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Gabriel Haller

5PUBLICATIONS
38CO-AUTHORS
Infant and child healthAdolescent healthCardiovascular medicine and haematology not elsewhere classifiedOrthodontics and dentofacial orthopaedicsMolecular evolution
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Journal

Publications (5)

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|Feb 04, 2025
Using Artificial Intelligence to Identify Three Presenting Phenotypes of Chiari Type-1 Malformation and Syringomyelia.

Vivek Prakash Gupta, Ziqi Xu, Jacob K Greenberg

|Nov 22, 2021
Whole-exome analysis of adolescents with low VWF and heavy menstrual bleeding identifies novel genetic associations.

Brooke Sadler, Charles G Minard, Gabe Haller

|Feb 08, 2021
von Willebrand factor antigen levels are associated with burden of rare nonsynonymous variants in the VWF gene.

Brooke Sadler, Pamela A Christopherson, Gabe Haller

|May 22, 2020
<i>ATRAID</i> regulates the action of nitrogen-containing bisphosphonates on bone.

Lauren E Surface, Damon T Burrow, Jinmei Li

|Oct 04, 2016
Massively parallel single-nucleotide mutagenesis using reversibly terminated inosine.

Gabe Haller, David Alvarado, Kevin McCall

Pageof 1

Frequent Collaborators

2 joint publications

Brooke Sadler

1 joint publications

Lauren E Surface

1 joint publications

Damon T Burrow

1 joint publications

Jinmei Li

1 joint publications

Jiwoong Park

1 joint publications

Sandeep Kumar

1 joint publications

Cheng Lyu

1 joint publications

Niki Song

1 joint publications

Yangjin Bae

1 joint publications

Brendan H Lee

Frequent Collaborators

2 joint publications

Brooke Sadler

1 joint publications

Lauren E Surface

1 joint publications

Damon T Burrow

1 joint publications

Jinmei Li

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