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Author

Niki Mourtzi

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Galatea Bio (United States)ORCID 0000-0002-8650-4239Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2Approach:statistical model· 2Research Focus:gene regulatory network inference· 1Research Focus:GWAS / association mapping· 1Assay:whole-exome sequencing· 1Assay:whole-genome sequencing· 1

Frequent Co-Authors

Nicholas KatsanisiD· 2 sharedAlexander G. IoannidisiD· 1 sharedAlexandro J. MartagóniD· 1 sharedArturo López PinedaiD· 1 sharedAyşegül Ozantürk· 1 sharedAzita SadeghpouriD· 1 sharedBabak MoatamediD· 1 sharedCarlos D. BustamanteiD· 1 shared

Activity by Year

2020-2025 · peak 1/yr
012020: 1 paper (click to filter)1'202021: 0 papers'212022: 0 papers'222023: 0 papers'232024: 0 papers'242025: 1 paper (click to filter)1'25

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links
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MourtziNicholas Katsanis · 2 shared papersKatsanis · 2Alexander G. Ioannidis · 1 shared paperIoannidis · 1Alexandro J. Martagón · 1 shared paperMartagón · 1Arturo López Pineda · 1 shared paperPineda · 1Babak Moatamed · 1 shared paperMoatamed · 1Carlos D. Bustamante · 1 shared paperBustamante · 1Consuelo D. Quinto-Cortés · 1 shared paperQuinto-Cortés · 1Ayşegül Ozantürk · 1 shared paperOzantürk · 1Azita Sadeghpour · 1 shared paperSadeghpour · 1Christopher A. Cassa · 1 shared paperCassa · 1
Focal author (center)Selected co-authorORCID co-authorUnlinked name
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2 shared papersGenetic & Genomic Medicine
Nicholas KatsanisORCID

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2 papers

Recent·Most cited

Analysis of a deeply-phenotyped familial hypercholesterolemia cohort from Mexico shows a role for both rare and common alleles across known dyslipidemia genes and reveals structural variation in a novel locus.

Nicholas Katsanis, Niki Mourtzi, Consuelo D. Quinto-Cortés, Alexandro J. Martagón, Alexander G. Ioannidis, Francisco M. De La Vega, Jeff Gulcher, Ming Ta Michael Lee, Mohammad Ali Faghihi, Arturo López Pineda, Sonia Moreno–Grau, Daniel Mas Montserrat, Míriam Barrabés, David Bonet, Pavel Salazar Fernández, , Carlos D. Bustamante

The paper analyzes a Mexican FH cohort to show rare and common alleles in FH genes and a novel locus contribute to disease risk, with replication in UK Biobank.

Human Genomics · Nov 24, 2025Peer-reviewedGenetic & Genomic Medicine