanathan Rajadurai, Phaik Leng Cheah, Soon Hin How, Chong Kin Liam, Muhammad Azrif Ahmad Annuar, Norhayati Omar, Noriah Othman, Nurhayati Mohd Marzuki, Yong Kek Pang, Ros Suzanna Ahmad Bustamam, Lye Mun Tho
  Lung Cancer.2019; 136: 65.     CrossRef
• Updated Molecular Testing Guideline for the Selection of Lung Cancer Patients for Treatment With Targeted Tyrosine Kinase Inhibitors
  Neal I. Lindeman, Philip T. Cagle, Dara L. Aisner, Maria E. Arcila, Mary Beth Beasley, Eric H. Bernicker, Carol Colasacco, Sanja Dacic, Fred R. Hirsch, Keith Kerr, David J. Kwiatkowski, Marc Ladanyi, Jan A. Nowak, Lynette Sholl, Robyn Temple-Smolkin, Benj
  Journal of Thoracic Oncology.2018; 13(3): 323.     CrossRef
• Updated Molecular Testing Guideline for the Selection of Lung Cancer Patients for Treatment With Targeted Tyrosine Kinase Inhibitors
  Neal I. Lindeman, Philip T. Cagle, Dara L. Aisner, Maria E. Arcila, Mary Beth Beasley, Eric H. Bernicker, Carol Colasacco, Sanja Dacic, Fred R. Hirsch, Keith Kerr, David J. Kwiatkowski, Marc Ladanyi, Jan A. Nowak, Lynette Sholl, Robyn Temple-Smolkin, Benj
  The Journal of Molecular Diagnostics.2018; 20(2): 129.     CrossRef
• Updated Molecular Testing Guideline for the Selection of Lung Cancer Patients for Treatment With Targeted Tyrosine Kinase Inhibitors: Guideline From the College of American Pathologists, the International Association for the Study of Lung Cancer, and the
  Neal I. Lindeman, Philip T. Cagle, Dara L. Aisner, Maria E. Arcila, Mary Beth Beasley, Eric H Bernicker, Carol Colasacco, Sanja Dacic, Fred R. Hirsch, Keith Kerr, David J. Kwiatkowski, Marc Ladanyi, Jan A. Nowak, Lynette Sholl, Robyn Temple-Smolkin, Benja
  Archives of Pathology & Laboratory Medicine.2018; 142(3): 321.     CrossRef
• 5′/ 3′ imbalance strategy to detect ALK fusion genes in circulating tumor RNA from patients with non-small cell lung cancer
  Yongqing Tong, Zhijun Zhao, Bei Liu, Anyu Bao, Hongyun Zheng, Jian Gu, Mary McGrath, Ying Xia, Bihua Tan, Chunhua Song, Yan Li
  Journal of Experimental & Clinical Cancer Research.2018;[Epub]     CrossRef
• Molecular testing and treatment patterns for patients with advanced non-small cell lung cancer: PIvOTAL observational study
  Dae Ho Lee, Ming-Sound Tsao, Karl-Otto Kambartel, Hiroshi Isobe, Ming-Shyan Huang, Carlos H. Barrios, Adnan Khattak, Filippo de Marinis, Smita Kothari, Ashwini Arunachalam, Xiting Cao, Thomas Burke, Amparo Valladares, Javier de Castro, Aamir Ahmad
  PLOS ONE.2018; 13(8): e0202865.     CrossRef
• Microfluidics-based immunofluorescence for fast staining of ALK in lung adenocarcinoma
  Saška Brajkovic, Benjamin Pelz, Maria-Giuseppina Procopio, Anne-Laure Leblond, Grégoire Repond, Ariane Schaub-Clerigué, Diego G Dupouy, Alex Soltermann
  Diagnostic Pathology.2018;[Epub]     CrossRef
• Expanded Circulating Tumor Cells from a Patient with ALK- Positive Lung Cancer Present with EML4-ALK Rearrangement Along with Resistance Mutation and Enable Drug Sensitivity Testing: A Case Study
  Zhuo Zhang, Hiroe Shiratsuchi, Nallasivam Palanisamy, Sunitha Nagrath, Nithya Ramnath
  Journal of Thoracic Oncology.2017; 12(2): 397.     CrossRef
• Molecular Testing of Lung Cancers
  Hyo Sup Shim, Yoon-La Choi, Lucia Kim, Sunhee Chang, Wan-Seop Kim, Mee Sook Roh, Tae-Jung Kim, Seung Yeon Ha, Jin-Haeng Chung, Se Jin Jang, Geon Kook Lee
  Journal of Pathology and Translational Medicine.2017; 51(3): 242.     CrossRef
• Novel ALK fusion partners in lung cancer
  Aglaya G. Iyevleva, Grigory A. Raskin, Vladislav I. Tiurin, Anna P. Sokolenko, Natalia V. Mitiushkina, Svetlana N. Aleksakhina, Aigul R. Garifullina, Tatiana N. Strelkova, Valery O. Merkulov, Alexandr O. Ivantsov, Ekatherina Sh. Kuligina, Kazimir M. Pozha
  Cancer Letters.2015; 362(1): 116.     CrossRef
• Strategic management of transthoracic needle aspirates for histological subtyping and EGFR testing in patients with peripheral lung cancer: An institutional experience
  Choonhee Son, Eun‐Ju Kang, Mee Sook Roh
  Diagnostic Cytopathology.2015; 43(7): 532.     CrossRef
• Current and future molecular diagnostics in non-small-cell lung cancer
  Chun Man Li, Wing Ying Chu, Di Lun Wong, Hin Fung Tsang, Nancy Bo Yin Tsui, Charles Ming Lok Chan, Vivian Wei Wen Xue, Parco Ming Fai Siu, Benjamin Yat Ming Yung, Lawrence Wing Chi Chan, Sze Chuen Cesar Wong
  Expert Review of Molecular Diagnostics.2015; 15(8): 1061.     CrossRef
• Role of biopsy sampling for diagnosis of early and progressed hepatocellular carcinoma
  Haeryoung Kim, Young Nyun Park
  Best Practice & Research Clinical Gastroenterology.2014; 28(5): 813.     CrossRef
• Molecular Pathology of Lung Cancer: Current Status and Future Directions
  Mee Sook Roh
  Tuberculosis and Respiratory Diseases.2014; 77(2): 49.     CrossRef
• Epidermal growth factor receptor mutations and anaplastic lymphoma kinase rearrangements in lung cancer with nodular ground-glass opacity
  Sung-Jun Ko, Yeon Joo Lee, Jong Sun Park, Young-Jae Cho, Ho Il Yoon, Jin-Haeng Chung, Tae Jung Kim, Kyung Won Lee, Kwhanmien Kim, Sanghoon Jheon, Hyojin Kim, Jae Ho Lee, Choon-Taek Lee
  BMC Cancer.2014;[Epub]     CrossRef