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1
A Grading System for Resected Invasive Squamous Cell Carcinoma of the Lung: A Multi-Institutional Study by the IASLC Pathology Committee

von Mino-Kenudson, Mari ; Berezowska, Sabina ; Minami, Yuko ; et al.

In Journal of Thoracic Oncology February 2026 21(2):294-309
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2
Differentiating Separate Primary Lung Adenocarcinomas From Intrapulmonary Metastases With Emphasis on Pathological and Molecular Considerations: Recommendations From the International Association for the Study of Lung Cancer Pathology Committee

von Chou, Teh-Ying ; Dacic, Sanja ; Wistuba, Ignacio ; et al.

In Journal of Thoracic Oncology March 2025 20(3):311-330
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3
A prognostic model for use before elective surgery to estimate the risk of postoperative pulmonary complications (GSU-Pulmonary Score): a development and validation study in three international cohorts

von Bravo, Laura ; Simões, Joana FF ; Cardoso, Victor R ; et al.

In The Lancet Digital Health July 2024 6(7):e507-e519
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4
Polygenic prediction of body mass index and obesity through the life course and across ancestries

von Smit RAJ ; Wade KH ; Hui Q ; et al.

Schlagworte: Polygenic score; body mass index
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5
Demonstrating paths for unlocking the value of cloud genomics through cross cohort analysis

von Deflaux, N ; Selvaraj, MS ; Condon, HR ; et al.
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6
Automated patch clamp data improve variant classification and penetrance stratification for SCN5A–Brugada syndrome

von O’Neill, MJ ; Ma, JG ; Aldridge, JL ; et al.
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7
International Association for the Study of Lung Cancer Study of Reproducibility in Assessment of Pathologic Response in Resected Lung Cancers After Neoadjuvant Therapy

von Dacic, Sanja ; Travis, William ; Redman, Mary ; et al.

In Journal of Thoracic Oncology October 2023 18(10):1290-1302
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8
Thymic Carcinomas—A Concise Multidisciplinary Update on Recent Developments From the Thymic Carcinoma Working Group of the International Thymic Malignancy Interest Group

von Roden, Anja C. ; Ahmad, Usman ; Cardillo, Giuseppe ; et al.

In Journal of Thoracic Oncology May 2022 17(5):637-650
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9
Promise and Peril of a Genotype-First Approach to Mendelian Cardiovascular Disease.

von Asatryan, B ; Murray, B ; Tadros, R ; et al.

Schlagworte: biobank; cardiac arrhythmia; cardiomyopathy; genetics; precision health; precision medicine sudden cardiac death; Humans; Cardiovascular Diseases; Genetic Testing; Genetic Predisposition to Disease; Precision Medicine; Genotype; Risk Assessment; Phenotype
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10
The International Association for the Study of Lung Cancer Global Survey on Programmed Death-Ligand 1 Testing for NSCLC

von Mino-Kenudson, Mari ; Le Stang, Nolwenn ; Daigneault, Jillian B. ; et al.

In Journal of Thoracic Oncology April 2021 16(4):686-696
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11
EURACAN/IASLC Proposals for Updating the Histologic Classification of Pleural Mesothelioma: Towards a More Multidisciplinary Approach

von Nicholson, Andrew G. ; Sauter, Jennifer L. ; Nowak, Anna K. ; et al.

In Journal of Thoracic Oncology January 2020 15(1):29-49
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12
Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets

von Haas, KM ; McGregor, MJ ; Bouhaddou, M ; et al.

Schlagworte: England
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13
Pathologic Considerations and Standardization in Mesothelioma Clinical Trials

von Tsao, Ming-Sound ; Carbone, Michele ; Galateau-Salle, Francoise ; et al.

In Journal of Thoracic Oncology October 2019 14(10):1704-1717
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14
Best Practices Recommendations for Diagnostic Immunohistochemistry in Lung Cancer

von Yatabe, Yasushi ; Dacic, Sanja ; Borczuk, Alain C. ; et al.

In Journal of Thoracic Oncology March 2019 14(3):377-407
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15
Rare variation in drug metabolism and Long QT genes and the genetic susceptibility to acquired Long QT syndrome

von Gray, B ; Baruteau, AE ; Antolin, AA ; et al.
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16
A Saturated Map of Common Genetic Variants Associated with Human Height

von Yengo, Loïc ; Vedantam, Sailaja ; Miao, Jenkai ; et al.

Schlagworte: common single-nucleotide polymorphisms (SNPs); human height; genome; ancestry
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17
A saturated map of common genetic variants associated with human height.

von Yengo, L ; Vedantam, S ; Marouli, E ; et al.
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18
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.

von Walsh, R ; Lahrouchi, N ; Tadros, R ; et al.
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19
Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome

von Lahrouchi N ; Tadros R ; Crotti L ; et al.

Schlagworte: genome-wide association study; inheritance pattern; long QT syndrome; Settore BIOS-14/A - Genetica; Settore MEDS-24/A - Statistica medica; Settore MEDS-07/B - Malattie dell'apparato cardiovascolare
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20
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition

von Roberts JD ; Asaki SY ; Mazzanti A ; et al.

Schlagworte: arrhythmia; genetic; long QT syndrome; penetrance; sudden cardiac death; Settore BIOS-14/A - Genetica; Settore MEDS-07/B - Malattie dell'apparato cardiovascolare
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21
Genome-wide study identifies association between HLA-B∗55:01 and self-reported penicillin allergy

von Krebs, K ; Bovijn, J ; Zheng, N ; et al.
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22
Understanding the use of observational and randomized data in cardiovascular medicine

von Bowman, L ; Baras, A ; Bombien, R ; et al.
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23
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

von Walsh, R ; Lahrouchi, N ; Tadros, R ; et al.

Genetics in Medicine (2020) (In press).

Schlagworte: variant interpretation; LQTS; Brugada; ACMG/AMP guidelines
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24
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

von Ntalla, I ; Weng, L-C ; Cartwright, JH ; et al.

Nature Communications , 11 (1) , Article 2542. (2020)

Schlagworte: Cardiovascular diseases; Cardiovascular genetics; Genome-wide association studies
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25
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition

von Roberts, JD ; Asaki, SY ; Mazzanti, A ; et al.

Circulation , 141 (6) pp. 429-439. (2020)

Schlagworte: Arrhythmia; genetics; long QT syndrome; penetrance; sudden cardiac death
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