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Amendments and Corrections | 19 November 2020 | Open
Author Correction: Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form
- Huiming Yang
- , Su Yang
- , Liang Jing
- , Luoxiu Huang
- , Luxiao Chen
- , Xianxian Zhao
- , Weili Yang
- , Yongcheng Pan
- , Peng Yin
- , Zhaohui S Qin
- , Beisha Tang
- , Shihua Li
- & Xiao-Jiang Li
Nature Communications 11 , 1–1

Rights & permissionsfor article Author Correction: Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form . Opens in a new window.
Amendments and Corrections | 26 May 2020
Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes
- Andrea Cortese
- , Yi Zhu
- , Adriana P. Rebelo
- , Sara Negri
- , Steve Courel
- , Lisa Abreu
- , Chelsea J. Bacon
- , Yunhong Bai
- , Dana M. Bis-Brewer
- , Enrico Bugiardini
- , Elena Buglo
- , Matt C. Danzi
- , Shawna M. E. Feely
- , Alkyoni Athanasiou-Fragkouli
- , Nourelhoda A. Haridy
- , Aixa Rodriguez
- , Alexa Bacha
- , Ashley Kosikowski
- , Beth Wood
- , Brett McCray
- , Brianna Blume
- , Carly Siskind
- , Charlotte Sumner
- , Daniela Calabrese
- , David Walk
- , Dragan Vujovic
- , Eun Park
- , Francesco Muntoni
- , Gabrielle Donlevy
- , Gyula Acsadi
- , John Day
- , Joshua Burns
- , Jun Li
- , Karen Krajewski
- , Kate Eichinger
- , Kayla Cornett
- , Krista Mullen
- , Perez Quiros Laura
- , Laurie Gutmann
- , Maria Barrett
- , Mario Saporta
- , Mariola Skorupinska
- , Natalie Grant
- , Paula Bray
- , Reza Seyedsadjadi
- , Riccardo Zuccarino
- , Richard Finkel
- , Richard Lewis
- , Sabrina Yum
- , Sarah Hilbert
- , Simone Thomas
- , Steffen Behrens-Spraggins
- , Tara Jones
- , Thomas Lloyd
- , Tiffany Grider
- , Tim Estilow
- , Vera Fridman
- , Rosario Isasi
- , Alaa Khan
- , Matilde Laurà
- , Stefania Magri
- , Menelaos Pipis
- , Chiara Pisciotta
- , Eric Powell
- , Alexander M. Rossor
- , Paola Saveri
- , Janet E. Sowden
- , Stefano Tozza
- , Jana Vandrovcova
- , Julia Dallman
- , Elena Grignani
- , Enrico Marchioni
- , Steven S. Scherer
- , Beisha Tang
- , Zhiqiang Lin
- , Abdullah Al-Ajmi
- , Rebecca Schüle
- , Matthis Synofzik
- , Thierry Maisonobe
- , Tanya Stojkovic
- , Michaela Auer-Grumbach
- , Mohamed A. Abdelhamed
- , Sherifa A. Hamed
- , Ruxu Zhang
- , Fiore Manganelli
- , Lucio Santoro
- , Franco Taroni
- , Davide Pareyson
- , Henry Houlden
- , David N. Herrmann
- , Mary M. Reilly
- , Michael E. Shy
- , R. Grace Zhai
- & Stephan Zuchner
Nature Genetics 52 , 640–640

Rights & permissionsfor article Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes . Opens in a new window.
Research | 22 May 2020 | Open
Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form
- Huiming Yang
- , Su Yang
- , Liang Jing
- , Luoxiu Huang
- , Luxiao Chen
- , Xianxian Zhao
- , Weili Yang
- , Yongcheng Pan
- , Peng Yin
- , Zhaohui S Qin
- , Beisha Tang
- , Shihua Li
- & Xiao-Jiang Li
Nature Communications 11 , 1–15

Rights & permissionsfor article Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form . Opens in a new window.
Research | 18 June 2018
The genotypic and phenotypic spectrum of PARS2-related infantile-onset encephalopathy
- Xiaomeng Yin
- , Beisha Tang
- , Xiao Mao
- , Jinxin Peng
- , Sheng Zeng
- , Yaqin Wang
- , Hong Jiang
- & Nan Li
Journal of Human Genetics 63 , 971–980

Rights & permissionsfor article The genotypic and phenotypic spectrum of PARS2-related infantile-onset encephalopathy . Opens in a new window.
Research | 11 August 2017 | Open
Assessment of Three New Loci from Genome-wide Association Study in Essential Tremor in Chinese population
- Yuan Zhang
- , Yuwen Zhao
- , Xiaoting Zhou
- , Kai Li
- , Minhan Yi
- , Jifeng Guo
- , Xinxiang Yan
- , Beisha Tang
- & Qiying Sun
Scientific Reports 7 , 1–5

Rights & permissionsfor article Assessment of Three New Loci from Genome-wide Association Study in Essential Tremor in Chinese population . Opens in a new window.
Research | 9 May 2017 | Open
Novel mutations in ADSL for Adenylosuccinate Lyase Deficiency identified by the combination of Trio-WES and constantly updated guidelines
- Xiao Mao
- , Kai Li
- , Beisha Tang
- , Yang Luo
- , Dongxue Ding
- , Yuwen Zhao
- , Chunrong Wang
- , Xiaoting Zhou
- , Zhenhua Liu
- , Yuan Zhang
- , Puzhi Wang
- , Qian Xu
- , Qiying Sun
- , Kun Xia
- , Xinxiang Yan
- , Hong Jiang
- , Shen Lu
- & Jifeng Guo
Scientific Reports 7 , 1–7

Rights & permissionsfor article Novel mutations in ADSL for Adenylosuccinate Lyase Deficiency identified by the combination of Trio-WES and constantly updated guidelines . Opens in a new window.
Research | 4 May 2020
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes
- Andrea Cortese
- , Yi Zhu
- , Adriana P. Rebelo
- , Sara Negri
- , Steve Courel
- , Lisa Abreu
- , Chelsea J. Bacon
- , Yunhong Bai
- , Dana M. Bis-Brewer
- , Enrico Bugiardini
- , Elena Buglo
- , Matt C. Danzi
- , Shawna M. E. Feely
- , Alkyoni Athanasiou-Fragkouli
- , Nourelhoda A. Haridy
- , Aixa Rodriguez
- , Alexa Bacha
- , Ashley Kosikowski
- , Beth Wood
- , Brett McCray
- , Brianna Blume
- , Carly Siskind
- , Charlotte Sumner
- , Daniela Calabrese
- , David Walk
- , Dragan Vujovic
- , Eun Park
- , Francesco Muntoni
- , Gabrielle Donlevy
- , Gyula Acsadi
- , John Day
- , Joshua Burns
- , Jun Li
- , Karen Krajewski
- , Kate Eichinger
- , Kayla Cornett
- , Krista Mullen
- , Perez Quiros Laura
- , Laurie Gutmann
- , Maria Barrett
- , Mario Saporta
- , Mariola Skorupinska
- , Natalie Grant
- , Paula Bray
- , Reza Seyedsadjadi
- , Riccardo Zuccarino
- , Richard Finkel
- , Richard Lewis
- , Rosemary R. Shy
- , Sabrina Yum
- , Sarah Hilbert
- , Simone Thomas
- , Steffen Behrens-Spraggins
- , Tara Jones
- , Thomas Lloyd
- , Tiffany Grider
- , Tim Estilow
- , Vera Fridman
- , Rosario Isasi
- , Alaa Khan
- , Matilde Laurà
- , Stefania Magri
- , Menelaos Pipis
- , Chiara Pisciotta
- , Eric Powell
- , Alexander M. Rossor
- , Paola Saveri
- , Janet E. Sowden
- , Stefano Tozza
- , Jana Vandrovcova
- , Julia Dallman
- , Elena Grignani
- , Enrico Marchioni
- , Steven S. Scherer
- , Beisha Tang
- , Zhiqiang Lin
- , Abdullah Al-Ajmi
- , Rebecca Schüle
- , Matthis Synofzik
- , Thierry Maisonobe
- , Tanya Stojkovic
- , Michaela Auer-Grumbach
- , Mohamed A. Abdelhamed
- , Sherifa A. Hamed
- , Ruxu Zhang
- , Fiore Manganelli
- , Lucio Santoro
- , Franco Taroni
- , Davide Pareyson
- , Henry Houlden
- , David N. Herrmann
- , Mary M. Reilly
- , Michael E. Shy
- , R. Grace Zhai
- & Stephan Zuchner
Nature Genetics 52 , 473–481

Rights & permissionsfor article Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes . Opens in a new window.
Research | 2 February 2016 | Open
Lack of association between IL-10 and IL-18 gene promoter polymorphisms and Parkinson’s disease with cognitive impairment in a Chinese population
- Zhenhua Liu
- , Jifeng Guo
- , Yaqin Wang
- , Kai Li
- , Jifeng Kang
- , Yang Wei
- , Qiying Sun
- , Qian Xu
- , Changshui Xu
- , Xinxiang Yan
- & Beisha Tang
Scientific Reports 6 , 1–6

Rights & permissionsfor article Lack of association between IL-10 and IL-18 gene promoter polymorphisms and Parkinson’s disease with cognitive impairment in a Chinese population . Opens in a new window.
Research | 8 September 2016 | Open
Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China
- Lihua Hou
- , Bin Jiao
- , Tingting Xiao
- , Lu Zhou
- , Zhifan Zhou
- , Juan Du
- , Xinxiang Yan
- , Junling Wang
- , Beisha Tang
- & Lu Shen
Scientific Reports 6 , 1–7

Rights & permissionsfor article Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China . Opens in a new window.
Research | 24 October 2016 | Open
Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expression
- Yongcheng Pan
- , Lusi Zhang
- , Qiong Liu
- , Ying Li
- , Hui Guo
- , Yu Peng
- , Hexiang Peng
- , Beisha Tang
- , Zhengmao Hu
- , Jingping Zhao
- , Kun Xia
- & Jia-Da Li
Scientific Reports 6 , 1–8

Rights & permissionsfor article Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expression . Opens in a new window.
Research | 27 January 2016 | Open
Spinocerebellar ataxia type 21 exists in the Chinese Han population
- Sheng Zeng
- , Junsheng Zeng
- , Miao He
- , Xianfeng Zeng
- , Yao Zhou
- , Zhen Liu
- , Kun Xia
- , Qian Pan
- , Hong Jiang
- , Lu Shen
- , Xinxiang Yan
- , Beisha Tang
- & Junling Wang
Scientific Reports 6 , 1–4

Rights & permissionsfor article Spinocerebellar ataxia type 21 exists in the Chinese Han population . Opens in a new window.
Research | 5 February 2016 | Open
Identification of a de novo DYNC1H1 mutation via WES according to published guidelines
- Dongxue Ding
- , Zhao Chen
- , Kai Li
- , Zhe Long
- , Wei Ye
- , Zhaoli Tang
- , Kun Xia
- , Rong Qiu
- , Beisha Tang
- & Hong Jiang
Scientific Reports 6 , 1–5

Rights & permissionsfor article Identification of a de novo DYNC1H1 mutation via WES according to published guidelines . Opens in a new window.
Research | 2 December 2016 | Open
Mutational analysis of PRNP in Alzheimer’s disease and frontotemporal dementia in China
- Weiwei Zhang
- , Bin Jiao
- , Tingting Xiao
- , Chuzheng Pan
- , Xixi Liu
- , Lin Zhou
- , Beisha Tang
- & Lu Shen
Scientific Reports 6 , 1–7

Rights & permissionsfor article Mutational analysis of PRNP in Alzheimer’s disease and frontotemporal dementia in China . Opens in a new window.
Research | 12 February 2016 | Open
Prediction of orthostatic hypotension in multiple system atrophy and Parkinson disease
- Zhanfang Sun
- , Dandan Jia
- , Yuting Shi
- , Xuan Hou
- , Xiaosu Yang
- , Jifeng Guo
- , Nan Li
- , Junling Wang
- , Qiying Sun
- , Hainan Zhang
- , Lifang Lei
- , Lu Shen
- , Xinxiang Yan
- , Kun Xia
- , Hong Jiang
- & Beisha Tang
Scientific Reports 6 , 1–7

Rights & permissionsfor article Prediction of orthostatic hypotension in multiple system atrophy and Parkinson disease . Opens in a new window.
Research | 28 April 2013
Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis
- Min Deng
- , Ling Wei
- , Xianbo Zuo
- , Yanghua Tian
- , Fei Xie
- , Panpan Hu
- , Chunyan Zhu
- , Fengqiong Yu
- , Yu Meng
- , Honghao Wang
- , Fangfang Zhang
- , Huijuan Ma
- , Rong Ye
- , Huaidong Cheng
- , Jing Du
- , Wenwen Dong
- , Shanshan Zhou
- , Changqing Wang
- , Yu Wang
- , Jingye Wang
- , Xianwen Chen
- , Zhongwu Sun
- , Nong Zhou
- , Yubao Jiang
- , Xiuxiu Liu
- , Xiaogang Li
- , Nan Zhang
- , Na Liu
- , Yingjun Guan
- , Yongsheng Han
- , Yongzhu Han
- , Xinyi Lv
- , Yu Fu
- , Hui Yu
- , Chunhua Xi
- , Dandan Xie
- , Qiyuan Zhao
- , Peng Xie
- , Xin Wang
- , Zhijun Zhang
- , Lu Shen
- , Yong Cui
- , Xianyong Yin
- , Hui Cheng
- , Bo Liang
- , Xiaodong Zheng
- , Tatia M C Lee
- , Gang Chen
- , Fusheng Zhou
- , Jan H Veldink
- , Wim Robberecht
- , John E Landers
- , Peter M Andersen
- , Ammar Al-Chalabi
- , Chris Shaw
- , Chunfeng Liu
- , Beisha Tang
- , Shangxi Xiao
- , Janice Robertson
- , Fengyu Zhang
- , Leonard H van den Berg
- , Liangdan Sun
- , Jianjun Liu
- , Sen Yang
- , Xiaodong Ju
- , Kai Wang
- & Xuejun Zhang
Nature Genetics 45 , 697–700

Rights & permissionsfor article Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis . Opens in a new window.
Amendments and Corrections | 29 May 2013
Erratum: Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis
- Min Deng
- , Ling Wei
- , Xianbo Zuo
- , Yanghua Tian
- , Fei Xie
- , Panpan Hu
- , Chunyan Zhu
- , Fengqiong Yu
- , Yu Meng
- , Honghao Wang
- , Fangfang Zhang
- , Huijuan Ma
- , Rong Ye
- , Huaidong Cheng
- , Jing Du
- , Wenwen Dong
- , Shanshan Zhou
- , Changqing Wang
- , Yu Wang
- , Jingye Wang
- , Xianwen Chen
- , Zhongwu Sun
- , Nong Zhou
- , Yubao Jiang
- , Xiuxiu Liu
- , Xiaogang Li
- , Nan Zhang
- , Na Liu
- , Yingjun Guan
- , Yongsheng Han
- , Yongzhu Han
- , Xinyi Lv
- , Yu Fu
- , Hui Yu
- , Chunhua Xi
- , Dandan Xie
- , Qiyuan Zhao
- , Peng Xie
- , Xin Wang
- , Zhijun Zhang
- , Lu Shen
- , Yong Cui
- , Xianyong Yin
- , Hui Cheng
- , Bo Liang
- , Xiaodong Zheng
- , Tatia M C Lee
- , Gang Chen
- , Fusheng Zhou
- , Jan H Veldink
- , Wim Robberecht
- , John E Landers
- , Peter M Andersen
- , Ammar Al-Chalabi
- , Chris Shaw
- , Chunfeng Liu
- , Beisha Tang
- , Shangxi Xiao
- , Janice Robertson
- , Fengyu Zhang
- , Leonard H van den Berg
- , Liangdan Sun
- , Jianjun Liu
- , Sen Yang
- , Xiaodong Ju
- , Kai Wang
- & Xuejun Zhang
Nature Genetics 45 , 714–714

Rights & permissionsfor article Erratum: Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis . Opens in a new window.
5 March 2015
Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia
- Hui Guo
- , Ping Tong
- , Yanling Liu
- , Lu Xia
- , Tianyun Wang
- , Qi Tian
- , Ying Li
- , Yiqiao Hu
- , Yu Zheng
- , Xuemin Jin
- , Yunping Li
- , Wei Xiong
- , Beisha Tang
- , Yong Feng
- , Jiada Li
- , Qian Pan
- , Zhengmao Hu
- & Kun Xia
Genetics in Medicine 17 , 300–306

Rights & permissionsfor article Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia . Opens in a new window.
Research | 27 February 2020 | Open
Cerebellum-enriched protein INPP5A contributes to selective neuropathology in mouse model of spinocerebellar ataxias type 17
- Qiong Liu
- , Shanshan Huang
- , Peng Yin
- , Su Yang
- , Jennifer Zhang
- , Liang Jing
- , Siying Cheng
- , Beisha Tang
- , Xiao-Jiang Li
- , Yongcheng Pan
- & Shihua Li
Nature Communications 11 , 1–13

Rights & permissionsfor article Cerebellum-enriched protein INPP5A contributes to selective neuropathology in mouse model of spinocerebellar ataxias type 17 . Opens in a new window.
Research | 8 January 2015
Chinese homozygous Machado–Joseph disease (MJD)/SCA3: a case report
- Sheng Zeng
- , Junsheng Zeng
- , Miao He
- , Xianfeng Zeng
- , Yao Zhou
- , Zhen Liu
- , Hong Jiang
- , Beisha Tang
- & Junling Wang
Journal of Human Genetics 60 , 157–160

Rights & permissionsfor article Chinese homozygous Machado–Joseph disease (MJD)/SCA3: a case report . Opens in a new window.
Research | 18 June 2018
A presenilin-1 mutation causes Alzheimer disease without affecting Notch signaling
- Shuting Zhang
- , Fang Cai
- , Yili Wu
- , Tahereh Bozorgmehr
- , Zhe Wang
- , Si Zhang
- , Daochao Huang
- , Jifeng Guo
- , Lu Shen
- , Catharine Rankin
- , Beisha Tang
- & Weihong Song
Molecular Psychiatry 25 , 603–613

Rights & permissionsfor article A presenilin-1 mutation causes Alzheimer disease without affecting Notch signaling . Opens in a new window.
Research | 24 October 2017 | Open
DNA N6-methyladenine is dynamically regulated in the mouse brain following environmental stress
- Bing Yao
- , Ying Cheng
- , Zhiqin Wang
- , Yujing Li
- , Li Chen
- , Luoxiu Huang
- , Wenxin Zhang
- , Dahua Chen
- , Hao Wu
- , Beisha Tang
- & Peng Jin
Nature Communications 8 , 1–10

Rights & permissionsfor article DNA N6-methyladenine is dynamically regulated in the mouse brain following environmental stress . Opens in a new window.
Research | 1 June 2017 | Open
Cystatin C as a potential therapeutic mediator against Parkinson’s disease via VEGF-induced angiogenesis and enhanced neuronal autophagy in neurovascular units
- Jing Zou
- , Zhaoyu Chen
- , Xiaobo Wei
- , Zhigang Chen
- , Yongmei Fu
- , Xiaoyan Yang
- , Dan Chen
- , Rui Wang
- , Peter Jenner
- , Jia-Hong Lu
- , Min Li
- , Zhuohua Zhang
- , Beisha Tang
- , Kunlin Jin
- & Qing Wang
Cell Death & Disease 8 , e2854–e2854

Rights & permissionsfor article Cystatin C as a potential therapeutic mediator against Parkinson’s disease via VEGF-induced angiogenesis and enhanced neuronal autophagy in neurovascular units . Opens in a new window.
Research | 29 September 2016 | Open
Nur77 exacerbates PC12 cellular injury in vitro by aggravating mitochondrial impairment and endoplasmic reticulum stress
- Huimin Gao
- , Zhaoyu Chen
- , Yongmei Fu
- , Xiaoyan Yang
- , Ruihui Weng
- , Rui Wang
- , Jianjun Lu
- , Mengqiu Pan
- , Kunlin Jin
- , Chris McElroy
- , Beisha Tang
- , Ying Xia
- & Qing Wang
Scientific Reports 6 , 1–14

Rights & permissionsfor article Nur77 exacerbates PC12 cellular injury in vitro by aggravating mitochondrial impairment and endoplasmic reticulum stress . Opens in a new window.
Research | 6 June 2016
Identification of TMEM230 mutations in familial Parkinson's disease
- Han-Xiang Deng
- , Yong Shi
- , Yi Yang
- , Kreshnik B Ahmeti
- , Nimrod Miller
- , Cao Huang
- , Lijun Cheng
- , Hong Zhai
- , Sheng Deng
- , Karen Nuytemans
- , Nicola J Corbett
- , Myung Jong Kim
- , Hao Deng
- , Beisha Tang
- , Ziquang Yang
- , Yanming Xu
- , Piu Chan
- , Bo Huang
- , Xiao-Ping Gao
- , Zhi Song
- , Zhenhua Liu
- , Faisal Fecto
- , Nailah Siddique
- , Tatiana Foroud
- , Joseph Jankovic
- , Bernardino Ghetti
- , Daniel A Nicholson
- , Dimitri Krainc
- , Onur Melen
- , Jeffery M Vance
- , Margaret A Pericak-Vance
- , Yong-Chao Ma
- , Ali H Rajput
- & Teepu Siddique
Nature Genetics 48 , 733–739

Rights & permissionsfor article Identification of TMEM230 mutations in familial Parkinson's disease . Opens in a new window.
Research | 3 February 2016 | Open
Estrogen receptor-α is localized to neurofibrillary tangles in Alzheimer’s disease
- Chunyu Wang
- , Fan Zhang
- , Sirui Jiang
- , Sandra L. Siedlak
- , Lu Shen
- , George Perry
- , Xinglong Wang
- , Beisha Tang
- & Xiongwei Zhu
Scientific Reports 6 , 1–10

Rights & permissionsfor article Estrogen receptor-α is localized to neurofibrillary tangles in Alzheimer’s disease . Opens in a new window.
Research | 20 September 2016 | Open
Combined Diffusion Tensor Imaging and Arterial Spin Labeling as Markers of Early Parkinson’s disease
- Xiaobo Wei
- , Ronghua Yan
- , Zhaoyu Chen
- , Ruihui Weng
- , Xu Liu
- , Huimin Gao
- , Xiaofeng Xu
- , Zhuang Kang
- , Zhexing Liu
- , Yan Guo
- , Zhenhua Liu
- , Jan Petter Larsen
- , Jin Wang
- , Beisha Tang
- , Mark Hallett
- & Qing Wang
Scientific Reports 6 , 1–10

Rights & permissionsfor article Combined Diffusion Tensor Imaging and Arterial Spin Labeling as Markers of Early Parkinson’s disease . Opens in a new window.
Research | 6 July 2016 | Open
Genome-wide analysis of DNA methylation during antagonism of DMOG to MnCl2-induced cytotoxicity in the mouse substantia nigra
- Nannan Yang
- , Yang Wei
- , Tan Wang
- , Jifeng Guo
- , Qiying Sun
- , Yacen Hu
- , Xinxiang Yan
- , Xiongwei Zhu
- , Beisha Tang
- & Qian Xu
Scientific Reports 6 , 1–10

Rights & permissionsfor article Genome-wide analysis of DNA methylation during antagonism of DMOG to MnCl2-induced cytotoxicity in the mouse substantia nigra . Opens in a new window.

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Author Correction: Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form

Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form

The genotypic and phenotypic spectrum of PARS2-related infantile-onset encephalopathy

Assessment of Three New Loci from Genome-wide Association Study in Essential Tremor in Chinese population

Novel mutations in ADSL for Adenylosuccinate Lyase Deficiency identified by the combination of Trio-WES and constantly updated guidelines

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Lack of association between IL-10 and IL-18 gene promoter polymorphisms and Parkinson’s disease with cognitive impairment in a Chinese population

Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China

Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expression

Spinocerebellar ataxia type 21 exists in the Chinese Han population

Identification of a de novo DYNC1H1 mutation via WES according to published guidelines

Mutational analysis of PRNP in Alzheimer’s disease and frontotemporal dementia in China

Prediction of orthostatic hypotension in multiple system atrophy and Parkinson disease

Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis

Erratum: Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis

Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia

Cerebellum-enriched protein INPP5A contributes to selective neuropathology in mouse model of spinocerebellar ataxias type 17

Chinese homozygous Machado–Joseph disease (MJD)/SCA3: a case report

A presenilin-1 mutation causes Alzheimer disease without affecting Notch signaling

DNA N6-methyladenine is dynamically regulated in the mouse brain following environmental stress

Cystatin C as a potential therapeutic mediator against Parkinson’s disease via VEGF-induced angiogenesis and enhanced neuronal autophagy in neurovascular units

Nur77 exacerbates PC12 cellular injury in vitro by aggravating mitochondrial impairment and endoplasmic reticulum stress

Identification of TMEM230 mutations in familial Parkinson's disease

Estrogen receptor-α is localized to neurofibrillary tangles in Alzheimer’s disease

Combined Diffusion Tensor Imaging and Arterial Spin Labeling as Markers of Early Parkinson’s disease

Genome-wide analysis of DNA methylation during antagonism of DMOG to MnCl2-induced cytotoxicity in the mouse substantia nigra

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