Bar-Shira Anat相关文献与解析，生知库 | 链接生命科学的每一步

Droby, Amgad; Yoffe-Vasiliev, Avital; Atias, Daniel; Fraser, Kyle B; Mabrouk, Omar S; Omer, Nurit; Bar-Shira, Anat; Gana-Weisz, Mali; Goldstein, Orly; Artzi, Moran; Ben Bashat, Dafna; Alcalay, Roy N; Orr-Urtreger, Avi; Shirvan, Julia C; Cedarbaum, Jesse M; Giladi, Nir; Mirelman, Anat; Thaler, Avner

帕金森

神经科学

发表日期：2025

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Effect of GBA1 Mutations and APOE Polymorphisms on Survival and Progression Among Ashkenazi Jews with Dementia with Lewy Bodies

GBA1基因突变和APOE基因多态性对患有路易体痴呆症的德系犹太人的生存和疾病进展的影响

期刊:Movement Disorders

影响因子:7.6

doi:10.1002/mds.30003

Shiner, Tamara; Kavé, Gitit; Mirelman, Anat; Regev, Keren; Piura, Yoav; Goldstein, Orly; Gana Weisz, Mali; Bar-Shira, Anat; Gurevich, Tanya; Orr-Urtreger, Avi; Alcalay, Roy N; Giladi, Nir; Bregman, Noa

APOE

发表日期：2024

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MAPT Locus in Parkinson's Disease Patients of Ashkenazi Origin: A Stratified Analysis

阿什肯纳兹犹太人帕金森病患者的MAPT基因位点：一项分层分析

期刊:Genes

影响因子:2.8

doi:10.3390/genes15010046

Shani, Shachar; Gana-Weisz, Mali; Bar-Shira, Anat; Thaler, Avner; Gurevich, Tanya; Mirelman, Anat; Giladi, Nir; Alcalay, Roy N; Goldstein, Orly; Orr-Urtreger, Avi

Mutations in GBA and LRRK2 Are Not Associated with Increased Inflammatory Markers.

GBA 和 LRRK2 基因突变与炎症标志物增加无关

期刊:Journal of Parkinsons Disease

影响因子:5

doi:10.3233/JPD-212624

Thaler Avner, Omer Nurit, Giladi Nir, Gurevich Tanya, Bar-Shira Anat, Gana-Weisz Mali, Goldstein Orly, Kestenbaum Meir, Shirvan Julia C, Cedarbaum Jesse M, Orr-Urtreger Avi, Regev Keren, Shenhar-Tsarfaty Shani, Mirelman Anat

Deletion in COL4A2 is associated with a three-generation variable phenotype: from fetal to adult manifestations

COL4A2基因缺失与三代可变表型相关：从胎儿期到成人期均有表现。

期刊:European Journal of Human Genetics

影响因子:4.6

doi:10.1038/s41431-021-00880-3

Hausman-Kedem, Moran; Ben-Sira, Liat; Kidron, Debora; Ben-Shachar, Shay; Straussberg, Rachel; Marom, Daphna; Ponger, Penina; Bar-Shira, Anat; Malinger, Gustavo; Fattal-Valevski, Aviva

COL

发表日期：2021

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The Effect of GBA Mutations and APOE Polymorphisms on Dementia with Lewy Bodies in Ashkenazi Jews

GBA基因突变和APOE基因多态性对阿什肯纳兹犹太人路易体痴呆症的影响

期刊:Journal of Alzheimers Disease

影响因子:3.1

doi:10.3233/JAD-201295

Shiner, Tamara; Mirelman, Anat; Rosenblum, Yevgenia; Kavé, Gitit; Weisz, Mali Gana; Bar-Shira, Anat; Goldstein, Orly; Thaler, Avner; Gurevich, Tanya; Orr-Urtreger, Avi; Giladi, Nir; Bregman, Noa

APOE

发表日期：2021

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C9orf72-G(4)C(2) Intermediate Repeats and Parkinson's Disease; A Data-Driven Hypothesis

C9orf72-G(4)C(2)中间重复序列与帕金森病：一项数据驱动的假设

期刊:Genes

影响因子:2.8

doi:10.3390/genes12081210

Kobo, Hila; Goldstein, Orly; Gana-Weisz, Mali; Bar-Shira, Anat; Gurevich, Tanya; Thaler, Avner; Mirelman, Anat; Giladi, Nir; Orr-Urtreger, Avi

Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers

在健康 G2019S-LRRK2 携带者中应用运动障碍协会前驱症状标准

期刊:Movement Disorders

影响因子:7.6

doi:10.1002/mds.27342

Mirelman, Anat; Saunders-Pullman, Rachel; Alcalay, Roy N; Shustak, Shiran; Thaler, Avner; Gurevich, Tanya; Raymond, Deborah; Mejia-Santana, Helen; Orbe Reilly, Martha; Ozelius, Laurie; Clark, Lorraine; Gana-Weisz, Mali; Bar-Shira, Anat; Orr-Utreger, Avi; Bressman, Susan B; Marder, Karen; Giladi, Nir

LRRK2

发表日期：2018

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High frequency of C9orf72 hexanucleotide repeat expansion in amyotrophic lateral sclerosis patients from two founder populations sharing the same risk haplotype

在两个具有相同风险单倍型的创始人群中，肌萎缩侧索硬化症患者中C9orf72六核苷酸重复扩增的频率很高

期刊:Neurobiology of Aging

影响因子:3.5

doi:10.1016/j.neurobiolaging.2017.12.015

Goldstein, Orly; Gana-Weisz, Mali; Nefussy, Beatrice; Vainer, Batel; Nayshool, Omri; Bar-Shira, Anat; Traynor, Bryan J; Drory, Vivian E; Orr-Urtreger, Avi

发表日期：2018

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Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene

携带LRRK2基因G2019S突变的健康阿什肯纳兹犹太人的非运动症状

期刊:Movement Disorders

影响因子:7.6

doi:10.1002/mds.26213

Mirelman, Anat; Alcalay, Roy N; Saunders-Pullman, Rachel; Yasinovsky, Kira; Thaler, Avner; Gurevich, Tanya; Mejia-Santana, Helen; Raymond, Deborah; Gana-Weisz, Mali; Bar-Shira, Anat; Ozelius, Laurie; Clark, Lorraine; Orr-Urtreger, Avi; Bressman, Susan; Marder, Karen; Giladi, Nir

LRRK2

发表日期：2015

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Radiological markers of CSF α-synuclein aggregation in Parkinson's disease patients

帕金森病患者脑脊液α-突触核蛋白聚集的放射学标志物

Effect of GBA1 Mutations and APOE Polymorphisms on Survival and Progression Among Ashkenazi Jews with Dementia with Lewy Bodies

GBA1基因突变和APOE基因多态性对患有路易体痴呆症的德系犹太人的生存和疾病进展的影响

MAPT Locus in Parkinson's Disease Patients of Ashkenazi Origin: A Stratified Analysis

阿什肯纳兹犹太人帕金森病患者的MAPT基因位点：一项分层分析

Mutations in GBA and LRRK2 Are Not Associated with Increased Inflammatory Markers.

GBA 和 LRRK2 基因突变与炎症标志物增加无关

Deletion in COL4A2 is associated with a three-generation variable phenotype: from fetal to adult manifestations

COL4A2基因缺失与三代可变表型相关：从胎儿期到成人期均有表现。

The Effect of GBA Mutations and APOE Polymorphisms on Dementia with Lewy Bodies in Ashkenazi Jews

GBA基因突变和APOE基因多态性对阿什肯纳兹犹太人路易体痴呆症的影响

C9orf72-G(4)C(2) Intermediate Repeats and Parkinson's Disease; A Data-Driven Hypothesis

C9orf72-G(4)C(2)中间重复序列与帕金森病：一项数据驱动的假设

Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers

在健康 G2019S-LRRK2 携带者中应用运动障碍协会前驱症状标准

High frequency of C9orf72 hexanucleotide repeat expansion in amyotrophic lateral sclerosis patients from two founder populations sharing the same risk haplotype

在两个具有相同风险单倍型的创始人群中，肌萎缩侧索硬化症患者中C9orf72六核苷酸重复扩增的频率很高

Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene

携带LRRK2基因G2019S突变的健康阿什肯纳兹犹太人的非运动症状