Publications:

Multivariate Genome-wide Association Analysis by Iterative Hard Thresholding.

Bioinformatics (Oxford, England)

Chu, Benjamin B BB; Ko, Seyoon S; Zhou, Jin J JJ; Jensen, Aubrey A; Zhou, Hua H; Sinsheimer, Janet S JS; Lange, Kenneth K

Publication Date: 2023-04-17

Variant appearance in text: rs77870048

PubMed Link: 37067496

Variant Present in the following documents:

• Main text
• btad193_supplementary_data.pdf
• btad193.pdf

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Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports

Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-10-14

Variant appearance in text: rs77870048

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2

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Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities.

Nature Communications

Francis, Catherine M CM; Futschik, Matthias E ME; Huang, Jian J; Bai, Wenjia W; Sargurupremraj, Muralidharan M; Teumer, Alexander A; Breteler, Monique M B MMB; Petretto, Enrico E; Ho, Amanda S R ASR; Amouyel, Philippe P; Engelter, Stefan T ST; Bülow, Robin R; Völker, Uwe U; Völzke, Henry H; Dörr, Marcus M; Imtiaz, Mohammed-Aslam MA; Aziz, N Ahmad NA; Lohner, Valerie V; Ware, James S JS; Debette, Stephanie S; Elliott, Paul P; Dehghan, Abbas A; Matthews, Paul M PM

Publication Date: 2022-08-03

Variant appearance in text: rs77870048

PubMed Link: 35922433

Variant Present in the following documents:

• Main text

View BVdb publication page