Bryan J. Traynor

Also affiliated with Johns Hopkins University, University Medical Center, National Institute on Aging

MedicineNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 2%percentile

2.1Author DataRank

Indexed papers

4in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 4 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort

Neurology(2020)10.1212/wnl.0000000000011209

Top 19%

1.1DataRank

Top 19%40 citations

Andrea Calvo, Cristina Moglia, Maura Brunetti, Marco Barberis, Luca Sbaiz +14 more

Papers

Driven by 78 papers — median percentile 71. Top paper: “Large-scale rare variant burden testing in Parkinson's disease”.

Large-scale rare variant burden testing in Parkinson's disease

Brain(2023)10.1093/brain/awad214

N/A

1.4DataRank · unranked

52 citations

Julie Lake, Vanessa Pitz, Allen Ye Fu, Joseph L. Guidubaldi, Caroline Warly Solsberg +31 more

Identification of a pathogenic intronic KIF5A mutation in an ALS-FTD kindred

Neurology(2020)10.1212/wnl.0000000000011064

N/A

1.1DataRank · unranked

32 citations

Clifton L. Dalgard, Jinhui Ding, Adriano Chiò, Camile Alba, Dan N. Hupalo +6 more

Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort

Neurology(2020)10.1212/wnl.0000000000011209

Top 19%

1.1DataRank

Top 19%40 citations

Andrea Calvo, Cristina Moglia, Maura Brunetti, Marco Barberis, Luca Sbaiz +14 more

The Overlapping Genetics of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia

Frontiers in Neuroscience(2020)10.3389/fnins.2020.00042

N/A

0.825DataRank · unranked

243 citations

Pietro Fratta, Bryan J. Traynor, Ruth Chia, Yevgeniya Abramzon

Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation

Nature Methods(2023)10.1038/s41592-023-01993-x

N/A

0.747DataRank · unranked

144 citations

Kimberley J. Billingsley, Mira Mastoras, Melissa Meredith, Jean Monlong, Ryan Lorig-Roach +25 more

Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study

The Lancet Neurology(2020)10.1016/s1474-4422(20)30394-x

N/A

0.719DataRank · unranked

120 citations

Shunsuke Koga, Rebecca R. Valentino, Regina Hertfelder Reynolds, Raffaele Ferrari, Manuela Tan +51 more

Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease

Acta Neuropathologica(2020)10.1007/s00401-020-02181-3

N/A

0.718DataRank · unranked

119 citations

Sara Sáez-Atiénzar, Jeff Kim, Mary B. Makarious, Faraz Faghri, Mónica Díez-Fairén +23 more

ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of function

Cell Reports(2022)10.1016/j.celrep.2022.110598

N/A

0.700DataRank · unranked

105 citations

Adam R. Fenton, Sara Sáez-Atiénzar, Anthony Giampetruzzi, Aparna Sreeram, Shankaracharya +15 more

Exploring the phenotype of Italian patients with ALS with intermediateATXN2polyQ repeats

Journal of Neurology Neurosurgery & Psychiatry(2022)10.1136/jnnp-2022-329376

Top 29%

0.689DataRank

Top 29%18 citations

Cristina Moglia, Antonio Canosa, Umberto Manera, Maurizio Grassano, Rosario Vasta +16 more

NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations

medRxiv(2023)10.1101/2023.11.06.23298176

N/A

0.658DataRank · unranked

23 citations

Faraz Faghri, Elisa Majounie, Mathew J. Koretsky, Jeffrey Kim, Kristin Levine +29 more

TDP-43 loss induces cryptic polyadenylation in ALS/FTD

Nature Neuroscience(2025)10.1038/s41593-025-02050-w

N/A

0.593DataRank · unranked

23 citations

Anna‐Leigh Brown, Max Z. Y. J. Chien, Dario Dattilo, Puja R. Mehta, Francesca Mattedi +94 more

A fluid biomarker reveals loss of TDP-43 splicing repression in pre-symptomatic ALS

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.23.525202

N/A

0.553DataRank · unranked

39 citations

Pei Jasin, Kerstin E. Braunstein, Irika R. Sinha, Kyra D. Bowden, Abhay Moghekar +8 more

NeuroBooster Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations

Movement Disorders(2024)10.1002/mds.29902

N/A

0.550DataRank · unranked

38 citations

Faraz Faghri, Elisa Majounie, Mathew J. Koretsky, Jeffrey Kim, Kristin Levine +29 more

Genome‐Wide Analysis of Structural Variants in Parkinson Disease

Annals of Neurology(2023)10.1002/ana.26608

N/A

0.546DataRank · unranked

37 citations

Jinhui Ding, Pilar Álvarez Jerez, Anastasia Illarionova, Kristin Levine, Francis P. Grenn +35 more

Roadmap for C9ORF72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis: Report on the C9ORF72 FTD/ALS Summit

Neurology and Therapy(2023)10.1007/s40120-023-00548-8

N/A

0.533DataRank · unranked

34 citations

Bryan J. Traynor, Janice Robertson, Ludo Van Den Bosch, Sami J. Barmada, Clive N. Svendsen +49 more

Phenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral Sclerosis

Neurology Genetics(2022)10.1212/nxg.0000000000200011

N/A

0.524DataRank · unranked

32 citations

Giorgia Brodini, Giovanni De Marco, Federico Casale, Giuseppe Fuda, Paolina Salamone +13 more

A plasma proteomics-based candidate biomarker panel predictive of amyotrophic lateral sclerosis

Nature Medicine(2025)10.1038/s41591-025-03890-6

N/A

0.524DataRank · unranked

32 citations

Ruin Moaddel, Justin Kwan, Memoona Rasheed, Paola Ruffo, Natalie Landeck +35 more

Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.12.523790

N/A

0.520DataRank · unranked

31 citations

Kimberley J. Billingsley, Mira Mastoras, Melissa Meredith, Jean Monlong, Ryan Lorig-Roach +25 more

Advancements in genetic research and RNA therapy strategies for amyotrophic lateral sclerosis (ALS): current progress and future prospects

Journal of Neurology(2025)10.1007/s00415-025-12975-8

N/A

0.505DataRank · unranked

28 citations

Bryan J. Traynor, F. L. Conforti, Paola Ruffo

Nuclear depletion of RNA-binding protein ELAVL3 (HuC) in sporadic and familial amyotrophic lateral sclerosis

Acta Neuropathologica(2021)10.1007/s00401-021-02374-4

N/A

0.500DataRank · unranked

27 citations

Vivian I. Ko, Sonia Vazquez‐Sanchez, Ruth Chia, Olubankole Aladesuyi Arogundade, María José Gómez-Rodríguez +4 more

Combined epigenetic/genetic study identified an ALS age of onset modifier

Acta Neuropathologica Communications(2021)10.1186/s40478-021-01183-w

N/A

0.470DataRank · unranked

22 citations

Zhengrui Xi, Sara Sáez-Atiénzar, Ruth Chia, Danielle Moreno, Christine Sato +5 more

Novel TARDBP Sequence Variant and C9ORF72 Repeat Expansion in a Family With Frontotemporal Dementia

Alzheimer Disease & Associated Disorders(2014)10.1097/wad.0b013e318266fae5

N/A

0.457DataRank · unranked

20 citations

Virpi Moilanen, Marko Kervinen, Alan E. Renton, Bryan J. Traynor, Kari Majamaa +2 more

Genetic analysis of the X chromosome in people with Lewy body dementia nominates new risk loci

npj Parkinson s Disease(2024)10.1038/s41531-024-00649-7

N/A

0.406DataRank · unranked

14 citations

Paolo Reho, Irene Litvan, Jinhui Ding, J. Raphael Gibbs, Clifton L. Dalgard +4 more

Investigation of the genetic aetiology of Lewy body diseases with and without dementia

Brain Communications(2024)10.1093/braincomms/fcae190

N/A

0.385DataRank · unranked

12 citations

Raquel Real, Alejandro Martínez-Carrasco, Ruth Chia, Michael Lawton, Maryam Shoai +93 more

Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome

Annals of Neurology(2024)10.1002/ana.27040

N/A

0.385DataRank · unranked

12 citations

Ruth Chia, Sara Sáez-Atiénzar, Paola Ruffo, Memoona Rasheed, Jay P. Ross +7 more

C9orf72 Hexanucleotide Repeat in Huntington-Like Patients: Systematic Review and Meta-Analysis

Frontiers in Genetics(2020)10.3389/fgene.2020.551780

N/A

0.360DataRank · unranked

10 citations

Christoper A. Alarcón-Ruiz, Kevin Pacheco‐Barrios, Nicanor Mori, Josmel Pacheco‐Mendoza, Bryan J. Traynor +5 more

Profiling the NOTCH2NLC GGC Repeat Expansion in Parkinson's Disease in the European Population

Movement Disorders(2022)10.1002/mds.29155

N/A

0.312DataRank · unranked

7 citations

Pilar Álvarez Jerez, Francis P. Grenn, Sara Bandrés‐Ciga, Laksh Malik, Dena Hernandez +16 more

Differential methylation analysis in neuropathologically confirmed dementia with Lewy bodies

Communications Biology(2024)10.1038/s42003-023-05725-x

Top 55%

0.300DataRank

Top 55%6 citations

Sara Sáez-Atiénzar, Paola Ruffo, Sultana Solaiman, Zalak Shah, Ruth Chia +19 more

Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data

Cell Genomics(2024)10.1016/j.xgen.2024.100679

N/A

0.292DataRank · unranked

6 citations

Cleide Dos Santos Souza, Ruth Chia, Selina N. Beal, Ileana Lorenzini, Ruili Huang +92 more

Association of cardiovascular disease management drugs with Lewy body dementia: a case–control study

Brain Communications(2023)10.1093/braincomms/fcad346

N/A

0.292DataRank · unranked

6 citations

Brian Moroz, Sara Sáez-Atiénzar, Ruth Chia, Elizabeth K. Cahoon, Clifton L. Dalgard +93 more

Large-scale pathway-specific polygenic risk, transcriptomic community networks and functional inferences in Parkinson disease

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.05.079228

N/A

0.208DataRank · unranked

3 citations

Sara Sáez-Atiénzar, JJ Kim, MB Makarious, Faraz Faghri, Mónica Díez-Fairén +21 more

IntermediateHTTCAG repeats worsen disease severity in amyotrophic lateral sclerosis

Journal of Neurology Neurosurgery & Psychiatry(2024)10.1136/jnnp-2024-333998

N/A

0.208DataRank · unranked

3 citations

Antonio Canosa, Sandra D'Alfonso, Lucia Corrado, Giorgia Brodini, Emanuele Koumantakis +17 more

KIF5Ap.Pro986Leu Risk Variant and Accelerated Progression of Amyotrophic Lateral Sclerosis

Annals of Clinical and Translational Neurology(2025)10.1002/acn3.70059

N/A

0.165DataRank · unranked

2 citations

Rosario Vasta, Alberto Brusati, Francesco Scheveger, Silvia Peverelli, Alessio Maranzano +20 more

Identification and prediction of ALS subgroups using machine learning

medRxiv(2021)10.1101/2021.04.02.21254844

N/A

0.165DataRank · unranked

2 citations

Fabian Brunn, Anant Dadu, PARALS, ERRALS, Elisabetta Zucchi +12 more

The interneuron hypothesis of amyotrophic lateral sclerosis

Brain(2025)10.1093/brain/awaf104

N/A

0.104DataRank · unranked

1 citations

Bryan J. Traynor

Characterization of DNA methylation in PBMCs and donor-matched iPSCs shows methylation is reset during stem cell reprogramming

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.12.13.627515

N/A

0.104DataRank · unranked

1 citations

Cory A. Weller, Sara Sáez-Atiénzar, Alexandra Beilina, Sultana Solaiman, Makayla Portley +10 more

Investigation of the genetic aetiology of Lewy body diseases with and without dementia

medRxiv(2023)10.1101/2023.10.17.23297157

N/A

0.104DataRank · unranked

1 citations

Raquel Real, Alejandro Martínez-Carrasco, Ruth Chia, Michael Lawton, Maryam Shoai +14 more

Reply to Zhu et al.: Implications of CHRNB1 and ERBB2 in the pathobiology of myasthenia gravis

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2209096119

N/A

0DataRank · unranked

5 citations

Sara Sáez-Atiénzar, Daniel B. Drachman, Bryan J. Traynor, Ruth Chia

Personality traits are consistently associated with blood mitochondrial DNA copy number estimated from genome sequences in two genetic cohort studies

medRxiv(2022)10.1101/2022.06.04.22275970

N/A

0DataRank · unranked

2 citations

Antonio Terracciano, Martin Picard, Yong Qian, Thomas Bütler, Toshiko Tanaka +14 more

Cumulative genetic risk and C9orf72 repeat status independently associate with ALS status in two case-control studies

medRxiv(2022)10.1101/2022.10.27.22281377

N/A

0DataRank · unranked

0 citations

Kelly M. Bakulski, Kai Guo, Junguk Hur, Lili Zhou, Sara Sáez-Atiénzar +35 more

Reply: More than a co-incidence? Exploring the increased frequency of amyotrophic lateral sclerosis in Huntington disease

Acta Neuropathologica(2022)10.1007/s00401-022-02532-2

N/A

0DataRank · unranked

0 citations

Bryan J. Traynor, Karen Marder, Jean‐Paul Vonsattel, Richard A. Hickman

Amyotrophic lateral sclerosis: translating genetic discoveries into therapies

Nature Reviews Genetics(2023)10.1038/s41576-023-00592-y

N/A

0DataRank · unranked

219 citations

Elia R. Lopez, John E. Landers, Avindra Nath, Adriano Chiò, Ruth Chia +2 more

Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2108672119

N/A

0DataRank · unranked

133 citations

Sara Sáez-Atiénzar, Natalie A. Murphy, Adriano Chiò, Cornelis Blauwendraat, Ricardo H. Roda +48 more

Nuclear depletion of RNA binding protein ELAVL3 (HuC) in sporadic and familial amyotrophic lateral sclerosis

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.03.446017

N/A

0DataRank · unranked

6 citations

Vivian I. Ko, Sonia Vazquez‐Sanchez, Ruth Chia, Olubankole Aladesuyi Arogundade, María José Gómez-Rodríguez +4 more

Nature meets nurture in amyotrophic lateral sclerosis

The Lancet Neurology(2021)10.1016/s1474-4422(21)00097-1

N/A

0DataRank · unranked

1 citations

Andrea Calvo, Bryan J. Traynor, Adriano Chiò

Clinical testing panels for ALS: global distribution, consistency, and challenges

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration(2023)10.1080/21678421.2023.2173015

N/A

0DataRank · unranked

17 citations

Ahmad Al Nasser, Marwa Elnagheeb, Jennifer A. Fifita, Lyndal Henden, Ingrid M. Keseler +33 more

Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies

Neurology Genetics(2023)10.1212/nxg.0000000000200079

N/A

0DataRank · unranked

14 citations

Kelly M. Bakulski, Kai Guo, Junguk Hur, Lili Zhao, Sara Sáez-Atiénzar +36 more

Association of Copresence of Pathogenic Variants Related to Amyotrophic Lateral Sclerosis and Prognosis

Neurology(2023)10.1212/wnl.0000000000207367

N/A

0DataRank · unranked

13 citations

Cristina Moglia, Antonio Canosa, Umberto Manera, Maurizio Grassano, Rosario Vasta +16 more

Cognitive determinants of decisional capacity in neurodegenerative disorders

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51871

N/A

0DataRank · unranked

4 citations

Carolyn Sherer, Tianxia Wu, Jennifer Farren, Laura E. Danielian, Sonja W. Scholz +6 more

GBA variants influence cognitive status in amyotrophic lateral sclerosis

Journal of Neurology Neurosurgery & Psychiatry(2021)10.1136/jnnp-2021-327426

N/A

0DataRank · unranked

5 citations

Maurizio Grassano, Cristina Moglia, Barbara Iazzolino, Laura Peotta, Salvatore Gallone +14 more

Plasma microRNA signature as biomarker for disease progression in frontotemporal dementia and amyotrophic lateral sclerosis

Journal of Neurology Neurosurgery & Psychiatry(2021)10.1136/jnnp-2020-325478

N/A

0DataRank · unranked

5 citations

Bryan J. Traynor, Ramita Dewan

Highlighting the clinical potential of HTT repeat expansions in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Neuron(2021)10.1016/j.neuron.2021.04.020

N/A

0DataRank · unranked

7 citations

Sonja W. Scholz, Adriano Chiò, Bryan J. Traynor, Ramita Dewan

Investigating RFC1 expansions in sporadic amyotrophic lateral sclerosis

Journal of the Neurological Sciences(2021)10.1016/j.jns.2021.118061

N/A

0DataRank · unranked

14 citations

Ramita Dewan, Andrea Cortese, Susan M. Resnick, Luigi Ferrucci, Henry Houlden +2 more

Genomic analysis identifies risk factors in restless legs syndrome

medRxiv(2023)10.1101/2023.12.19.23300211

N/A

0DataRank · unranked

3 citations

Ruth Chia, Sara Sáez-Atiénzar, Paola Ruffo, Memoona Rasheed, Jay P. Ross +7 more

A fluid biomarker reveals loss of TDP-43 splicing repression in presymptomatic ALS–FTD

Nature Medicine(2024)10.1038/s41591-023-02788-5

N/A

0DataRank · unranked

150 citations

Pei Jasin, Kerstin E. Braunstein, Irika R. Sinha, Mark A. Garret, Kyra D. Bowden +12 more

Prognostic relationship of neurofilaments, CHIT1, YKL-40 and MCP-1 in amyotrophic lateral sclerosis

Journal of Neurology Neurosurgery & Psychiatry(2021)10.1136/jnnp-2021-327877

N/A

0DataRank · unranked

18 citations

Maxim De Schaepdryver, Mary Kay Floeter, Joke De Vocht, Nikita Lamaire, Ann D’Hondt +4 more

Epigenetic age acceleration is associated with occupational exposures, sex, and survival in amyotrophic lateral sclerosis

EBioMedicine(2024)10.1016/j.ebiom.2024.105383

N/A

0DataRank · unranked

18 citations

Xiayan Li, Kai Wang, Gayatri Iyer, Stacey A. Sakowski, Lili Zhao +10 more

Amyotrophic lateral sclerosis is over-represented in two Huntington’s disease brain bank cohorts: further evidence to support genetic pleiotropy of pathogenic HTT gene expansion

Acta Neuropathologica(2021)10.1007/s00401-021-02385-1

N/A

0DataRank · unranked

18 citations

Ramita Dewan, Etty Cortés, Bryan J. Traynor, Karen Marder, Jean‐Paul Vonsattel +1 more

Defective cyclophilin A induces TDP-43 proteinopathy: implications for amyotrophic lateral sclerosis and frontotemporal dementia

Brain(2021)10.1093/brain/awab333

N/A

0DataRank · unranked

32 citations

Maurizio Grassano, Silvia Pozzi, Silvia Luotti, Eliana Sammali, Alice Migazzi +16 more

Unraveling the complex interplay between genes, environment, and climate in ALS

EBioMedicine(2021)10.1016/j.ebiom.2021.103795

N/A

0DataRank · unranked

80 citations

Ruth Chia, Bryan J. Traynor, Adriano Chiò, Rosario Vasta

Therapeutic development approaches to treat haploinsufficiency diseases: restoring protein levels

Drug Discovery Today(2024)10.1016/j.drudis.2024.104201

N/A

0DataRank · unranked

8 citations

Zeenat A. Shyr, Bryan J. Traynor, Wei Zheng, Elena F Evans

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

JAMA Neurology(2021)10.1001/jamaneurol.2021.2598

N/A

0DataRank · unranked

85 citations

Ruth Chia, Danny E. Miller, Rachel Li, Ravindran Kumaran, Yevgeniya Abramzon +87 more

Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types

Science Advances(2021)10.1126/sciadv.abd9036

N/A

0DataRank · unranked

100 citations

Sara Bandrés‐Ciga, Rebekah G. Langston, Jonggeol J. Kim, Shing Wan Choi, Regina Hertfelder Reynolds +12 more

From use of omics to systems biology: Identifying therapeutic targets for amyotrophic lateral sclerosis

International review of neurobiology(2024)10.1016/bs.irn.2024.02.001

N/A

0DataRank · unranked

4 citations

Rosario Vasta, Scott P. Allen, Rachel Waller, Adriano Chiò, Bryan J. Traynor +2 more

Dominant mutations of the Notch ligand Jagged1 cause peripheral neuropathy

Journal of Clinical Investigation(2020)10.1172/jci128152

N/A

0DataRank · unranked

24 citations

William W. Motley, Janel O. Johnson, William H. Aisenberg, Katherine Marshall, Katy Barwick +16 more

Defective cyclophilin A induces TDP-43 proteinopathy: implications for amyotrophic lateral sclerosis and frontotemporal dementia

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.08.129528

N/A

0DataRank · unranked

2 citations

Maurizio Grassano, Silvia Pozzi, Silvia Luotti, Eliana Sammali, Alice Migazzi +16 more

Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.20.211276

N/A

0DataRank · unranked

9 citations

Sara Bandrés‐Ciga, Rebekah G. Langston, Jonggeol J. Kim, Shing Wan Choi, Regina Hertfelder Reynolds +11 more

Generation of two induced pluripotent stem cell (iPSC) lines from an ALS patient with simultaneous mutations in KIF5A and MATR3 genes

Stem Cell Research(2020)10.1016/j.scr.2020.102141

N/A

0DataRank · unranked

1 citations

Ashley Boehringer, Marissa Dominick, Ileana Lorenzini, Sara Sáez-Atiénzar, Erik P. Pioro +4 more

Unveiling the regulatory potential of the non-coding genome: Insights from the human genome project to precision medicine

Genes & Diseases(2025)10.1016/j.gendis.2025.101652

N/A

0DataRank · unranked

9 citations

Bryan J. Traynor, F. L. Conforti, Paola Ruffo

Gene expression signatures from whole blood predict amyotrophic lateral sclerosis case status and survival

Nature Communications(2025)10.1038/s41467-025-64622-5

N/A

0DataRank · unranked

4 citations

Masha G. Savelieff, Xiayan Li, Kai Guo, Kai Wang, Minghua Li +15 more

FUS Mislocalization Rewires a Cortical Gene Network to Drive Cognitive and Behavioral Impairment in ALS

medRxiv(2025)10.1101/2025.06.16.25329673

N/A

0DataRank · unranked

3 citations

Félicie Lorenc, Aurélie Bombardier, Claudia De Tapia, Stéphane Dieterle, Cláudio Gouveia Roque +17 more

Integrating a motor domain enhances disease severity scales in an FTD‐ALS spectrum cohort

Alzheimer s & Dementia(2025)10.1002/alz.70786

N/A

0DataRank · unranked

0 citations

Kiran Samra, Tianxia Wu, Lucy L. Russell, Jennifer Farren, Jody Crook +13 more

Personality traits are consistently associated with blood mitochondrial DNA copy number estimated from genome sequences in two genetic cohort studies

eLife(2022)10.7554/elife.77806

N/A

0DataRank · unranked

16 citations

Antonio Terracciano, Martin Picard, Yong Qian, Thomas Bütler, Toshiko Tanaka +14 more

ATXN2 intermediate expansions in amyotrophic lateral sclerosis

Brain(2022)10.1093/brain/awac167

N/A

0DataRank · unranked

48 citations

Ramita Dewan, Jinhui Ding, J. Raphael Gibbs, Clifton L. Dalgard, Pamela Keagle +6 more

Systematic evaluation of genetic mutations in ALS: a population-based study

Journal of Neurology Neurosurgery & Psychiatry(2022)10.1136/jnnp-2022-328931

N/A

0DataRank · unranked

62 citations

Andrea Calvo, Cristina Moglia, Luca Sbaiz, Maura Brunetti, Marco Barberis +13 more

The Neurogenetics Collection: emerging themes and future considerations for the field in Brain

Brain(2022)10.1093/brain/awac120

N/A

0DataRank · unranked

4 citations

Ammar Al‐Chalabi, Bryan J. Traynor

CAG Somatic Instability in a Huntington Disease Expansion Carrier Presenting with a Progressive Supranuclear Palsy‐like Phenotype

Movement Disorders(2022)10.1002/mds.29035

N/A

0DataRank · unranked

4 citations

Zane Jaunmuktane, Monica Emili Garcia‐Segura, Catherine Strand, Edward J. Wild, Joaquín Villar +5 more

G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlation

Neurobiology of Aging(2022)10.1016/j.neurobiolaging.2022.05.006

N/A

0DataRank · unranked

4 citations

Elisabetta Zucchi, Viviana Pensato, Cinzia Gellera, Bryan J. Traynor, Giulia Gianferrari +3 more

Bryan J. Traynor

Indexed papers

Top data-sharing exemplar

Papers