Farhad Hormozdiari

19.2k citations

56 papers · 3.1k indexed · 2 hit papers · h-index 27

Co-authors: Eleazar Eskin Bogdan Paşaniuc Alkes L. Price Jong Wha J. Joo Eun Yong Kang Steven Gazal Ayellet V. Segrè Wen-Yun Yang
Topics: Genetic Associations and Epidemiology (27 papers)Genetic Mapping and Diversity in Plants and Animals (21 papers)Genomic variations and chromosomal abnormalities (11 papers)
Cited by: Genetics Molecular Biology Cancer Research
Journals: Nature Nucleic Acids Research Nature Communications
Partner nations: United States United Kingdom South Korea

In The Last Decade

Farhad Hormozdiari

55 papers receiving 3.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Colocalization of GWAS and eQTL Signals Detects Target Genes

2016 380 citations Farhad Hormozdiari, Martijn van de Bunt et al. The American Journal of Human Genetics profile →
Chromosome conformation elucidates regulatory relationships in developing human brain

2016 347 citations Hyejung Won, Luis de la Torre-Ubieta et al. Nature profile →

Peers

Countries citing papers authored by Farhad Hormozdiari

Since Specialization

Citations

This map shows the geographic impact of Farhad Hormozdiari's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Farhad Hormozdiari with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Farhad Hormozdiari more than expected).

Fields of papers citing papers by Farhad Hormozdiari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Farhad Hormozdiari. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Farhad Hormozdiari. The network helps show where Farhad Hormozdiari may publish in the future.

Co-authorship network of co-authors of Farhad Hormozdiari

This figure shows the co-authorship network connecting the top 25 collaborators of Farhad Hormozdiari. A scholar is included among the top collaborators of Farhad Hormozdiari based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Farhad Hormozdiari. Farhad Hormozdiari is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Applying multimodal AI to physiological waveforms improves genetic prediction of cardiovascular traits 2025 ·The American Journal of Human Genetics ·(unknown),(unknown),Taedong Yun,(unknown),Jacqueline Baras Shreibati,Dongbing Lai,Tae‐Hwi Schwantes‐An,Robert Luben,Zachary R. McCaw,Jorgen Engmann,Rui Providência,Amand F. Schmidt,Patricia B. Munroe,Howard H. Yang,Andrew Carroll,Anthony P. Khawaja,Cory Y. McLean,(unknown),Farhad Hormozdiari	0
2	Unsupervised representation learning on high-dimensional clinical data improves genomic discovery and prediction 2024 ·Nature Genetics ·Taedong Yun,(unknown),(unknown),Zachary R. McCaw,(unknown),Robert Luben,Dongbing Lai,John Bates,Howard H. Yang,Tae‐Hwi Schwantes‐An,(unknown),Anthony P. Khawaja,Andrew Carroll,Brian D. Hobbs,Michael H. Cho,Cory Y. McLean,Farhad Hormozdiari	13
3	Inference of chronic obstructive pulmonary disease with deep learning on raw spirograms identifies new genetic loci and improves risk models 2023 ·Nature Genetics ·(unknown),(unknown),Babak Alipanahi,Zachary R. McCaw,(unknown),Tae‐Hwi Schwantes‐An,Dongbing Lai,Andrew Carroll,Brian D. Hobbs,Michael H. Cho,Cory Y. McLean,Farhad Hormozdiari	25
4	Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity 2022 ·Nature Genetics ·Steven Gazal,Omer Weissbrod,Farhad Hormozdiari,Kushal K. Dey,Joseph Nasser,Karthik A. Jagadeesh,Daniel J. Weiner,Huwenbo Shi,Charles P. Fulco,Luke J. O’Connor,Bogdan Paşaniuc,J Engreitz,Alkes L. Price	73
5	Identifying causal variants by fine mapping across multiple studies 2021 ·PLoS Genetics ·Nathan LaPierre,(unknown),Helen J. Huang,(unknown),Farhad Hormozdiari,Eleazar Eskin	37
6	Annotations capturing cell type-specific TF binding explain a large fraction of disease heritability 2019 ·Human Molecular Genetics ·Bryce van de Geijn,Hilary K. Finucane,Steven Gazal,Farhad Hormozdiari,Tiffany Amariuta,Xuanyao Liu,Alexander Gusev,Po‐Ru Loh,Yakir Reshef,Gleb Kichaev,(unknown),Alkes L. Price	9
7	Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation 2018 ·Nature Genetics ·Eric R. Gamazon,Ayellet V. Segrè,Martijn van de Bunt,Xiaoquan Wen,Hualin Simon Xi,Farhad Hormozdiari,Halit Ongen,Anuar Konkashbaev,Eske M. Derks,François Aguet,Jie Quan,Dan L. Nicolae,Eleazar Eskin,Manolis Kellis,Gad Getz,Mark I. McCarthy,Emmanouil T. Dermitzakis,Nancy J. Cox,Kristin Ardlie	242
8	Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits 2018 ·Nature Genetics ·Farhad Hormozdiari,Steven Gazal,Bryce van de Geijn,Hilary K. Finucane,Chelsea J.‐T. Ju,Po‐Ru Loh,Armin Schoech,Yakir Reshef,Xuanyao Liu,Luke J. O’Connor,Alexander Gusev,Eleazar Eskin,Alkes L. Price	93
9	Widespread Allelic Heterogeneity in Complex Traits 2017 ·The American Journal of Human Genetics ·Farhad Hormozdiari,(unknown),Gleb Kichaev,Chelsea J.‐T. Ju,Ayellet V. Segrè,Jong Wha J. Joo,Hyejung Won,Sriram Sankararaman,Bogdan Paşaniuc,Sagiv Shifman,Eleazar Eskin	47
10	Hypothalamic transcriptomes of 99 mouse strains reveal trans eQTL hotspots, splicing QTLs and novel non-coding genes 2016 ·eLife ·Yehudit Hasin-Brumshtein,Arshad H. Khan,Farhad Hormozdiari,Calvin Pan,Brian W. Parks,Vladislav Petyuk,Paul Piehowski,Anneke Brümmer,Matteo Pellegrini,Xinshu Xiao,Eleazar Eskin,Richard Smith,Aldons J. Lusis,Desmond Smith	23
11	Imputing Phenotypes for Genome-wide Association Studies 2016 ·The American Journal of Human Genetics ·Farhad Hormozdiari,Eun Yong Kang,(unknown),Eyal Ben‐David,Chris D. Vulpe,Stela McLachlan,Aldons J. Lusis,Buhm Han,Eleazar Eskin	26
12	Multiple testing correction in linear mixed models 2016 ·Genome biology ·Jong Wha J. Joo,Farhad Hormozdiari,Buhm Han,Eleazar Eskin	48
13	Colocalization of GWAS and eQTL Signals Detects Target Genesbreakdown → 2016 ·The American Journal of Human Genetics ·Farhad Hormozdiari,Martijn van de Bunt,Ayellet V. Segrè,Xiao Li,Jong Wha J. Joo,(unknown),Jae Hoon Sul,Sriram Sankararaman,Bogdan Paşaniuc,Eleazar Eskin	380
14	Chromosome conformation elucidates regulatory relationships in developing human brainbreakdown → 2016 ·Nature ·Hyejung Won,Luis de la Torre-Ubieta,Jason L. Stein,Neelroop Parikshak,Jerry I. Huang,Carli K. Opland,Michael J. Gandal,Gavin J Sutton,Farhad Hormozdiari,Daning Lu,Chang‐Hoon Lee,Eleazar Eskin,Irina Voineagu,Jason Ernst,Daniel H. Geschwind	347
15	Integrating Functional Data to Prioritize Causal Variants in Statistical Fine-Mapping Studies 2014 ·PLoS Genetics ·Gleb Kichaev,Wen-Yun Yang,Sara Lindström,Farhad Hormozdiari,Eleazar Eskin,Alkes L. Price,Peter Kraft,Bogdan Paşaniuc	287
16	Identifying genetic relatives without compromising privacy 2014 ·Genome Research ·Dan He,Nicholas A. Furlotte,Farhad Hormozdiari,Jong Wha J. Joo,Akshay Wadia,Rafail Ostrovsky,Amit Sahai,Eleazar Eskin	28
17	Fast and accurate mapping of Complete Genomics reads 2014 ·Methods ·Donghyuk Lee,Farhad Hormozdiari,Hongyi Xin,Faraz Hach,Onur Mutlu,Can Alkan	5
18	Allele-specific expression and eQTL analysis in mouse adipose tissue 2014 ·BMC Genomics ·Yehudit Hasin-Brumshtein,Farhad Hormozdiari,Lisa Martin,Atila van Nas,Eleazar Eskin,Aldons J. Lusis,Thomas A. Drake	43
19	Assembly of non-unique insertion content using next-generation sequencing 2011 ·BMC Bioinformatics ·(unknown),Farhad Hormozdiari,Eleazar Eskin	21
20	Sensitive and fast mapping of di-base encoded reads 2011 ·Bioinformatics ·Farhad Hormozdiari,Faraz Hach,S. Cenk Şahinalp,Evan E. Eichler,Can Alkan	12

About Farhad Hormozdiari

Farhad Hormozdiari is a scholar working on Genetics, Molecular Biology and Cancer Research, having authored 56 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (27 papers), Genetic Mapping and Diversity in Plants and Animals (21 papers) and Genomic variations and chromosomal abnormalities (11 papers). The work is most often cited by research in Genetics (1.9k citations), Molecular Biology (1.8k citations) and Cancer Research (276 citations). Farhad Hormozdiari has collaborated with scholars based in United States, United Kingdom and South Korea. Frequent co-authors include Eleazar Eskin, Bogdan Paşaniuc, Alkes L. Price, Jong Wha J. Joo, Eun Yong Kang, Steven Gazal, Ayellet V. Segrè, Wen-Yun Yang, Emrah Kostem and Martijn van de Bunt. Their work appears in journals such as Nature, Nucleic Acids Research and Nature Communications.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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