A citation-based method for searching scientific literature

Y H Fu, D P Kuhl, A Pizzuti, M Pieretti, J S Sutcliffe, S Richards, A J Verkerk, J J Holden, R G Fenwick, S T Warren. Cell 1991
Times Cited: 1693



Peter K Todd, Seok Yoon Oh, Amy Krans, Fang He, Chantal Sellier, Michelle Frazer, Abigail J Renoux, Kai-chun Chen, K Matthew Scaglione, Venkatesha Basrur, Kojo Elenitoba-Johnson, Jean P Vonsattel, Elan D Louis, Michael A Sutton, J Paul Taylor, Ryan E Mills, Nicholas Charlet-Berguerand, Henry L Paulson. Neuron 2013
Times Cited: 283




List of shared articles



Times cited

Molecular mechanisms underlying nucleotide repeat expansion disorders.
Indranil Malik, Chase P Kelley, Eric T Wang, Peter K Todd. Nat Rev Mol Cell Biol 2021
0

FMR1 expression in human granulosa cells and variable ovarian response: control by epigenetic mechanisms.
Julia Rehnitz, Berthe Youness, Xuan Phuoc Nguyen, Jens E Dietrich, Sabine Roesner, Birgitta Messmer, Thomas Strowitzki, Peter H Vogt. Mol Hum Reprod 2021
1



Clustering of comorbid conditions among women who carry an FMR1 premutation.
Emily Graves Allen, Krista Charen, Heather S Hipp, Lisa Shubeck, Ashima Amin, Weiya He, Jessica Ezzell Hunter, Stephanie L Sherman. Genet Med 2020
9

Repeat expansion diseases.
Henry Paulson. Handb Clin Neurol 2018
101

FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohorts.
Claudine M Kraan, Quang M Bui, Mike Field, Alison D Archibald, Sylvia A Metcalfe, Louise M Christie, Bruce H Bennetts, Ralph Oertel, Melanie J Smith, Desiree du Sart,[...]. Genet Med 2018
12

Of Men and Mice: Modeling the Fragile X Syndrome.
Regina Dahlhaus. Front Mol Neurosci 2018
46