Aoxing Liu

ORCID: 0000-0002-9155-1494
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About
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Research Areas
  • Genetic and phenotypic traits in livestock
  • Reproductive Physiology in Livestock
  • Genetic Mapping and Diversity in Plants and Animals
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Effects of Environmental Stressors on Livestock
  • Genetic Associations and Epidemiology
  • Cancer-related molecular mechanisms research
  • Sexual Differentiation and Disorders
  • Epigenetics and DNA Methylation
  • Immune Cell Function and Interaction
  • Respiratory viral infections research
  • BRCA gene mutations in cancer
  • Sleep and related disorders
  • Acute Myeloid Leukemia Research
  • Cancer Genomics and Diagnostics
  • Machine Learning in Healthcare
  • Birth, Development, and Health
  • Neonatal Respiratory Health Research
  • Viral-associated cancers and disorders
  • Genomics and Rare Diseases
  • Animal Behavior and Welfare Studies
  • Colorectal Cancer Treatments and Studies
  • Stress Responses and Cortisol
  • Frailty in Older Adults
  • Sleep and Wakefulness Research

Institute for Molecular Medicine Finland
2020-2025

University of Helsinki
2021-2025

Broad Institute
2023-2025

Massachusetts General Hospital
2024-2025

Shanghai Institute of Materia Medica
2025

Chinese Academy of Sciences
2025

Nanjing University of Chinese Medicine
2025

Finland University
2023-2024

Ningxia University
2024

University of California, Davis
2024

Mitja Kurki Juha Karjalainen Priit Palta Timo P. Sipilä Kati Kristiansson and 95 more Kati Donner Mary Pat Reeve Hannele Laivuori Mervi Aavikko Mari Kaunisto Anu Loukola Elisa Lahtela Hannele Mattsson Päivi Laiho Pietro Della Briotta Parolo Arto Lehistö Masahiro Kanai Nina Mars Joel Rämö Tuomo Kiiskinen Henrike Heyne Kumar Veerapen Sina Rüeger Susanna Lemmelä Wei Zhou Sanni Ruotsalainen Kalle Pärn Tero Hiekkalinna Sami Koskelainen Teemu Paajanen Vincent Llorens Javier Gracia‐Tabuenca Harri Siirtola Kadri Reis Abdelrahman G. Elnahas Benjamin B. Sun Christopher N. Foley Katriina Aalto‐Setälä Kaur Alasoo Mikko Arvas Kirsi Auro Shameek Biswas Argyro Bizaki-Vallaskangas Olli Carpén Chia‐Yen Chen Oluwaseun Alexander Dada Zhihao Ding Margaret G. Ehm Kari K. Eklund Martti Färkkilâ Hilary K. Finucane Andrea Ganna Awaisa Ghazal Robert Graham Eric M. Green Antti Hakanen Marco Hautalahti Åsa K. Hedman Mikko Hiltunen Reetta Hinttala Iiris Hovatta Xinli Hu Adriana Huertas‐Vázquez Laura Huilaja Julie Hunkapiller Howard Jacob Jan-Nygaard Jensen Heikki Joensuu Sally John Valtteri Julkunen Marc Jung Juhani Junttila Kai Kaarniranta Mika Kähönen Risto Kajanne Lila Kallio Reetta Kälviäinen Jaakko Kaprio Nurlan Kerimov Johannes Kettunen Elina Kilpeläinen Terhi Kilpi K. Klinger Veli‐Matti Kosma Teijo Kuopio Venla Kurra Triin Laisk Jari A. Laukkanen Nathan Lawless Aoxing Liu Simonne Longerich Reedik Mägi Johanna Mäkelä Antti Mäkitie Anders Mälarstig Graham J. Mann Joseph Maranville Athena Matakidou Tuomo J Meretoja Sahar V. Mozaffari

Abstract Population isolates such as those in Finland benefit genetic research because deleterious alleles are often concentrated on a small number of low-frequency variants (0.1% ≤ minor allele frequency < 5%). These survived the founding bottleneck rather than being distributed over large ultrarare variants. Although this effect is well established Mendelian genetics, its value common disease genetics less explored 1,2 . FinnGen aims to study genome and national health register data...

10.1038/s41586-022-05473-8 article EN cc-by Nature 2023-01-18
Mitja Kurki Juha Karjalainen Priit Palta Timo P. Sipilä Kati Kristiansson and 95 more Kati Donner Mary Pat Reeve Hannele Laivuori Mervi Aavikko Mari Kaunisto Anu Loukola Elisa Lahtela Hannele Mattsson Päivi Laiho Pietro Della Briotta Parolo Arto Lehistö Masahiro Kanai Nina Mars Joel Rämö Tuomo Kiiskinen Henrike Heyne Kumar Veerapen Sina Rüeger Susanna Lemmelä Wei Zhou Sanni Ruotsalainen Kalle Pärn Tero Hiekkalinna Sami Koskelainen Teemu Paajanen Vincent Llorens Javier Gracia‐Tabuenca Harri Siirtola Kadri Reis Abdelrahman G. Elnahas Katriina Aalto‐Setälä Kaur Alasoo Mikko Arvas Kirsi Auro Shameek Biswas Argyro Bizaki-Vallaskangas Olli Carpén Chia‐Yen Chen Oluwaseun Alexander Dada Zhihao Ding Margaret G. Ehm Kari K. Eklund Martti Färkkilâ Hilary K. Finucane Andrea Ganna Awaisa Ghazal Robert Graham Eric Green Antti Hakanen Marco Hautalahti Åsa K. Hedman Mikko Hiltunen Reetta Hinttala Iiris Hovatta Xinli Hu Adriana Huertas‐Vázquez Laura Huilaja Julie Hunkapiller Howard J. Jacob Jan-Nygaard Jensen Heikki Joensuu Sally John Valtteri Julkunen Marc Jung Juhani Junttila Kai Kaarniranta Mika Kähönen Risto Kajanne Lila Kallio Reetta Kälviäinen Jaakko Kaprio Nurlan Kerimov Johannes Kettunen Elina Kilpeläinen Terhi Kilpi K. Klinger Veli‐Matti Kosma Teijo Kuopio Venla Kurra Triin Laisk Jari A. Laukkanen Nathan Lawless Aoxing Liu Simonne Longerich Reedik Mägi Johanna Mäkelä Antti Mäkitie Anders Mälarstig Arto Mannermaa Joseph Maranville Athena Matakidou Tuomo J Meretoja Sahar V. Mozaffari Mari Niemi Marianna Niemi

ABSTRACT Population isolates such as Finland provide benefits in genetic studies because the allelic spectrum of damaging alleles any gene is often concentrated on a small number low-frequency variants (0.1% ≤ minor allele frequency < 5%), which survived founding bottleneck, opposed to being distributed over much larger ultra--rare variants. While this advantage well-- established Mendelian genetics, its value common disease genetics has been less explored. FinnGen aims study genome and...

10.1101/2022.03.03.22271360 preprint EN cc-by medRxiv (Cold Spring Harbor Laboratory) 2022-03-06
Seyedeh M. Zekavat Shu‐Hong Lin Alexander G. Bick Aoxing Liu Kaavya Paruchuri and 95 more Chen Wang Md Mesbah Uddin Yixuan Ye Zhaolong Yu Xiaoxi Liu Yoichiro Kamatani Romit Bhattacharya James P. Pirruccello Akhil Pampana Po−Ru Loh Puja Kohli Steven A. McCarroll Krzysztof Kiryluk Benjamin M. Neale Iuliana Ionita‐Laza Eric A. Engels Derek W. Brown Jordan W. Smoller Robert C. Green Elizabeth W. Karlson Matthew S. Lebo Patrick T. Ellinor Scott T. Weiss Mark J. Daly Satoshi Koyama Kaoru Ito Yukihide Momozawa Koichi Matsuda Yuji Yamanashi Yoichi Furukawa Takayuki Morisaki Yoshinori Murakami Kaori Muto Akiko Nagai Wataru Obara Ken Yamaji Kazuhisa Takahashi Satoshi Asai Yasuo Takahashi Takao Suzuki Nobuaki Sinozaki Hiroki Yamaguchi Shiro Minami Shigeo Murayama Kozo Yoshimori Satoshi Nagayama Daisuke Obata Masahiko Higashiyama Akihide Masumoto Yukihiro Koretsune Aarno Palotie Adam Ziemann Adele A. Mitchell Adriana Huertas‐Vázquez Aino Salminen Airi Jussila Aki S. Havulinna Alex Mackay Ali Abbasi Amanda Elliott Amy L. Cole Anastasia Shcherban Anders Mälarstig Andrea Ganna Andrey Loboda Anna Podgornaia Anne Lehtonen Anne Pitkäranta Anne M. Remes Annika Auranen Antti Hakanen Antti Palomäki Anu Jalanko Anu Loukola Aparna Chhibber Apinya Lertratanakul Arto Lehistö Graham J. Mann Åsa K. Hedman Audrey Y. Chu Aviv Madar Awaisa Ghazal Benjamin Challis Benjamin B. Sun Beryl B. Cummings Bridget Riley‐Gillis Caroline S. Fox Chia‐Yen Chen Clarence Wang Clément Chatelain Daniel Gordin Danjuma Quarless Danny Oh David F. Choy David A. Close

10.1038/s41591-021-01371-0 article EN Nature Medicine 2021-06-01

Novel immunisation methods against respiratory syncytial virus (RSV) are emerging, but knowledge of risk factors for severe RSV disease is insufficient optimal targeting interventions them. Our aims were to identify predictors hospital admission from registry-based data and develop validate a clinical prediction model guide immunoprophylaxis infants younger than 1 year.In this development validation study, we studied all born in Finland between June 1, 1997, May 31, 2020, Sweden 2006, along...

10.1016/s2589-7500(23)00175-9 article EN cc-by-nc-nd The Lancet Digital Health 2023-10-25

Studies show that sex plays a role in stress-related depression, with women experiencing higher vulnerability to its effect. Two major targets of antidepressants are brain-derived neurotrophic factor (BDNF) and cyclic adenosine monophosphate response element–binding protein (CREB). The aim this study was investigate the levels CREB, phosphorylation CREB (pCREB), BDNF brain regions male female rats after stress recovery. pCREB were examined CA1, CA2, CA3, paraventricular nucleus thalamus...

10.1093/cercor/bhn225 article EN cc-by-nc Cerebral Cortex 2008-12-10

Genotype-by-environment (G × E) interactions could play an important role in cattle populations, and it should be considered breeding programmes to select the best sires for different environments. The objectives of this study were G E female fertility traits Danish Holstein dairy population using a reaction norm model (RNM), detect particular genomic regions contributing performance these interactions. In total 4534 bulls genotyped by Illumina BovineSNP50 BeadChip. An RNM with...

10.1038/s41437-019-0192-4 article EN cc-by Heredity 2019-02-13

The availability of whole genome sequencing (WGS) data enables the discovery causative single nucleotide polymorphisms (SNPs) or SNPs in high linkage disequilibrium with SNPs. This study investigated effects integrating selected from imputed WGS into 54K chip on genomic prediction Danish Jersey. SNPs, mainly including peaks quantitative trait loci, structure variants, regulatory regions genes, and within genes strong predicted variant effect predictor, were previous analyses for dairy breeds...

10.1038/s41437-019-0246-7 article EN cc-by Heredity 2019-07-05

Abstract The percentage of people without children over their lifetime is approximately 25% in men and 20% women. Individual diseases have been linked to childlessness, mostly women, yet we lack a comprehensive picture the effect early-life on childlessness. We examined all individuals born 1956–1968 (men) 1956–1973 (women) Finland ( n = 1,035,928) Sweden 1,509,092) completion reproductive lifespan 2018. Leveraging nationwide registers, associated sociodemographic information with 414 across...

10.1038/s41562-023-01763-x article EN cc-by Nature Human Behaviour 2023-12-18

ABSTRACT Sex chromosome trisomies (SCT) are the most common whole aneuploidy in humans. Yet, our understanding of prevalence and associated health outcomes is largely driven by observational studies clinically diagnosed cases, resulting a disproportionate focus on 47,XXY hypogonadism. We analyzed microarray intensity data sex chromosomes for 1.5 million individuals enrolled three large cohorts—Million Veteran Program, FinnGen, UK Biobank—to identify with 47,XXY, 47,XYY, 47,XXX. examined...

10.1101/2025.01.31.25321488 preprint EN cc-by medRxiv (Cold Spring Harbor Laboratory) 2025-02-02

Vaccine immunogenicity is influenced by the vaccinee's genetic background. Here, we perform a genome-wide association study of vaccine-induced SARS-CoV-2-specific immunoglobulin G (IgG) antibody titers and T cell immune responses in 1,559 mRNA-1273 537 BNT162b2 vaccinees Japanese ancestry. are associated with heavy chain (IGH) major histocompatibility complex (MHC) locus, MHC. The lead variants at IGH contain population-specific missense variant (rs1043109-C; p.Leu192Val) constant gamma 1...

10.1016/j.xgen.2025.100783 article EN cc-by-nc-nd Cell Genomics 2025-03-01

Due to the complexity of longevity trait in dairy cattle, two groups definitions are widely used measure longevity, either covering full lifespan or representing only a part it achieve an early selection. Usually, one group definition is breeding program for population, and genetic studies on comparisons scarce. Based data eight traits well both definitions, current study investigated parameters architectures Holsteins. Heritabilities correlations were estimated using single-trait...

10.3389/fgene.2021.634986 article EN cc-by Frontiers in Genetics 2021-02-25

Heat stress is a major cause of welfare issues and economic losses to the worldwide dairy cattle industry. Genetic selection for heat tolerance has great potential positively affect industry, as gains are permanent cumulative over generations. Rectal temperature (RT) hypothesized be good indicator trait tolerance. Therefore, this study investigated genetic architecture RT by estimating parameters, performing genome-wide association studies, biologically validating candidate genes identified...

10.3168/jds.2020-18725 article EN cc-by-nc-nd Journal of Dairy Science 2021-02-15

Women show a higher prevalence for depression than men. However, the biological basis of gender differences in stress response and recovery still remain poorly understood. Therefore, aim study was to assess acute stress, chronic rats. Our results showed that decreased male body weight but had no effect on female Open field test demonstrated behavioral changes grooming velocity after recovery. Increased activity hypothalamic-pituitary-adrenocortical axis reflected by adrenal hypertrophy...

10.1093/cercor/bhn035 article EN Cerebral Cortex 2008-03-20

The objective of the present study was to estimate (co)variance components female fertility traits in Chinese Holsteins, considering different parities as traits. Data on 88,647 females with 215,632 records (parities) were collected during 2000 2014 from 32 herds Sanyuan Lvhe Dairy Cattle Center, Beijing, China. analyzed included interval calving first insemination, last days open, conception rate at number inseminations per and non-return rates within 56 after insemination.The descriptive...

10.1186/s40104-017-0189-x article EN cc-by Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology 2017-06-29

Abstract Background The effect of heat stress on livestock production is a worldwide issue. Animal performance influenced by exposure to harsh environmental conditions potentially causing genotype-by-environment interactions (G × E), especially in highproducing animals. In this context, the main objectives study were (1) detect time periods which heifer fertility traits are more sensitive high temperature and/or humidity, (2) investigate G E due traits, and, (3) identify genomic regions...

10.1186/s12864-021-07496-3 article EN cc-by BMC Genomics 2021-03-17
Essi Viippola Sara Kuitunen Rodosthenis S. Rodosthenous Andrius Vabalas Tuomo Hartonen and 95 more Pekka Vartiainen Joanne Demmler Anna‐Leena Vuorinen Aoxing Liu Aki S. Havulinna Vincent Llorens Kira E Detrois Feiyi Wang Matteo Ferro Antti Karvanen J German Sakari Jukarainen Javier Gracia‐Tabuenca Tero Hiekkalinna Sami Koskelainen Tuomo Kiiskinen Elisa Lahtela Susanna Lemmelä Teemu Paajanen Harri Siirtola Mary Pat Reeve Kati Kristiansson Minna Brunfeldt Mervi Aavikko Finn Gen Markus Perola Andrea Ganna Aarno Palotie Mark J. Daly Bridget Riley-Gills Howard Jacob Dirk S. Paul Athena Matakidou Adam Platt Heiko Runz Sally John George Okafo Nathan Lawless Heli Salminen‐Mankonen Robert M. Plenge Joseph Maranville Mark I. McCarthy Margaret G. Ehm Kirsi Auro Simonne Longerich Caroline S. Fox Anders Mälarstig K. Klinger Clément Chatelain Matthias Gossel Karol Estrada Robert Graham Robert Yang Chris O’Donnell Tomi P. Mäkelä Jaakko Kaprio Petri Virolainen Antti Hakanen Terhi Kilpi Jukka Partanen Anne Pitkäranta Taneli Raivio Raisa Serpi Tarja Laitinen Veli‐Matti Kosma Jari A. Laukkanen Marco Hautalahti Outi Tuovila Raimo Pakkanen Jeffrey F. Waring Bridget Riley‐Gillis Fedik Rahimov Ioanna Tachmazidou Chia‐Yen Chen Heiko Runz Zhihao Ding Marc Jung Shameek Biswas Rion Pendergrass Margaret G. Ehm David Pulford Neha Raghavan Adriana Huertas‐Vázquez Jae-Hoon Sul Anders Mälarstig Xinli Hu Åsa K. Hedman K. Klinger Robert Graham Manuel A. Rivas Dawn Waterworth Nicole Renaud Ma’en Obeidat Samuli Ripatti Johanna Schleutker

10.1093/ije/dyad091 article EN cc-by International Journal of Epidemiology 2023-06-26

Importance The reported phenotypes of men with 47,XXY and 47,XYY syndromes include tall stature, multisystem comorbidities, poor health-related quality life (HRQOL). However, knowledge about these sex chromosome aneuploidy (SCA) conditions has been derived from studies in the less than 15% patients who are clinically diagnosed also lack diversity age genetic ancestry. Objectives To determine prevalence undiagnosed X or Y among enrolled Million Veteran Program (MVP); to describe military...

10.1001/jamanetworkopen.2024.4113 article EN cc-by-nc-nd JAMA Network Open 2024-03-29

Abstract Short-term mortality risk, which is indicative of individual frailty, serves as a marker for aging. Previous age clocks focused on predicting either chronological or longer-term mortality. Aging short-term are lacking and their algorithmic fairness remains unexamined. We developed deep learning model to predict 1-year using nationwide longitudinal data from the Finnish population (FinRegistry; n = 5.4 million), incorporating more than 8,000 features spanning up 50 years. achieved an...

10.1038/s43587-024-00657-5 article EN cc-by Nature Aging 2024-06-24

High mortality and involuntary culling rates cause great economic losses to the worldwide dairy cattle industry. However, there is low emphasis on wellness traits in replacement animals (dairy calves heifers) during their development stages modern breeding programs. Therefore, main objectives of this study were estimate genetic parameters (replacement traits) obtain correlations with 12 cow health longevity Chinese Holstein population. Seven analyzed, including birth weight, survival from 3...

10.3168/jds.2021-21450 article EN cc-by Journal of Dairy Science 2022-07-13
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