A citation-based method for searching scientific literature

Michael O Dorschner, Laura M Amendola, Emily H Turner, Peggy D Robertson, Brian H Shirts, Carlos J Gallego, Robin L Bennett, Kelly L Jones, Mari J Tokita, James T Bennett, Jerry H Kim, Elisabeth A Rosenthal, Daniel S Kim, Holly K Tabor, Michael J Bamshad, Arno G Motulsky, C Ronald Scott, Colin C Pritchard, Tom Walsh, Wylie Burke, Wendy H Raskind, Peter Byers, Fuki M Hisama, Deborah A Nickerson, Gail P Jarvik. Am J Hum Genet 2013
Times Cited: 270



Quan Li, Kai Wang. Am J Hum Genet 2017
Times Cited: 337




List of shared articles



Times cited

Estimation of the carrier frequencies and proportions of potential patients by detecting causative gene variants associated with autosomal recessive bone dysplasia using a whole-genome reference panel of Japanese individuals.
Shinichi Nagaoka, Yumi Yamaguchi-Kabata, Naomi Shiga, Masahito Tachibana, Jun Yasuda, Shu Tadaka, Gen Tamiya, Nobuo Fuse, Kengo Kinoshita, Shigeo Kure,[...]. Hum Genome Var 2021
0

Frequency and management of medically actionable incidental findings from genome and exome sequencing data: a systematic review.
Amal Elfatih, Idris Mohammed, Doua Abdelrahman, Borbala Mifsud. Physiol Genomics 2021
0

Frequency and spectrum of actionable pathogenic secondary findings in Taiwanese exomes.
Chieh-Wen Kuo, Wuh-Liang Hwu, Yin-Hsiu Chien, Ching Hsu, Miao-Zi Hung, I-Lin Lin, Feipei Lai, Ni-Chung Lee. Mol Genet Genomic Med 2020
3

CharGer: clinical Characterization of Germline variants.
Adam D Scott, Kuan-Lin Huang, Amila Weerasinghe, R Jay Mashl, Qingsong Gao, Fernanda Martins Rodrigues, Matthew A Wyczalkowski, Li Ding. Bioinformatics 2019
14

Estimating carrier frequencies of newborn screening disorders using a whole-genome reference panel of 3552 Japanese individuals.
Yumi Yamaguchi-Kabata, Jun Yasuda, Akira Uruno, Kazuro Shimokawa, Seizo Koshiba, Yoichi Suzuki, Nobuo Fuse, Hiroshi Kawame, Shu Tadaka, Masao Nagasaki,[...]. Hum Genet 2019
2

Inferring the effect of genomic variation in the new era of genomics.
Samya Chakravorty, Madhuri Hegde. Hum Mutat 2018
12