Author

Maria Samuel

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Asif Rasheed· 2 shared Abdulla al Shafi Majumder· 1 shared Abdullah Mesut ErzurumluogluiD· 1 shared Alex P. ReineriD· 1 shared Alison GoateiD· 1 shared Anders MälarstigiD· 1 shared Andrew C. HeathiD· 1 shared Andries R. van der Leij· 1 shared

Activity by Year

2015-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetics

Asif Rasheed

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Exome chip meta-analysis elucidates the genetic architecture of rare coding variants in smoking and drinking behavior

David M. Brazel, Yu Jiang, Jordan M. Hughey, Valérie Turcot, Xiaowei Zhan, Jian Gong, Chiara Batini, J. Dylan Weissenkampen, Mengzhen Liu, Daniel R. Barnes, Sarah E. Bertelsen, Yi‐Ling Chou, Abdullah Mesut Erzurumluoglu, Jessica D. Faul, Jeff Haessler, , Jean Ferrières

The paper analyzes rare coding variants in smoking and drinking behavior using exome chip data, finding that they contribute to phenotypic variation but require larger samples for individual variant associations.

Biological Psychiatry · Dec 6, 2018Peer-reviewedGenetics

Human knockouts in a cohort with a high rate of consanguinity

Danesh Saleheen, Pradeep Natarajan, Wei Zhao, Asif Rasheed, Sumeet Khetarpal, Hong-Hee Won, Konrad J Karczewski, Anne H ODonnell-Luria, Kaitlin E Samocha, Namrata Gupta, Mozzam Zaidi, Maria Samuel, Atif Imran, Shahid Abbas, Faisal Majeed, , Sekar Kathiresan

The paper identifies homozygous null mutations in 961 genes in a consanguineous Pakistani cohort and reports their phenotypic consequences.

bioRxiv · Nov 12, 2015Genomics