John Blangero

University of Texas Rio Grande Valley School of Medicine

H指数:120

被引数:7.4万

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个人简介

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教育背景

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工作经历

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荣誉奖项

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Transcriptomic Architecture of Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) Risk in Mexican Americans

墨西哥裔美国人代谢功能障碍相关脂肪性肝病（MASLD）风险的转录组架构

Cells

IF5.2

2026-09-020

Association of Ultra-Processed Food Intake with Insulin Secretion and Sensitivity in Mexican American Children: Results from the SAFARI Study

墨西哥裔美国儿童超加工食品摄入与胰岛素分泌及敏感性的关联：SAFARI研究的结果

Nutrients

IF5

2026-08-110

OAAI

Integration of lipidomic and polygenic risk scores within contemporary clinical cardiovascular risk assessment pathways: a multi-cohort development and validation study

脂质组学和多基因风险评分在当代临床心血管风险评估路径中的整合：一项多队列开发与验证研究

EClinicalMedicine

IF10

2026-08-010

OAAI

Dakic, Aleksandar; Wu, Jingqin; Wang, Tingting; Meikle, Thomas G.; Huynh, Kevin; Yi, Changyu; Beyene, Habtamu B.; Salim, Agus; Cinel, Michelle; Mellett, Nat; Duong, Thy; Faulkner, Alexandra N.; van Buuren-Milne, Matilda; Bhagwat, Anjali; Shaw, Jonathan E.; Magliano, Dianna J.; Watts, Gerald F.; Hung, Joseph; Hui, Jennie; Beilby, John P.; Blangero, John; Moses, Eric K.; Southey, Melissa C.; Milne, Roger L.; Hodge, Allison M.; McNeil, John J.; Lacaze, Paul; Yu, Chenglong; Wolfe, Rory; Yang, Jean YH.; Grieve, Stuart M.; Chow, Clara K.; Vernon, Stephen T.; Gray, Michael P.; Figtree, Gemma A.; Morton, Jedidiah I.; Scuffham, Paul; Woodward, Mark; Kalman, Lisa; Paige, Ellie; Carrington, Melinda J.; Inouye, Michael; Giles, Corey; Meikle, Peter J.

Translational animal model for genetic predisposition to anophthalmia/ microphthalmia

遗传性无眼/小眼症的动物模型研究

Experimental Eye Research

IF2.7

2026-06-010

PRE

Cross-Sectional Associations of Metabolically Healthy Obesity, Lifestyle Factors, and Steatotic Liver Disease in Adults from the Fels Longitudinal Study

代谢健康型肥胖、生活方式因素与Fels纵向研究中成人脂肪性肝病的横断面关联

Metabolites

IF3.7

2026-04-280

OAAI

Genetic Variants and Molecular Components Associated with Metabolic Dysfunctional-Associated Steatotic Liver Disease and Depression: Shared Association of ADAMTS7 and THRAP3

与代谢功能障碍相关脂肪性肝病和抑郁症相关的遗传变异及分子组分：ADAMTS7和THRAP3的共享关联

Genes

IF2.8

2026-04-060

OAAI

cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions

cellSTAAR：整合基于单细胞测序的功能数据，以提升非编码区域稀有变异关联检验的功效

Nature Methods

IF32.1

2025-12-310

PRE

Eric Van Buren; Yi Zhang; Xihao Li; Margaret Sunitha Selvaraj; Zilin Li; Hufeng Zhou; Nicholette D. Palmer; Donna K. Arnett; John Blangero; Eric Boerwinkle; Brian E. Cade; Jenna C. Carlson; April P. Carson; Yii-Der Ida Chen; Joanne Curran; Ravindranath Duggirala; Myriam Fornage; Nora Franceschini; Misa Graff; Charles Gu; Xiuqing Guo; Jiang He; Nancy Heard-Cosa; Lifang Hou; Yi-Jen Hung; Rita R. Kalyani; Sharon L. R. Kardia; Eimear Kenny; Charles Kooperberg; Brian G. Kral; Leslie Lange; Dan Levy; Changwei Li; Simin Liu; Donald Lloyd-Jones; Ruth J. F. Loos; Ani W. Manichaikul; Lisa Warsinger Martin; Rasika Mathias; Ryan L. Minster; Braxton D. Mitchell; Josyf C. Mychaleckyj; Take Naseri; Kari North; Jeff O’Connell; James A. Perry; Patricia A. Peyser; Bruce M. Psaty; Laura M. Raffield; Ramachandran S. Vasan; Susan Redline; Alex P. Reiner; Stephen S. Rich; Jennifer A. Smith; Brian Spitzer; Hua Tang; Kent D. Taylor; Russell Tracy; Satupa’itea Viali; Lisa Yanek; Wei Zhao; Jerome I. Rotter; Gina M. Peloso; Pradeep Natarajan; Xihong Lin

Genome-wide association study identifies novel variants in olfactory, vitamin A, vitamin B, and cadherin pathways associated with learning and memory

全基因组关联研究鉴定出与学习记忆相关的嗅觉、维生素A、维生素B和钙黏蛋白通路的新型变异。

Scientific Reports

IF3.9

2025-12-180

OAAI

Role of epigenetic markers in cardiovascular disease following hypertensive disorders of pregnancy

妊娠期高血压疾病后表观遗传标记物在心血管疾病中的作用

Epigenomics

IF2.6

2025-10-080

PRE

Correction: A scan of pleiotropic immune mediated disease genes identifies novel determinants of baseline FVIII inhibitor status in hemophilia A

更正：对多效性免疫介导疾病基因的扫描识别出血友病A中基线FVIII抑制剂状态的新的决定因素

Genes & Immunity

IF0

2025-09-250

PREAI

Marcio A. Almeida; Vincent P. Diego; Kevin R. Viel; Bernadette W. Luu; Karin Haack; Raja Rajalingam; Afshin Ameri; Meera Chitlur; Natalia Rydz; David Lillicrap; Raymond G. Watts; Craig M. Kessler; Christopher Ramsey; Long V. Dinh; Benjamin Kim; Jerry S. Powell; Eron G. Manusov; Juan M. Peralta; Ruayda Bouls; Shirley M. Abraham; Yu-Min Shen; Carlos M. Murillo; Henry Mead; Paul V. Lehmann; Eli J. Fine; Miguel A. Escobar; Satish Kumar; Barbara A. Konkle; Sarah Williams-Blangero; Carol K. Kasper; Laura Almasy; Shelley A. Cole; John Blangero; Tom E. Howard

Association of genetic scores related to insulin resistance with neurological outcomes in ancestrally diverse cohorts from the Trans-Omics for Precision Medicine (TOPMed) program

与胰岛素抵抗相关的遗传评分与 ancestry 多样化队列中神经病学结局的关联：来自精准医学跨组学计划 (TOPMed) 的数据

Communications Biology

IF5.1

2025-09-240

OAAI

Chloé Sarnowski; Yixin Zhang; Farah Ammous; Lincoln M. P. Shade; Daniel DiCorpo; Xueqiu Jian; Donna K. Arnett; Thomas R. Austin; Alexa Beiser; Joshua C. Bis; John Blangero; Eric Boerwinkle; Jan Bressler; Joanne E. Curran; Charles S. DeCarli; Harsha Doddapaneni; Josée Dupuis; David W. Fardo; Jose C. Florez; Stacey Gabriel; Richard A. Gibbs; David C. Glahn; Namrata Gupta; Hector M. González; Kevin A. González; Konstantinos Hatzikotoulas; Kathleen M. Hayden; Susan R. Heckbert; Bertha Hidalgo; Alicia Huerta-Chagoya; Timothy M. Hughes; Sharon L. R. Kardia; Charles L. Kooperberg; Lenore J. Launer; W. T. Longstreth; Ravi Mandla; Rasika A. Mathias; Andrew P. Morris; Thomas H. Mosley; Ilya M. Nasrallah; Paul Nyquist; Bruce M. Psaty; Qibin Qi; Laura M. Raffield; Nigel W. Rayner; Alexander P. Reiner; Claudia L. Satizabal; Elizabeth Selvin; Magdalena D. R. Sevilla-Gonzalez; Albert V. Smith; Jennifer A. Smith; Kirk Smith; Beverly M. Snively; Lorraine Southam; Tamar Sofer; Ken Suzuki; Henry J. Taylor; Miriam S. Udler; Karine A. Viaud-Martinez; Sylvia Wassertheil-Smoller; Alexis C. Wood; Lisa R. Yanek; Xianyong Yin; Alisa K. Manning; Jerome I. Rotter; Stephen S. Rich; James B. Meigs; Myriam Fornage; Sudha Seshadri; Alanna C. Morrison

Penetrance of neurodevelopmental copy number variants is associated with variations in cortical morphology

神经发育性拷贝数变异的穿透性与皮层形态变异相关

biological psychiatry cognitive neuroscience and neuroimaging

IF0

2025-05-230

PREAI

Ana I. Silva; Ida E. Sønderby; George Kirov; Abdel Abdellaoui; Ingrid Agartz; David Ames; Nicola J. Armstrong; Eric Artiges; Tobias Banaschewski; Anne S. Bassett; Carrie E. Bearden; John Blangero; Rune Boen; Dorret I. Boomsma; Robin Bülow; Nancy J. Butcher; Vince Calhoun; Linda E. Campbell; Eva W.C. Chow; Simone Ciufolini; Michael C. Craig; Benedicto Crespo-Farroco; Adam C. Cunningham; Shareefa Dalvie; Eileen Daly; Paola Dazzan; Eco J.C. de Geus; Greig I. de Zubicaray; Joanne L. Doherty; Gary Donohoe; Mark Drakesmith; Thomas Espeseth; Vincent Frouin; Hugh Garavan; David C. Glahn; Naomi J. Goodrich-Hunsaker; Penny A. Gowland; Hans J. Grabe; Antoine Grigis; Maria Gudbrandsen; Boris A. Gutman; Jan Haavik; Asta K. Håberg; Jeremy Hall; Andreas Heinz; Sarah Hohmann; Jouke-Jan Hottenga; Sébastien Jacquemont; Neda Jahanshad; Rachel K. Jonas; Derek K. Jones; Erik G. Jönsson; Sanne Koops; Kuldeep Kumar; Stephanie Le Hellard; Herve Lemaitre; Jingyu Liu; Astri J. Lundervold; Jean-Luc Martinot; Karen A. Mather; Donna M. McDonald-McGinn; Katie L. McMahon; Allan F. McRae; Sarah E. Medland; Clara A. Moreau; Kieran C. Murphy; Declan Murphy; Robin M. Murray; Frauke Nees; Michael J. Owen; Marie-Laure Paillère Martinot; Diimitri Papadopoulos Orfanos; Tomas Paus; Luise Poustka; Tiago Reis Marques; David R. Roalf; Perminder S. Sachdev; Freda Scheffler; J. Eric Schmitt; Gunter Schumann; Vidar M. Steen; Dan J. Stein; Lachlan T. Strike; Alexander Teumer; Anbupalam Thalamuthu; Sophia I. Thomopoulos; Diana Tordesillas-Gutiérrez; Julian N. Trollor; Anne Uhlmann; Ariana Vajdi; Dennis van ’t Ent; Therese van Amelsvoort; Marianne B.M. van den Bree; Dennis van der Meer; Javier Vázquez-Bourgon; Julio E. Villalón-Reina; Uwe Völker; Henry Völzke; Jacob A.S. Vorstman; Lars T. Westlye; Nigel Williams; Katharina Wittfeld; Margaret J. Wright; Paul M. Thompson; Ole A. Andreassen; David E.J. Linden

Endophenotype-Informed Association Analyses for Liver Fat Accumulation and Metabolic Dysfunction in the Fels Longitudinal Study

基于内表型信息的肝脏脂肪积累和代谢功能障碍的关联分析：Fels纵向研究

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

IF4.9

2025-05-170

Genetic study of von Willebrand factor antigen levels ≤ 50 IU/dL identifies variants associated with increased risk of von Willebrand disease and bleeding

von Willebrand因子抗原水平≤50 IU/dL的遗传学研究确定了与血管性血友病和出血风险增加相关的变异。

Journal of Thrombosis and Haemostasis

IF5

2025-05-120

PRE

Rachel K. Friedman; Adam S. Heath; Jennifer E. Huffman; James T. Baker; Natalie R. Hasbani; Sarah A. Gagliano Taliun; Ming–Huei Chen; Tom E. Howard; Joshua P. Lewis; Nathan Pankratz; Snehal Patil; Alex P. Reiner; Florian Thibord; Lisa R. Yanek; Jie Yao; Hung–Hsin Chen; Joanne E. Curran; Nauder Faraday; Xiuqing Guo; Marsha M. Wheeler; Kathleen A. Ryan; Xiang Zhou; Kelly Cho; Laura Almasy; Paul L. Auer; Lewis C. Becker; Peter W.F. Wilson; Eric Boerwinkle; Jeffrey R. O’Connell; Stephen S. Rich; David C. Samuels; John Blangero; Myriam Fornage; Charles Kooperberg; Rasika A. Mathias; Braxton D. Mitchell; Jerome I. Rotter; Andrew D. Johnson; Nicholas L. Smith; Zeynep H. Coban–Akdemir; Jennifer E. Below; Alanna C. Morrison; Jill M. Johnsen; Paul S. de Vries

Thalamocortical Structural Covariation Networks Are Related to Familial Risk for Schizophrenia in the Context of Lower Nuclei Volume Estimates in Patients: An ENIGMA Study

丘脑皮层结构共变网络与精神分裂症家族风险相关：基于患者核体积估计值较低背景下的ENIGMA研究

Biological Psychiatry

IF9

2025-05-080

OAAI

Annalisa Lella; Linda A. Antonucci; Roberta Passiatore; Loredana Bellantuono; Pierluigi Selvaggi; Teresa Popolizio; Guido Di Sciascio; Alessandro Saponaro; Patrizia Ricci; Mario Altamura; Giuseppe Blasi; Antonio Rampino; Chris Vriend; Vince D. Calhoun; Kelly Rootes-Murdy; Aaron L. Goldman; Inmaculada Baeza; Josefina Castro-Fornieles; Gisela Sugranyes; Elena De la Serna; Edith Pomarol-Clotet; Mar Fatjó-Vilas; Raymond Salvador; Andriana Karuk; Paola Fuentes-Claramonte; David C. Glahn; Amanda L. Rodrigue; John Blangero; Lei Wang; Taeyoung Lee; Karolin E. Einenkel; Saskia Hamers; Oliver Gruber; Adrian Preda; Young-Chul Chung; Soyolsaikhan Odkhuu; Corentin Vallée; Paola Dazzan; Machteld Marcelis; Stijn Michielse; Katharina Brosch; Frederike Stein; Igor Nenadić; Benjamin Straube; Florian Thomas-Odenthal; Tilo Kircher; Sean Carruthers; Susan L. Rossell; Phillip J. Sumner; Tamsyn E. Van Rheenen; Caroline Demro; Ian S. Ramsay; Scott R. Sponheim; Rebekka Lencer; Susanne Meinert; Tim Hahn; Udo Dannlowski; Dominik Grotegerd; Mariateresa Ciccarelli; Felice Iasevoli; Giuseppe Pontillo; Godfrey D. Pearlson; Derin Cobia; Fabrizio Piras; Nerisa Banaj; Daniela Vecchio; Marjolein E.A. Barendse; Neeltje E.M. van Haren; Hang Joon Jo; Kang Sim; Yann Quidé; Melissa J. Green; Rachael Slate; Giacomo Cecere; Wolfgang Omlor; Stephanie Homan; Philipp Homan; Sophia I. Thomopoulos; Jessica A. Turner; Theo G.M. van Erp; Paul M. Thompson; Alessandro Bertolino; Giulio Pergola

Lifespan reference curves for harmonizing multi-site regional brain white matter metrics from diffusion MRI

多站点扩散MRI区域性脑白质指标调和的生命期参考曲线

SCIENTIFIC DATA

IF6.9

2025-05-061

Statin effects on the lipidome: Predicting statin usage and implications for cardiovascular risk prediction

他汀类药物对脂质组的影响：预测他汀类药物使用及其对心血管风险预测的启示

JOURNAL OF LIPID RESEARCH

IF4.1

2025-05-010

OAAI

A scan of pleiotropic immune mediated disease genes identifies novel determinants of baseline FVIII inhibitor status in hemophilia A

对多效性免疫介导疾病基因的扫描识别出血友病A中基础FVIII抑制剂状态的新的决定因素

GENES AND IMMUNITY

IF4.5

2025-04-220

PRE

Almeida, Marcio A.; Diego, Vincent P.; Viel, Kevin R.; Luu, Bernadette W.; Haack, Karin; Raja, Rajalingam; Ameri, Afshin; Chitlur, Meera; Rydz, Natalia; Lillicrap, David; Watts, Raymond G.; Kessler, Craig M.; Ramsey, Christopher; Dinh, Long V.; Kim, Benjamin; Powell, Jerry S.; Manusov, Eron G.; Peralta, Juan M.; Bouls, Ruayda; Abraham, Shirley M.; Shen, Yu-Min; Murillo, Carlos M.; Mead, Henry; Lehmann, Paul V.; Fine, Eli J.; Escobar, Miguel A.; Kumar, Satish; Konkle, Barbara A.; Williams-Blangero, Sarah; Kasper, Carol K.; Almasy, Laura; Cole, Shelley A.; Blangero, John; Howard, Tom E.

Disentangling effects of the DR and DQ isomers encoded by the HLA class II haplotype DRB1*15:01/DQB1*06:02 to help establish the true risk allele for FVIII inhibitor development in Hemophilia A

区分由HLA-II类单倍型DRB1*15:01/DQB1*06:02编码的DR和DQ异构体的效应，以帮助确定血友病A中FVIII抑制剂发展的真实风险等位基因。

FRONTIERS IN GENETICS

IF2.8

2025-04-090

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk

罕见的有害CCR2变异与较低的生命周期心血管风险相关

GENOME MEDICINE

IF11.2

2025-03-211

Georgakis, Marios K.; Malik, Rainer; Bounkari, Omar El; Hasbani, Natalie R.; Li, Jiang; Huffman, Jennifer E.; Shakt, Gabrielle; Tack, Reinier W. P.; Kimball, Tamara N.; Asare, Yaw; Morrison, Alanna C.; Tsao, Noah L.; Judy, Renae; Mitchell, Braxton D.; Xu, Huichun; Montasser, May E.; Do, Ron; Kenny, Eimear E.; Loos, Ruth J. F.; Terry, James G.; Carr, John Jeffrey; Bis, Joshua C.; Psaty, Bruce M.; Longstreth, W. T.; Young, Kendra A.; Lutz, Sharon M.; Cho, Michael H.; Broome, Jai; Khan, Alyna T.; Wang, Fei Fei; Heard-Costa, Nancy; Seshadri, Sudha; Vasan, Ramachandran S.; Palmer, Nicholette D.; Freedman, Barry I.; Bowden, Donald W.; Yanek, Lisa R.; Kral, Brian G.; Becker, Lewis C.; Peyser, Patricia A.; Bielak, Lawrence F.; Ammous, Farah; Carson, April P.; Hall, Michael E.; Raffield, Laura M.; Rich, Stephen S.; Post, Wendy S.; Tracy, Russel P.; Taylor, Kent D.; Guo, Xiuqing; Mahaney, Michael C.; Curran, Joanne E.; Blangero, John; Clarke, Shoa L.; Haessler, Jeffrey W.; Hu, Yao; Assimes, Themistocles L.; Kooperberg, Charles; Bernhagen, Juergen; Anderson, Christopher D.; Damrauer, Scott M.; Zand, Ramin; Rotter, Jerome I.; de Vries, Paul S.; Dichgans, Martin

John Blangero

个人简介

教育背景

工作经历

荣誉奖项

研究方向