Tenghao Zheng

ORCID: 0000-0003-1587-7481
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Research Areas
  • Gastrointestinal motility and disorders
  • Diet and metabolism studies
  • Gut microbiota and health
  • Helicobacter pylori-related gastroenterology studies
  • Digestive system and related health
  • Nutritional Studies and Diet
  • Congenital gastrointestinal and neural anomalies
  • COVID-19 Clinical Research Studies
  • Liver Disease Diagnosis and Treatment
  • Dietary Effects on Health
  • SARS-CoV-2 and COVID-19 Research
  • Anorectal Disease Treatments and Outcomes
  • Pelvic floor disorders treatments
  • Ion channel regulation and function
  • Clostridium difficile and Clostridium perfringens research
  • RNA modifications and cancer
  • Microscopic Colitis
  • Celiac Disease Research and Management
  • Ion Channels and Receptors
  • Gastroesophageal reflux and treatments
  • Infant Health and Development
  • Blood groups and transfusion
  • Tryptophan and brain disorders
  • Barrier Structure and Function Studies
  • Ion Transport and Channel Regulation

Monash University
2020-2025

Karolinska Institutet
2016-2023

Norwegian Institute of Public Health
2021

Biogipuzkoa Health Research Institute
2020

Zhengzhou University
2010-2014

Henan Provincial People's Hospital
2014

David Ellinghaus Frauke Degenhardt Luís Bujanda Marı́a Buti Agustı́n Albillos and 95 more Pietro Invernizzi Javier Fernández Daniele Prati Guido Baselli Rosanna Asselta Marit M. Grimsrud Chiara Milani Fátima Aziz Jan Christian Kässens Sandra May Mareike Wendorff Lars Wienbrandt Florian Uellendahl-Werth Tenghao Zheng Xiaoli Yi Raúl de Pablo Adolfo Garrido Chercoles Adriana Palom Alba-Estela Garcia-Fernandez Francisco Rodríguez‐Frías Alberto Zanella Alessandra Bandera Alessandro Protti Alessio Aghemo Ana Lleò Andrea Biondi Andrea Caballero-Garralda Andrea Gori Anja Tanck Anna Carreras Anna Latiano Anna Ludovica Fracanzani Anna Peschuck Antonio Julià Antonio Artigas Antonio Voza David Jiménez Beatriz Muñoz Beatriz Nafría Jiménez Carmen Quereda Cinzia Paccapelo Christoph Gassner Claudio Angelini Cristina Cea Aurora Solier David Pestaña Eduardo Muñiz‐Díaz Elena Sandoval Elvezia Maria Paraboschi Enrique Navas F. García‐Sánchez Ferruccio Ceriotti Filippo Martinelli Boneschi Flora Peyvandi Francesco Blasi Luís Téllez Albert Blanco‐Grau Georg Hemmrich‐Stanisak Giacomo Grasselli Giorgio Costantino Giulia Cardamone Giuseppe Foti Serena Aneli Hayato Kurihara Hesham ElAbd Ilaria My Iván Galván‐Femenía Javier Martı́n Jeanette Erdmann José Ferrusquía‐Acosta Koldo García‐Etxebarria Laura Izquierdo‐Sánchez Laura Rachele Bettini Lauro Sumoy Leonardo Terranova Leticia Moreira Luigi Santoro Luigia Scudeller Francisco Mesonero Luisa Roade Malte Rühlemann Marco Schaefer Maria Carrabba Mar Riveiro‐Barciela Maria E. Figuera Basso Maria Grazia Valsecchi Maria De Santis Marialbert Acosta‐Herrera Mariella D’Angiò Marina Baldini Marina Elena Cazzaniga Martin Schulzky Maurizio Cecconi Michael Wittig Michele Ciccarelli

There is considerable variation in disease behavior among patients infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes 2019 (Covid-19). Genomewide association analysis may allow for identification of potential genetic factors involved development Covid-19.

10.1056/nejmoa2020283 article EN New England Journal of Medicine 2020-06-17
Chris Eijsbouts Tenghao Zheng Nicholas A. Kennedy Ferdinando Bonfiglio Carl A. Anderson and 95 more Loukas Moutsianas Jo Holliday Jingchunzi Shi Suyash Shringarpure Michelle Agee Stella Aslibekyan Adam Auton Robert K. Bell Katarzyna Bryc Sarah Clark Sarah L. Elson Kipper Fletez‐Brant Pierre Fontanillas Nicholas A. Furlotte Pooja Gandhi Karl Heilbron Barry Hicks David A. Hinds Karen E. Huber Ethan M. Jewett Yunxuan Jiang Aaron Kleinman Keng‐Han Lin Nadia K. Litterman Marie K. Luff Jey C. McCreight Matthew H. McIntyre Kimberly F. McManus Joanna L. Mountain Sahar V. Mozaffari Priyanka Nandakumar Elizabeth S. Noblin Carrie A. M. Northover Jared O’Connell Aaron A. Petrakovitz Steven J. Pitts G. David Poznik J. Fah Sathirapongsasuti Anjali J. Shastri Janie F. Shelton Chao Tian Joyce Y. Tung Robert J. Tunney Vladimir Vacic Xin Wang Amir S. Zare Alexandru-Ioan Voda Purna Kashyap Lin Chang Emeran A. Mayer Margaret Heitkemper Gregory S. Sayuk Tamar Ringel‐Kulka Yehuda Ringel William D. Chey Shanti Eswaran Juanita L. Merchant Robert J. Shulman Luís Bujanda Koldo García‐Etxebarria Aldona Dlugosz Greger Lindberg Peter T. Schmidt Pontus Karling Bodil Ohlsson Susanna Walter Åshild Faresjö Magnus Simrén Jonas Halfvarson Piero Portincasa Giovanni Barbara Paolo Usai–Satta Matteo Neri Gerardo Nardone Rosario Cuomo Francesca Galeazzi Massimo Bellini Anna Latiano Lesley A. Houghton Daisy Jonkers Alexander Kurilshikov Rinse K. Weersma Mihai G. Netea Jonas Tesarz Annika Gauss Miriam Goebel‐Stengel Viola Andresen Thomas Frieling Christian Pehl Rainer Schaefert Beate Niesler Wolfgang Lieb Kurt Hanevik Nina Langeland Knut‐Arne Wensaas

Abstract Irritable bowel syndrome (IBS) results from disordered brain–gut interactions. Identifying susceptibility genes could highlight the underlying pathophysiological mechanisms. We designed a digestive health questionnaire for UK Biobank and combined identified cases with IBS independent cohorts. conducted genome-wide association study 53,400 433,201 controls replicated significant associations in 23andMe panel (205,252 1,384,055 controls). Our confirmed six genetic loci IBS. Implicated...

10.1038/s41588-021-00950-8 article EN cc-by Nature Genetics 2021-11-01

BACKGROUND: Fermentation of dietary fiber by the gut microbiota leads to production metabolites called short-chain fatty acids, which lower blood pressure and exert cardioprotective effects. Short-chain acids activate host signaling responses via functionally redundant receptors GPR41 GPR43, are highly expressed immune cells. Whether how these protect against hypertension or mediate effects remains unknown. METHODS: Cardiovascular phenotype was assessed in untreated Ang II (angiotensin II)...

10.1161/circresaha.124.325770 article EN Circulation Research 2025-01-22

IBS is a common gut disorder of uncertain pathogenesis. Among other factors, genetics and certain foods are proposed to contribute. Congenital sucrase-isomaltase deficiency (CSID) rare genetic form disaccharide malabsorption characterised by diarrhoea, abdominal pain bloating, which features IBS. We tested (SI) gene variants for their potential relevance in IBS.We sequenced SI exons seven familial cases, screened four CSID mutations (p.Val557Gly, p.Gly1073Asp, p.Arg1124Ter p.Phe1745Cys)...

10.1136/gutjnl-2016-312456 article EN cc-by-nc Gut 2016-11-21

Abstract Aims Animal models are regularly used to test the role of gut microbiome in hypertension. Small-scale pre-clinical studies have investigated changes angiotensin II hypertensive model. However, is influenced by internal and external experimental factors, which not considered study design. Once these factors accounted for, it unclear if signatures reproduceable. We aimed determine influence treatment on using a large diverse cohort mice quantify magnitude other contribute variations....

10.1093/cvr/cvae062 article EN cc-by Cardiovascular Research 2024-03-22

Patients with irritable bowel syndrome (IBS) often associate their symptoms to certain foods. In congenital sucrase-isomaltase deficiency (CSID), recessive mutations in the SI gene (coding for disaccharidase digesting sucrose and 60% of dietary starch)1 cause clinical features IBS through colonic accumulation undigested carbohydrates, triggering symptoms.2 Hence, a previous study,3 we hypothesized that CSID variants reducing enzymatic activity may contribute development symptoms. We detected...

10.1016/j.cgh.2018.01.047 article EN cc-by-nc-nd Clinical Gastroenterology and Hepatology 2018-02-21
David Ellinghaus Frauke Degenhardt Luís Bujanda Marı́a Buti Agustı́n Albillos and 95 more Pietro Invernizzi Javier Fernández Daniele Prati Guido Baselli Rosanna Asselta Marit M. Grimsrud Chiara Milani Fátima Aziz Jan Christian Kässens Sandra May Mareike Wendorff Lars Wienbrandt Florian Uellendahl-Werth Tenghao Zheng Xiaoli Yi Raúl de Pablo Adolfo Garrido Chercoles Adriana Palom Alba-Estela Garcia-Fernandez Francisco Rodríguez‐Frías Alberto Zanella Alessandra Bandera Alessandro Protti Alessio Aghemo Ana Lleò Andrea Biondi Andrea Caballero-Garralda Andrea Gori Anja Tanck Anna Latiano Anna Ludovica Fracanzani Anna Peschuk Antonio Julià Antonio Artigas Antonio Voza David González Jiménez Beatriz Muñoz Beatriz Nafría Jiménez Carmen Quereda Claudio Angelini Cristina Cea Aurora Solier David Pestaña Elena Sandoval Elvezia Maria Paraboschi Enrique Navas Ferruccio Ceriotti Filippo Martinelli Boneschi Flora Peyvandi Francesco Blasi Luís Téllez Albert Blanco‐Grau Giacomo Grasselli Giorgio Costantino Giulia Cardamone Giuseppe Foti Serena Aneli Hayato Kurihara Hesham ElAbd Ilaria My Javier Martı́n Jeanette Erdmann José Ferrusquía‐Acosta Koldo García‐Etxebarria Laura Izquierdo‐Sánchez Laura Rachele Bettini Leonardo Terranova Leticia Moreira Luigi Santoro Luigia Scudeller Francisco Mesonero Luisa Roade Marco Schaefer Maria Carrabba Maria del Mar Riveiro Barciela Maria E. Figuera Basso Maria Grazia Valsecchi Maria De Santis Marialbert Acosta‐Herrera Mariella D’Angiò Marina Baldini Marina Elena Cazzaniga Martin Schulzky Maurizio Cecconi Michael Wittig Michele Ciccarelli Miguel Ángel Rodríguez Gandía M. Bocciolone Monica Miozzo Nicole Braun Nilda Martínez Orazio Palmieri Paola Faverio Paoletta Preatoni Paolo Bonfanti

ABSTRACT Background Respiratory failure is a key feature of severe Covid-19 and critical driver mortality, but for reasons poorly defined affects less than 10% SARS-CoV-2 infected patients. Methods We included 1,980 patients with respiratory at seven centers in the Italian Spanish epicenters pandemic Europe (Milan, Monza, Madrid, San Sebastian Barcelona) genome-wide association analysis. After quality control exclusion population outliers, 835 1,255 population-derived controls from Italy,...

10.1101/2020.05.31.20114991 preprint EN medRxiv (Cold Spring Harbor Laboratory) 2020-06-02

Objective Haemorrhoidal disease (HEM) affects a large and silently suffering fraction of the population but its aetiology, including suspected genetic predisposition, is poorly understood. We report first genome-wide association study (GWAS) meta-analysis to identify risk factors for HEM date. Design conducted GWAS 218 920 patients with 725 213 controls European ancestry. Using summary statistics, we performed multiple correlation analyses between other traits as well calculated polygenic...

10.1136/gutjnl-2020-323868 article EN cc-by Gut 2021-04-22

Traditional cardiovascular risk factors, including hypertension, only explain part of major adverse cardiac events (MACEs). Understanding what other factors contribute to MACE is essential for prevention. Constipation shares common with hypertension and associated an increased several diseases. We hypothesized that constipation underappreciated factor MACE. used the population healthcare genomic data in UK Biobank (

10.1152/ajpheart.00519.2024 article EN AJP Heart and Circulatory Physiology 2024-08-16

Gut dysmotility is associated with constipation, diarrhea, and functional gastrointestinal disorders like irritable bowel syndrome (IBS), although its molecular underpinnings are poorly characterized. We studied stool frequency (defined by the number of movements per day, based on questionnaire data) as a proxy for gut motility in GWAS meta-analysis including 167,875 individuals from UK Biobank four smaller population-based cohorts. identify 14 loci (p ≤ 5.0 × 10−8). Gene set pathway...

10.1016/j.xgen.2021.100069 article EN cc-by-nc-nd Cell Genomics 2021-12-01

Membrane contact sites between organelles are critical for the transfer of biomolecules. Lipid droplets store fatty acids and form contacts with mitochondria, which regulate acid oxidation adenosine triphosphate production. Protein compartmentalization at lipid droplet-mitochondria their effects on biological processes poorly described. Using proximity-dependent biotinylation methods, we identify 71 proteins sites, including a multimeric complex containing extended synaptotagmin (ESYT) 1,...

10.1038/s41467-025-57405-5 article EN cc-by-nc-nd Nature Communications 2025-03-03

This study aimed to investigate the presence of plasma minichromosome maintenance complex component 6 (MCM6) mRNA and protein levels in hepatocellular carcinoma (HCC) patients evaluate their diagnostic value for HCC.Blood samples were collected from 61 HCC 29 cirrhotic patients, 30 healthy individuals. Circulating RNA was extracted all samples. The MCM6 amplified quantified by real-time polymerase chain reaction. Plasma α-fetoprotein (AFP) measured enzyme-linked immunosorbent assay.In...

10.1111/hepr.12303 article EN Hepatology Research 2014-01-23

Abstract Fermentation of dietary fibre by the gut microbiota leads to production metabolites called short-chain fatty acids (SCFAs), which have emerged as potent regulators immune, metabolic, and tissue barrier functions. More recently, a high diet SCFA supplementation were shown lower blood pressure be cardio-protective. SCFAs activate host signalling responses via receptors GPR41 GPR43, redundancy in their pathways. Whether these play role hypertension or mediate cardio-protective effects...

10.1101/2023.03.20.533376 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2023-03-22

The Ca2+-activated Cl- channel, anoctamin 1 (Ano1, also known as transmembrane protein 16A) contributes to intestinal pacemaking, fluid secretion, cellular excitability, and tissue development. human ANO1 promoter contains binding sites for the glioma-associated oncogene (Gli) proteins. We investigated regulation of transcription by Gli. activity was determined using a luciferase reporter system. Binding functional effects Glis on expression were demonstrated chromatin immunoprecipitation,...

10.1096/fj.201802373r article EN The FASEB Journal 2019-02-25
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