A citation-based method for searching scientific literature

Katherine S Pollard, Melissa J Hubisz, Kate R Rosenbloom, Adam Siepel. Genome Res 2010
Times Cited: 1252



Yongwook Choi, Gregory E Sims, Sean Murphy, Jason R Miller, Agnes P Chan. PLoS One 2012
Times Cited: 1781




List of shared articles



Times cited

A Homozygous Missense Variant in PPP1R1B/DARPP-32 Is Associated With Generalized Complex Dystonia.
Amjad Khan, Anne Molitor, Sylvain Mayeur, Gaoqun Zhang, Bruno Rinaldi, Béatrice Lannes, Benoît Lhermitte, Muhammad Umair, Stefan T Arold, Sylvie Friant,[...]. Mov Disord 2022
0

Analysis of missense variants in the human genome reveals widespread gene-specific clustering and improves prediction of pathogenicity.
Mathieu Quinodoz, Virginie G Peter, Katarina Cisarova, Beryl Royer-Bertrand, Peter D Stenson, David N Cooper, Sheila Unger, Andrea Superti-Furga, Carlo Rivolta. Am J Hum Genet 2022
2

A Compound Heterozygous Mutation in Calpain 1 Identifies a New Genetic Cause for Spinal Muscular Atrophy Type 4 (SMA4).
G Perez-Siles, M Ellis, A Ashe, B Grosz, S Vucic, M C Kiernan, K A Morris, S W Reddel, M L Kennerson. Front Genet 2022
0

DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing loss.
Fengxiao Bu, Mingjun Zhong, Qinyi Chen, Yumei Wang, Xia Zhao, Qian Zhang, Xiarong Li, Kevin T Booth, Hela Azaiez, Yu Lu,[...]. Hum Genet 2022
0

PHACT: Phylogeny-Aware Computing of Tolerance for Missense Mutations.
Nurdan Kuru, Onur Dereli, Emrah Akkoyun, Aylin Bircan, Oznur Tastan, Ogun Adebali. Mol Biol Evol 2022
0

Multiple primary malignances managed with surgical excision: a case report with next generation sequencing analysis.
Chiara Romano, Sandra Di Gregorio, Maria Stella Pennisi, Elena Tirrò, Giuseppe Broggi, Rosario Caltabiano, Livia Manzella, Martino Ruggieri, Paolo Vigneri, Antonio Di Cataldo. Mol Biol Rep 2022
0


Eph and Ephrin Variants in Malaysian Neural Tube Defect Families.
Siti Waheeda Mohd-Zin, Amelia Cheng Wei Tan, Wahib M Atroosh, Meow-Keong Thong, Abu Bakar Azizi, Nicholas D E Greene, Noraishah Mydin Abdul-Aziz. Genes (Basel) 2022
0

A novel variant in UBE3A in a family with multigenerational intellectual disability and developmental delay.
Xuechao Zhao, Yuting Zheng, Li Wang, Yanhong Wang, Shiyue Mei, Xiangdong Kong. Mol Genet Genomic Med 2022
1

Four novel candidate causal variants for deficient homozygous haplotypes in Holstein cattle.
Irene M Häfliger, Mirjam Spengeler, Franz R Seefried, Cord Drögemüller. Sci Rep 2022
0

Inherited and De Novo Variation in Lithuanian Genomes: Introduction to the Analysis of the Generational Shift.
Alina Urnikyte, Laura Pranckeniene, Ingrida Domarkiene, Svetlana Dauengauer-Kirliene, Alma Molyte, Ausra Matuleviciene, Ingrida Pilypiene, Vaidutis Kučinskas. Genes (Basel) 2022
0

Aggregated Genomic Data as Cohort-Specific Allelic Frequencies can Boost Variants and Genes Prioritization in Non-Solved Cases of Inherited Retinal Dystrophies.
Ionut-Florin Iancu, Irene Perea-Romero, Gonzalo Núñez-Moreno, Lorena de la Fuente, Raquel Romero, Almudena Ávila-Fernandez, María José Trujillo-Tiebas, Rosa Riveiro-Álvarez, Berta Almoguera, Inmaculada Martín-Mérida,[...]. Int J Mol Sci 2022
0

A comparison on predicting functional impact of genomic variants.
Dong Wang, Jie Li, Yadong Wang, Edwin Wang. NAR Genom Bioinform 2022
1

Computational Resources for the Interpretation of Variations in Cancer.
Grete Francesca Privitera, Salvatore Alaimo, Alfredo Ferro, Alfredo Pulvirenti. Adv Exp Med Biol 2022
0

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