Author details

Full Name

Momoko Horikoshi

Affiliation

ORCID

Career Start Year

2005

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37503126	Understanding the genetic complexity of puberty timing across the allele frequency spectrum.	medRxiv	2023
37903429	Natural Selection Signatures in the Hondo and Ryukyu Japanese Subpopulations.		2023
37612283	Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects.	Nat Commun	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
33402679	Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
34226521	Structural basis of ethnic-specific variants of PAX4 associated with type 2 diabetes.	Hum Genome Var	2021
33607655	Genome-wide association studies identify two novel loci conferring susceptibility to diabetic retinopathy in Japanese patients with type 2 diabetes.	Hum Mol Genet	2021
33558525	Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
32514122	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Nat Genet	2020
32152314	Author Correction: Characterizing rare and low-frequency height-associated variants in the Japanese population.	Nat Commun	2020
33045005	Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.	PLoS Genet	2020
33020668	Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.	Nature Genetics	2020
30830152	Association Between Genetic Risk and Development of Type 2 Diabetes in a General Japanese Population: The Hisayama Study.	Journal of Clinical Endocrinology and Metabolism	2019
31562340	Characterizing rare and low-frequency height-associated variants in the Japanese population.	Nat Commun	2019
30718926	Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population.	Nat Genet	2019
29773799	Elucidating the genetic architecture of reproductive ageing in the Japanese population.	Nat Commun	2018
30087441	Author Correction: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition.	Nat Genet	2018
29309628	Genome-wide association study of offspring birth weight in 86â¿¿577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics.	Hum Mol Genet	2018
29703846	LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.	Circulation	2018
29632379	Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition.	Nat Genet	2018
29360107	Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2018
28293907	How Can Genetic Studies Help Us to Understand Links Between Birth Weight and Type 2 Diabetes?	Current Diabetes Reports	2017
28911207	Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution.	Hum Mol Genet	2017
28443625	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	Nat Commun	2017
29257133	Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2017
27680694	Genome-wide associations for birth weight and correlations with adult disease.	Nature	2016
26978208	Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight.	JAMA	2016
27225129	Genome-wide association study identifies 74 loci associated with educational attainment.	Nature	2016
26911676	Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.	Hum Mol Genet	2016
27398621	The genetic architecture of type 2 diabetes.	Nature	2016
26604143	Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.	Hum Mol Genet	2016
26635082	Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation.	Nat Commun	2015
25281659	A novel common variant in DCST2 is associated with length in early life and height in adulthood.	Hum Mol Genet	2015
25961943	The impact of low-frequency and rare variants on lipid levels.	Nat Genet	2015
26482879	Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis.	Nat Genet	2015
26132169	Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation.	PLoS Genet	2015
24509480	Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.	Nat Genet	2014
23945395	Genome-wide association study identifies three novel loci for type 2 diabetes.	Hum Mol Genet	2014
23704328	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.	Hum Mol Genet	2013
23824655	The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis.	PLoS Med	2013
23202124	New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.	Nat Genet	2013
22983607	Depletion of homeodomain-interacting protein kinase 3 impairs insulin secretion and glucose tolerance in mice.	Diabetologia	2012
22971728	Associations of variations in the MRF2/ARID5B gene with susceptibility to type 2 diabetes in the Japanese population.	Journal of Human Genetics	2012
22885924	Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.	Nat Genet	2012
22843499	Genome-wide meta-analysis of common variant differences between men and women.	Hum Mol Genet	2012
22499789	Expression-based genome-wide association study links the receptor CD44 in adipose tissue with type 2 diabetes.	Proc Natl Acad Sci U S A	2012
22456796	A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations.	Hum Mol Genet	2012
22992776	Variations with modest effects have an important role in the genetic background of type 2 diabetes and diabetes-related traits.	Journal of Human Genetics	2012
21873549	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.	Diabetes	2011