Manabu Funayama

Manabu Funayama

Juntendo University

H-index: 39

Asia-Japan

About Manabu Funayama

Manabu Funayama, With an exceptional h-index of 39 and a recent h-index of 29 (since 2020), a distinguished researcher at Juntendo University,

His recent articles reflect a diverse array of research interests and contributions to the field:

Generation of a control iPS cell line (JUCGRMi005-A) with no abnormalities in Parkinson's disease-related genes

Generation of a control iPS cell line (JUCGRMi006-A) with no abnormalities in Parkinson's disease-related genes

Pathogenesis of Parkinson’s disease: from hints from monogenic familial PD to biomarkers

Investigation of 22q11. 2 Deletion in Japanese Early-Onset Parkinsonism

Analysis of LIN28A variants in patients with Parkinson’s disease

Molecular genetics of Parkinson’s disease: Contributions and global trends

Embracing monogenic Parkinson's disease: the MJFF Global Genetic PD cohort

Long‐Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease

Manabu Funayama Information

University

Position

Research Institute of Disease of Old Age Graduate School of Medicine

Citations(all)

6746

Citations(since 2020)

3129

Cited By

4708

hIndex(all)

39

hIndex(since 2020)

29

i10Index(all)

78

i10Index(since 2020)

63

Email

University Profile Page

Juntendo University

Google Scholar

View Google Scholar Profile

Top articles of Manabu Funayama

Title

Journal

Author(s)

Publication Date

Generation of a control iPS cell line (JUCGRMi005-A) with no abnormalities in Parkinson's disease-related genes

Stem Cell Research

Kei-ichi Ishikawa

Takahiro Shiga

Manabu Funayama

Nobutaka Hattori

Wado Akamatsu

2024/2/1

Generation of a control iPS cell line (JUCGRMi006-A) with no abnormalities in Parkinson's disease-related genes

Stem Cell Research

Kei-ichi Ishikawa

Takahiro Shiga

Manabu Funayama

Nobutaka Hattori

Wado Akamatsu

2024/2/1

Pathogenesis of Parkinson’s disease: from hints from monogenic familial PD to biomarkers

Journal of Neural Transmission

Nobutaka Hattori

Manabu Funayama

Yuzuru Imai

Taku Hatano

2024/3/13

Investigation of 22q11. 2 Deletion in Japanese Early-Onset Parkinsonism

Movement disorders: official journal of the Movement Disorder Society

Stephanie Ong

Manabu Funayama

Yuki Mangyoku

Hiromichi Kawai

Hiroyo Yoshino

...

2024/3

Analysis of LIN28A variants in patients with Parkinson’s disease

Journal of Human Genetics

Hao Peng

Yuanzhe Li

Hiroyo Yoshino

Mai Shimizu

Kenya Nishioka

...

2023/5

Molecular genetics of Parkinson’s disease: Contributions and global trends

Manabu Funayama

Kenya Nishioka

Yuanzhe Li

Nobutaka Hattori

2023/3

Embracing monogenic Parkinson's disease: the MJFF Global Genetic PD cohort

Movement Disorders

Eva‐Juliane Vollstedt

Susen Schaake

Katja Lohmann

Shalini Padmanabhan

Alexis Brice

...

2023/2

Long‐Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease

Movement Disorders

Kensuke Daida

Manabu Funayama

Kimberley J Billingsley

Laksh Malik

Abigail Miano‐Burkhardt

...

2023/12

Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study

The Lancet Neurology

Mie Rizig

Sara Bandres-Ciga

Mary B Makarious

Oluwadamilola Omolara Ojo

Peter Wild Crea

...

2023/11/1

Propagative α-synuclein seeds as serum biomarkers for synucleinopathies

Nature medicine

Ayami Okuzumi

Taku Hatano

Gen Matsumoto

Shuko Nojiri

Shin-ichi Ueno

...

2023/6

Clinical manifestations and molecular backgrounds of Parkinson's disease regarding genes identified from familial and population studies

Kenya Nishioka

Yuzuru Imai

Hiroyo Yoshino

Yuanzhe Li

Manabu Funayama

...

2022/6/2

Genotype-phenotype correlation of Parkinson's disease with PRKN variants

Neurobiology of Aging

Hiroyo Yoshino

Yuanzhe Li

Kenya Nishioka

Kensuke Daida

Arisa Hayashida

...

2022/6/1

Deep brain stimulation for a patient with familial Parkinson's disease harboring CHCHD2 p. T61I

Movement Disorders Clinical Practice

Hikaru Kamo

Genko Oyama

Kenya Nishioka

Manabu Funayama

Nobutaka Hattori

2022/4

A complex form of hereditary spastic paraplegia harboring a novel variant, p. W1515*, in the SPG11 gene

Eneurologicalsci

Kensuke Daida

Yosuke Nishioka

Yuanzhe Li

Hiroyo Yoshino

Manabu Funayama

...

2022/3/1

α‐Synuclein V15A variant in familial Parkinson's disease exhibits a weaker lipid‐binding property

Movement Disorders

Kensuke Daida

Shotaro Shimonaka

Kahori Shiba‐Fukushima

Jun Ogata

Hiroyo Yoshino

...

2022/10

Loss of Atg2b and Gskip Impairs the Maintenance of the Hematopoietic Stem Cell Pool Size

Molecular and Cellular Biology

Shun-suke Sakai

Atsushi Hasegawa

Ryosuke Ishimura

Naoki Tamura

Shun Kageyama

...

2022/1/1

Pathophysiological evaluation of the LRRK2 G2385R risk variant for Parkinson’s disease

npj Parkinson's Disease

Toshiki Tezuka

Daisuke Taniguchi

Mariko Sano

Tomoyo Shimada

Yutaka Oji

...

2022/8/5

The East Asian Parkinson disease genomics consortium

The Lancet Neurology

Kin Y Mok

East Asian Parkinson Disease Genomics Consortium

2021

Genetic analysis of ATP10B for Parkinson's disease in Japan

Parkinsonism & Related Disorders

Mayu Ishiguro

Hiroyo Yoshino

Yuanzhe Li

Aya Ikeda

Manabu Funayama

...

2021/7/1

Reply: PSAP intronic variants around saposin D domain and Parkinson’s disease

Brain

Yutaka Oji

Taku Hatano

Manabu Funayama

Nobutaka Hattori

2021/1/1

See List of Professors in Manabu Funayama University(Juntendo University)