PASSIM - an open source software system for managing information in biomedical studies. - Juris Viksna; Edgars Celms; Martins Opmanis; Karlis Podnieks; Peteris Rucevskis; Andris Zarins; Amy Barrett; Sudeshna Guha Neogi; Maria Krestyaninova; Mark I. McCarthy; Alvis Brazma; Ugis Sarkans (BMC Bioinform., 2007)

A System for Information Management in BioMedical Studies - SIMBioMS. - Maria Krestyaninova; Andris Zarins; Juris Viksna; Natalja Kurbatova; Peteris Rucevskis; Sudeshna Guha Neogi; Mike Gostev; Teemu Perheentupa; Juha Knuuttila; Amy Barrett; Ilkka Lappalainen; Johan Rung; et al. (Bioinform., 2009)

SAIL - a software system for sample and phenotype availability across biobanks and cohorts. - Mikhail Gostev; Julio Fernandez-Banet; Johan Rung; Joern Dietrich; Inga Prokopenko; Samuli Ripatti; Mark I. McCarthy; Alvis Brazma; Maria Krestyaninova (Bioinform., 2011)

Assessing association between protein truncating variants and quantitative traits. - Manuel A. Rivas; Matti Pirinen; Matthew J. Neville; Kyle J. Gaulton; Loukas Moutsianas; Cecilia M. Lindgren; Fredrik Karpe; Mark I. McCarthy; Peter Donnelly (Bioinform., 2013)

Assessing allele-specific expression across multiple tissues from RNA-seq read data. - Matti Pirinen; Tuuli Lappalainen; Noah A. Zaitlen; Emmanouil T. Dermitzakis; Peter Donnelly; Mark I. McCarthy; Manuel A. Rivas (Bioinform., 2015)

The impact of rare variation on gene expression across tissues. - Xin Li 130; Yungil Kim; Emily K. Tsang; Joe R. Davis; Farhan N. Damani; Colby Chiang; Gaelen T. Hess; Zachary Zappala; Benjamin J. Strober; Alexandra J. Scott; Amy Li; Andrea Ganna; et al. (Nat., 2017)

Toppar: an interactive browser for viewing association study results. - Thorhildur Juliusdottir; Karina Banasik; Neil R. Robertson; Richard Mott; Mark I. McCarthy (Bioinform., 2018)

A structural variation reference for medical and population genetics. - Ryan L. Collins; Harrison Brand; Konrad J. Karczewski; Xuefang Zhao; Jessica Alföldi; Laurent C. Francioli; Amit V. Khera; Chelsea Lowther; Laura D. Gauthier; Harold Wang; Nicholas A. Watts; Matthew Solomonson; et al. (Nat., 2020)

Whole-genome sequencing of patients with rare diseases in a national health system. - Ernest Turro; William J. Astle; Karyn Megy; Stefan Gräf; Daniel Greene; Olga Shamardina; Hana Lango Allen; Alba Sanchis-Juan; Mattia Frontini; Chantal Thys; Jonathan Stephens; Rutendo Mapeta; et al. (Nat., 2020)