Christine Patch

Also affiliated with Maastricht University, Wellcome Connecting Science, Genomics England, William Harvey Research Institute

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

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 17 papers. Top paper: “Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli”.

Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli

Nature(2020)10.1038/s41586-020-2080-8

N/A

8.3DataRank · unranked

1184 citations

Jens Puschhof, Axel Rosendahl Huber, Arne van Hoeck, Henry M. Wood, Jason Nomburg +95 more

An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy

Brain(2020)10.1093/brain/awaa420

N/A

0DataRank · unranked

56 citations

Rauan Kaiyrzhanov, Yaqun Zou, Sahar Da’as, Reza Maroofian, Sandra Donkervoort +91 more

A Maturity Matrix for Nurse Leaders to Facilitate and Benchmark Progress in Genomic Healthcare Policy, Infrastructure, Education, and Delivery

Journal of Nursing Scholarship(2020)10.1111/jnu.12586

N/A

0DataRank · unranked

32 citations

Kathleen A. Calzone, Laurie Badzek, Caroline Benjamin, Anna Middleton, Christine Patch +2 more

A Roadmap for Global Acceleration of Genomics Integration Across Nursing

Journal of Nursing Scholarship(2020)10.1111/jnu.12552

N/A

0DataRank · unranked

56 citations

Kathleen A. Calzone, Laurie Badzek, Caroline Benjamin, Anna Middleton, Christine Patch +2 more

Return of individual research results from genomic research: A systematic review of stakeholder perspectives

PLoS ONE(2021)10.1371/journal.pone.0258646

N/A

0DataRank · unranked

78 citations

Joel T. Minion, Stephanie Roberts, James Cummings, Mavis Machirori, Mwenza Blell +13 more

Correspondence on “Ensuring best practice in genomics education and evaluation: Reporting item standards for education and its evaluation in genomics (RISE2 Genomics)” by Nisselle et al

Genetics in Medicine(2021)10.1016/j.gim.2021.11.023

N/A

0DataRank · unranked

2 citations

Kathleen A. Calzone, Sarah Dewell, Laurie Badzek, Christine Patch, Andrew Dwyer

Return of individual research results from genomic research: A systematic review of stakeholder perspectives.

DOAJ (DOAJ: Directory of Open Access Journals)(2021)10.17863/cam.77899

N/A

0DataRank · unranked

0 citations

Joel T. Minion, Stephanie Roberts, Cummings, James, Mavis Machirori, Mwenza Blell +13 more

Whole-genome sequencing reveals host factors underlying critical COVID-19

Nature(2022)10.1038/s41586-022-04576-6

N/A

0DataRank · unranked

350 citations

Erola Pairo-Castineira, Konrad Rawlik, A. Stuckey, Christopher A. Odhams, Susan Walker +84 more

Towards equitable and trustworthy genomics research

EBioMedicine(2022)10.1016/j.ebiom.2022.103879

N/A

0DataRank · unranked

72 citations

Richard Milne, Alesia Costa, Christine Patch, Anna Middleton, Jerome Atutornu

SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile

Genetics in Medicine(2022)10.1016/j.gim.2022.02.013

N/A

0DataRank · unranked

36 citations

Aidin Foroutan, Jennifer Kerkhof, Haley McConkey, Michael A. Levy, Sadegheh Haghshenas +95 more

Mendelian gene identification through mouse embryo viability screening

Genome Medicine(2022)10.1186/s13073-022-01118-7

N/A

0DataRank · unranked

15 citations

Carl Henrik Westerberg, Jesse Mager, Mary E. Dickinson, Lauryl M. J. Nutter, Violeta Muñoz‐Fuentes +95 more

Identification of 4 novel human ocular coloboma genes ANK3, BMPR1B, PDGFRA, and CDH4 through evolutionary conserved vertebrate gene analysis

Genetics in Medicine(2022)10.1016/j.gim.2021.12.014

N/A

0DataRank · unranked

13 citations

Maria Toms, Rodrigo Young, Jonathan Eintracht, Hajrah Sarkar, Brian P. Brooks +70 more

Normal and pathogenic variation of RFC1 repeat expansions: implications for clinical diagnosis

Brain(2023)10.1093/brain/awad240

N/A

0DataRank · unranked

72 citations

Stefania Magri, Riccardo Curró, Elena Abati, Stefano Facchini, Marinella Corbetta +95 more

Current State of Genomics in Nursing: A Scoping Review of Healthcare Provider Oriented (Clinical and Educational) Outcomes (2012–2022)

Genes(2023)10.3390/genes14112013

N/A

0DataRank · unranked

58 citations

Jordan Keels, Kathleen A. Calzone, Laurie Badzek, Sarah Dewell, Christine Patch +3 more

The genomic landscape of familial glioma

Science Advances(2023)10.1126/sciadv.ade2675

N/A

0DataRank · unranked

50 citations

Georgina Armstrong, Brittney Lozzi, Prashanth Vijayaraghavan, Sharon E. Plon, Terence C. Wong +85 more

Unexpected frequency of the pathogenic AR CAG repeat expansion in the general population

Brain(2023)10.1093/brain/awad050

N/A

0DataRank · unranked

28 citations

Kristina Ibáñez, Anna‐Leigh Brown, Prasanth Sivakumar, Alessandro Bombaci, Liana Santos +94 more

The impact of a secondary, rare, non-pathogenic PKD1 variant on disease progression in autosomal dominant polycystic kidney disease

Journal of Nephrology(2025)10.1007/s40620-025-02211-x

N/A

0DataRank · unranked

0 citations

Kane E. Collins, Sophia Heneghan, Edmund Gilbert, Hana Yang, Sarah R. Senum +82 more