Nigel Williams

Biochemistry, Genetics and Molecular BiologyMedicine

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 100%percentile

0Author DataRank

Indexed papers

2in 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 2 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 →

Papers

Driven by 22 papers. Top paper: “Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets”.

Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets

JAMA Neurology(2021)10.1001/jamaneurol.2020.5257

N/A

4.5DataRank · unranked

205 citations

David Zhang, Sebastian Guelfi, Claudia Manzoni, Leon Hubbard, Regina Hertfelder Reynolds +85 more

Genome‐Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease

Movement Disorders(2020)10.1002/mds.28342

N/A

4.5DataRank · unranked

173 citations

Michael Lawton, Edwin Jabbari, Regina Hertfelder Reynolds, Hirotaka Iwaki, Cornelis Blauwendraat +23 more

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Cell Genomics(2023)10.1016/j.xgen.2023.100356

N/A

1.0DataRank · unranked

43 citations

Maxwell A. Sherman, Giulio Genovese, Thomas G. Gilgenast, Tushar Kamath, S.J. Burris +95 more

Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome

Nature Communications(2021)10.1038/s41467-021-26280-1

N/A

0.808DataRank · unranked

217 citations

Demis A. Kia, Mona M. Almramhi, Sara Bandres-Ciga, Chris Finan, Alastair J. Noyce +170 more

Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD

American Journal of Psychiatry(2012)10.1176/appi.ajp.2011.11040551

N/A

0.790DataRank · unranked

193 citations

Marian Hamshere, Peter Holmans, Kate Langley, Irina Zaharieva, Ziarah Hawi +7 more

Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1

npj Genomic Medicine(2022)10.1038/s41525-022-00317-w

N/A

0.649DataRank · unranked

21 citations

Branduff McAllister, Mia McDade‐Kumar, G. Bernhard Landwehrmeyer, Michael Orth, Anne Rosser +13 more

Genotype–phenotype correlation in PRKN-associated Parkinson’s disease

npj Parkinson s Disease(2024)10.1038/s41531-024-00677-3

N/A

0.612DataRank · unranked

58 citations

Sara Sambin, Baptiste Crinière‐Boizet, Thomas Courtin, Christelle Tesson, Fanny Casse +49 more

Genome-wide determinants of mortality and motor progression in Parkinson’s disease

npj Parkinson s Disease(2024)10.1038/s41531-024-00729-8

N/A

0.565DataRank · unranked

15 citations

Michael Lawton, Miriam I. Pollard, Emmeline Brown, Raquel Real, Alejandro Martínez-Carrasco +35 more

Genetic meta-analysis of levodopa induced dyskinesia in Parkinson’s disease

npj Parkinson s Disease(2023)10.1038/s41531-023-00573-2

N/A

0.489DataRank · unranked

13 citations

Raquel Real, Michael Lawton, Hirotaka Iwaki, Manuela Tan, Lesley Wu +11 more

Genome-wide association studies of cognitive and motor progression in Parkinson's disease

medRxiv(2020)10.1101/2020.05.07.20084343

N/A

0.464DataRank · unranked

21 citations

Michael Lawton, Edwin Jabbari, Regina Hertfelder Reynolds, Hirotaka Iwaki, Cornelis Blauwendraat +23 more

Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia

Molecular Psychiatry(2023)10.1038/s41380-023-02009-y

N/A

0.311DataRank · unranked

5 citations

Yingjie Zhao, M. Reza Jabalameli, Nha Nguyen, Joydeep Mitra, Ann Swillen +15 more

Genetic meta-analysis of levodopa induced dyskinesia in Parkinson’s disease

medRxiv(2023)10.1101/2023.05.24.23290362

N/A

0.165DataRank · unranked

2 citations

Raquel Real, Michael Lawton, Hirotaka Iwaki, Manuela Tan, Lesley Wu +11 more

ASSESSING THE RELATIONSHIP BETWEEN MONOALLELIC PARK2 MUTATIONS AND PARKINSON’S RISK

medRxiv(2020)10.1101/2020.06.26.20138172

N/A

0.149DataRank · unranked

1 citations

Bernabé I. Bustos, Jing Hu, Dimitri Krainc, Theresita Joseph, Jason Hehir +8 more

Association of genetic variation at the GJA5/ACP6 locus with motor progression in Parkinson’s

medRxiv(2022)10.1101/2022.10.28.22281645

N/A

0.117DataRank · unranked

1 citations

Raquel Real, Michael Lawton, Regina Hertfelder Reynolds, Manuela Tan, Lesley Wu +11 more

Association between the LRP1B and APOE loci and the development of Parkinson’s disease dementia

medRxiv(2022)10.1101/2022.05.23.22275465

N/A

0.104DataRank · unranked

1 citations

Alejandro Martínez-Carrasco, Regina Hertfelder Reynolds, Michael Lawton, Manuela Tan, Maryam Shoai +16 more

Epigenetic insights into neuropsychiatric and cognitive symptoms in Parkinson’s disease: A DNA co-methylation network analysis

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.07.20.549825

N/A

0.104DataRank · unranked

1 citations

Adam R. Smith, Luke Weymouth, Rebecca G. Smith, Isabel Castanho, Leon Hubbard +6 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

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

UCL Discovery (University College London)(2020)10.17615/snbr-qh40

N/A

0DataRank · unranked

0 citations

Kung‐Yee Liang, Per Hoffman, Stefan Herms, Gary Donohoe, Luba Kalaydjieva +94 more

Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset

Nature Neuroscience(2022)10.1038/s41593-022-01033-5

N/A

0DataRank · unranked

92 citations

Jasmine Donaldson, Caroline S. Binda, Sophie Powell, Uroosa Chughtai, Gareth Edwards +29 more

Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.16.452643

N/A

0DataRank · unranked

1 citations

Branduff McAllister, Mia McDade‐Kumar, G. Bernhard Landwehrmeyer, Michael Orth, Anne Rosser +13 more

Epigenetic insights into neuropsychiatric and cognitive symptoms in Parkinson's disease: A DNA co-methylation network analysis

Research Square(2023)10.21203/rs.3.rs-3185734/v1

N/A

0DataRank · unranked

4 citations

Joshua Harvey, Adam R. Smith, Luke Weymouth, Rebecca G. Smith, Isabel Castanho +6 more

FAN1 nuclease activity affects CAG expansion and age at onset of Huntington’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.13.439716

N/A

0DataRank · unranked

3 citations

Jasmine Donaldson, Caroline S. Binda, Sophie Powell, Uroosa Chughtai, Gareth Edwards +29 more