A citation-based method for searching scientific literature

Karen A Cadoo, Diana L Mandelker, Semanti Mukherjee, Carolyn Stewart, Deborah DeLair, Vignesh Ravichandran, Preethi Srinivasan, Daire Hurley, Yelena Kemel, Angela G Arnold, Margaret Sheehan, Nisha Pradhan, Vijai Joseph, Dennis S Chi, Ginger J Gardner, Elizabeth L Jewell, Mario M Leitao, Kara Long Roche, Jennifer J Mueller, Yukio Sonoda, Oliver Zivanovic, Michael Walsh, Maria I Carlo, Michael F Berger, David Hyman, Liying Zhang, Mark E Robson, Kenneth Offit, Carol Aghajanian, Nadeem R Abu Rustum, Zsofia Stadler. JCO Precis Oncol 2019
Times Cited: 1







List of co-cited articles
articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Cystic fibrosis in Jews: frequency and mutation distribution.
B Kerem, O Chiba-Falek, E Kerem. Genet Test 1997
57
100


Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer.
Pengyuan Liu, Haris G Vikis, Daolong Wang, Yan Lu, Yian Wang, Ann G Schwartz, Susan M Pinney, Ping Yang, Mariza de Andrade, Gloria M Petersen,[...]. J Natl Cancer Inst 2008
113
100

Multi-Omics Analysis Reveals a HIF Network and Hub Gene EPAS1 Associated with Lung Adenocarcinoma.
Zhaoxi Wang, Yongyue Wei, Ruyang Zhang, Li Su, Stephanie M Gogarten, Geoffrey Liu, Paul Brennan, John K Field, James D McKay, Jolanta Lissowska,[...]. EBioMedicine 2018
20
100

Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development.
Yafang Li, Xiangjun Xiao, Yohan Bossé, Olga Gorlova, Ivan Gorlov, Younghun Han, Jinyoung Byun, Natasha Leighl, Jakob S Johansen, Matt Barnett,[...]. Oncotarget 2019
7
100

Fragments of ATM which have dominant-negative or complementing activity.
S E Morgan, C Lovly, T K Pandita, Y Shiloh, M B Kastan. Mol Cell Biol 1997
142
100

Fine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility loci.
Linda Kachuri, Christopher I Amos, James D McKay, Mattias Johansson, Paolo Vineis, H Bas Bueno-de-Mesquita, Marie-Christine Boutron-Ruault, Mikael Johansson, J Ramón Quirós, Sabina Sieri,[...]. Carcinogenesis 2016
27
100

Phevor combines multiple biomedical ontologies for accurate identification of disease-causing alleles in single individuals and small nuclear families.
Marc V Singleton, Stephen L Guthery, Karl V Voelkerding, Karin Chen, Brett Kennedy, Rebecca L Margraf, Jacob Durtschi, Karen Eilbeck, Martin G Reese, Lynn B Jorde,[...]. Am J Hum Genet 2014
100
100

A two-dimensional pooling strategy for rare variant detection on next-generation sequencing platforms.
Philip C Zuzarte, Robert E Denroche, Gordon Fehringer, Hagit Katzov-Eckert, Rayjean J Hung, John D McPherson. PLoS One 2014
10
100

A case-control study of a sex-specific association between a 15q25 variant and lung cancer risk.
Chongjuan Wei, Younghun Han, Margaret R Spitz, Xifeng Wu, Haidee Chancoco, Pinchas Akiva, Gideon Rechavi, Hadar Brand, Issac Wun, Marsha L Frazier,[...]. Cancer Epidemiol Biomarkers Prev 2011
11
100

Missense mutations but not allelic variants alter the function of ATM by dominant interference in patients with breast cancer.
Shaun P Scott, Regina Bendix, Philip Chen, Raymond Clark, Thilo Dork, Martin F Lavin. Proc Natl Acad Sci U S A 2002
113
100

Effects of ataxia telangiectasia mutated (ATM) genotypes and smoking habits on lung cancer risk in Taiwan.
Te-Chun Hsia, Chia-Wen Tsai, Shinn-Jye Liang, Wen-Shin Chang, Liang-Yi Lin, Wei-Chun Chen, Chih-Yen Tu, Chang-Hai Tsai, Da-Tian Bau. Anticancer Res 2013
25
100


Germline Mutations in DNA Repair Genes in Lung Adenocarcinoma.
Erin M Parry, Dustin L Gable, Susan E Stanley, Sara E Khalil, Valentin Antonescu, Liliana Florea, Mary Armanios. J Thorac Oncol 2017
29
100

Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics.
Linn Fagerberg, Björn M Hallström, Per Oksvold, Caroline Kampf, Dijana Djureinovic, Jacob Odeberg, Masato Habuka, Simin Tahmasebpoor, Angelika Danielsson, Karolina Edlund,[...]. Mol Cell Proteomics 2014
100

Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans.
H Krude, H Biebermann, W Luck, R Horn, G Brabant, A Grüters. Nat Genet 1998
100

Downregulation of hepatoma-derived growth factor contributes to retarded lung metastasis via inhibition of epithelial-mesenchymal transition by systemic POMC gene delivery in melanoma.
Han-En Tsai, Guei-Sheung Liu, Mei-Lang Kung, Li-Feng Liu, Jian-Ching Wu, Chia-Hua Tang, Ching-Hui Huang, San-Cher Chen, Hing-Chung Lam, Chieh-Shan Wu,[...]. Mol Cancer Ther 2013
21
100

Receptor for motilin identified in the human gastrointestinal system.
S D Feighner, C P Tan, K K McKee, O C Palyha, D L Hreniuk, S S Pong, C P Austin, D Figueroa, D MacNeil, M A Cascieri,[...]. Science 1999
276
100

Variants in motilin, somatostatin and their receptor genes and risk of biliary tract cancers and stones in Shanghai, China.
Hong-Li Xu, Ann W Hsing, Jill Koshiol, Lisa W Chu, Jia-Rong Cheng, Jing Gao, Yu-Ting Tan, Bing-Sheng Wang, Ming-Chang Shen, Yu-Tang Gao. Meta Gene 2014
6
100

A recurrent mutation in PARK2 is associated with familial lung cancer.
Donghai Xiong, Yian Wang, Elena Kupert, Claire Simpson, Susan M Pinney, Colette R Gaba, Diptasri Mandal, Ann G Schwartz, Ping Yang, Mariza de Andrade,[...]. Am J Hum Genet 2015
39
100

Transcriptome-wide association study reveals candidate causal genes for lung cancer.
Yohan Bossé, Zhonglin Li, Jun Xia, Venkata Manem, Robert Carreras-Torres, Aurélie Gabriel, Nathalie Gaudreault, Demetrius Albanes, Melinda C Aldrich, Angeline Andrew,[...]. Int J Cancer 2020
6
100

Performance comparison of benchtop high-throughput sequencing platforms.
Nicholas J Loman, Raju V Misra, Timothy J Dallman, Chrystala Constantinidou, Saheer E Gharbia, John Wain, Mark J Pallen. Nat Biotechnol 2012
786
100

Variants in nicotinic receptors and risk for nicotine dependence.
Laura Jean Bierut, Jerry A Stitzel, Jen C Wang, Anthony L Hinrichs, Richard A Grucza, Xiaoling Xuei, Nancy L Saccone, Scott F Saccone, Sarah Bertelsen, Louis Fox,[...]. Am J Psychiatry 2008
447
100

Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies.
Dalin Li, Juan Pablo Lewinger, William J Gauderman, Cassandra Elizabeth Murcray, David Conti. Genet Epidemiol 2011
93
100

Association of BRCA1 and BRCA2 mutations with survival, chemotherapy sensitivity, and gene mutator phenotype in patients with ovarian cancer.
Da Yang, Sofia Khan, Yan Sun, Kenneth Hess, Ilya Shmulevich, Anil K Sood, Wei Zhang. JAMA 2011
336
100

CHRNA5 risk variant predicts delayed smoking cessation and earlier lung cancer diagnosis--a meta-analysis.
Li-Shiun Chen, Rayjean J Hung, Timothy Baker, Amy Horton, Rob Culverhouse, Nancy Saccone, Iona Cheng, Bo Deng, Younghun Han, Helen M Hansen,[...]. J Natl Cancer Inst 2015
49
100

Neuroendocrine and epithelial phenotypes in small-cell lung cancer: implications for metastasis and survival in patients.
R Stovold, S L Meredith, J L Bryant, M Babur, K J Williams, E J Dean, C Dive, F H Blackhall, A White. Br J Cancer 2013
25
100

Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer.
Yanhong Liu, Christine M Lusk, Michael H Cho, Edwin K Silverman, Dandi Qiao, Ruyang Zhang, Michael E Scheurer, Farrah Kheradmand, David A Wheeler, Spiridon Tsavachidis,[...]. J Thorac Oncol 2018
10
100

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
James D McKay, Rayjean J Hung, Younghun Han, Xuchen Zong, Robert Carreras-Torres, David C Christiani, Neil E Caporaso, Mattias Johansson, Xiangjun Xiao, Yafang Li,[...]. Nat Genet 2017
175
100

The UK Biobank.
Paul M Matthews, Cathie Sudlow. Brain 2015
15
100



Increased risk of lung cancer in individuals with a family history of the disease: a pooled analysis from the International Lung Cancer Consortium.
Michele L Coté, Mei Liu, Stefano Bonassi, Monica Neri, Ann G Schwartz, David C Christiani, Margaret R Spitz, Joshua E Muscat, Gad Rennert, Katja K Aben,[...]. Eur J Cancer 2012
67
100

Leptin Modulates the Expression of miRNAs-Targeting POMC mRNA by the JAK2-STAT3 and PI3K-Akt Pathways.
Adel Derghal, Julien Astier, Flavie Sicard, Charlène Couturier, Jean-François Landrier, Lourdes Mounien. J Clin Med 2019
4
100

Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms.
Ivan P Gorlov, Olga Y Gorlova, Shamil R Sunyaev, Margaret R Spitz, Christopher I Amos. Am J Hum Genet 2008
236
100


Uncommon CHEK2 mis-sense variant and reduced risk of tobacco-related cancers: case control study.
Paul Brennan, James McKay, Lee Moore, David Zaridze, Anush Mukeria, Neonilia Szeszenia-Dabrowska, Jolanta Lissowska, Peter Rudnai, Eleonora Fabianova, Dana Mates,[...]. Hum Mol Genet 2007
54
100

Association analyses identify multiple new lung cancer susceptibility loci and their interactions with smoking in the Chinese population.
Jing Dong, Zhibin Hu, Chen Wu, Huan Guo, Baosen Zhou, Jiachun Lv, Daru Lu, Kexin Chen, Yongyong Shi, Minjie Chu,[...]. Nat Genet 2012
99
100

Systematic exploration of error sources in pyrosequencing flowgram data.
Susanne Balzer, Ketil Malde, Inge Jonassen. Bioinformatics 2011
65
100

Protein-altering germline mutations implicate novel genes related to lung cancer development.
Xuemei Ji, Semanti Mukherjee, Maria Teresa Landi, Yohan Bosse, Philippe Joubert, Dakai Zhu, Ivan Gorlov, Xiangjun Xiao, Younghun Han, Olga Gorlova,[...]. Nat Commun 2020
4
100

Comprehensive population screening in the Ashkenazi Jewish population for recurrent disease-causing variants.
L Shi, B D Webb, A H Birch, L Elkhoury, J McCarthy, X Cai, K Oishi, L Mehta, G A Diaz, L Edelmann,[...]. Clin Genet 2017
13
100

FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data.
Yafang Li, Jinyoung Byun, Guoshuai Cai, Xiangjun Xiao, Younghun Han, Olivier Cornelis, James E Dinulos, Joe Dennis, Douglas Easton, Ivan Gorlov,[...]. BMC Bioinformatics 2016
22
100


Neuropeptide receptor genes GHSR and NMUR1 are candidate epigenetic biomarkers and predictors for surgically treated patients with oropharyngeal cancer.
Kiyoshi Misawa, Masato Mima, Yamada Satoshi, Yuki Misawa, Atsushi Imai, Daiki Mochizuki, Takuya Nakagawa, Tomoya Kurokawa, Miki Oguro, Ryuji Ishikawa,[...]. Sci Rep 2020
10
100

Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.
Yufei Wang, James D McKay, Thorunn Rafnar, Zhaoming Wang, Maria N Timofeeva, Peter Broderick, Xuchen Zong, Marina Laplana, Yongyue Wei, Younghun Han,[...]. Nat Genet 2014
193
100

Differential analysis of mutations in the Jewish population and their implications for diseases.
Yaron Einhorn, Daphna Weissglas-Volkov, Shai Carmi, Harry Ostrer, Eitan Friedman, Noam Shomron. Genet Res (Camb) 2017
3
100

A Decade of GWAS Results in Lung Cancer.
Yohan Bossé, Christopher I Amos. Cancer Epidemiol Biomarkers Prev 2018
60
100

MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse.
Mieke Wesdorp, Silvia Murillo-Cuesta, Theo Peters, Adelaida M Celaya, Anne Oonk, Margit Schraders, Jaap Oostrik, Elena Gomez-Rosas, Andy J Beynon, Bas P Hartel,[...]. Am J Hum Genet 2018
18
100

MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss.
Guney Bademci, Clemer Abad, Armagan Incesulu, Abolfazl Rad, Ozgul Alper, Susanne M Kolb, Filiz B Cengiz, Oscar Diaz-Horta, Fatma Silan, Ercan Mihci,[...]. Hum Genet 2018
7
100

Current perspectives on CHEK2 mutations in breast cancer.
Panagiotis Apostolou, Ioannis Papasotiriou. Breast Cancer (Dove Med Press) 2017
38
100


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.