A citation-based method for searching scientific literature




Nilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, Sumit Middha, Shannon K McDonnell, Saurabh Baheti, Anthony Musolf, Qing Li, Emily Holzinger, Danielle Karyadi, Lisa A Cannon-Albright, Craig C Teerlink, Janet L Stanford, William B Isaacs, Jianfeng Xu, Kathleen A Cooney, Ethan M Lange, Johanna Schleutker, John D Carpten, Isaac J Powell, Olivier Cussenot, Geraldine Cancel-Tassin, Graham G Giles, Robert J MacInnis, Christiane Maier, Chih-Lin Hsieh, Fredrik Wiklund, William J Catalona, William D Foulkes, Diptasri Mandal, Rosalind A Eeles, Zsofia Kote-Jarai, Carlos D Bustamante, Daniel J Schaid, Trevor Hastie, Elaine A Ostrander, Joan E Bailey-Wilson, Predrag Radivojac, Stephen N Thibodeau, Alice S Whittemore, Weiva Sieh. Am J Hum Genet 2016
Times Cited: 709




List of shared articles



Times cited


SVPath: an accurate pipeline for predicting the pathogenicity of human exon structural variants.
Yaning Yang, Xiaoqi Wang, Deshan Zhou, Dong-Qing Wei, Shaoliang Peng. Brief Bioinform 2022
0

PPVED: A machine learning tool for predicting the effect of single amino acid substitution on protein function in plants.
Xiangjian Gou, Xuanjun Feng, Haoran Shi, Tingting Guo, Rongqian Xie, Yaxi Liu, Qi Wang, Hongxiang Li, Banglie Yang, Lixue Chen,[...]. Plant Biotechnol J 2022
2

Genome interpretation using in silico predictors of variant impact.
Panagiotis Katsonis, Kevin Wilhelm, Amanda Williams, Olivier Lichtarge. Hum Genet 2022
0

In silico identification of the rare-coding pathogenic mutations and structural modeling of human NNAT gene associated with anorexia nervosa.
Muhammad Bilal Azmi, Unaiza Naeem, Arisha Saleem, Areesha Jawed, Haroon Usman, Shamim Akhtar Qureshi, M Kamran Azim. Eat Weight Disord 2022
0


A Comprehensive Evaluation of the Performance of Prediction Algorithms on Clinically Relevant Missense Variants.
Erda Qorri, Bertalan Takács, Alexandra Gráf, Márton Zsolt Enyedi, Lajos Pintér, Ernő Kiss, Lajos Haracska. Int J Mol Sci 2022
0


Mannose binding lectin gene 2 (rs1800450) missense variant may contribute to development and severity of COVID-19 infection.
Alpay Medetalibeyoglu, Gulistan Bahat, Naci Senkal, Murat Kose, Kader Avci, Gozde Yesil Sayin, Ummuhan Isoglu-Alkac, Tufan Tukek, Sacide Pehlivan. Infect Genet Evol 2021
13

Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1.
Nahla N Abdel-Aziz, Ghada Y El-Kamah, Rabab A Khairat, Hanan R Mohamed, Yehia Z Gad, Akmal M El-Ghor, Khalda S Amr. Mol Genet Genomic Med 2021
1


MutTMPredictor: Robust and accurate cascade XGBoost classifier for prediction of mutations in transmembrane proteins.
Fang Ge, Yi-Heng Zhu, Jian Xu, Arif Muhammad, Jiangning Song, Dong-Jun Yu. Comput Struct Biotechnol J 2021
1


A novel ADAMTS17 variant that causes Weill-Marchesani syndrome 4 alters fibrillin-1 and collagen type I deposition in the extracellular matrix.
Stylianos Z Karoulias, Aude Beyens, Zerina Balic, Sofie Symoens, Anthony Vandersteen, Andrea L Rideout, John Dickinson, Bert Callewaert, Dirk Hubmacher. Matrix Biol 2020
22