Christine Patch | Academic Influence

Christine Patch's AcademicInfluence.com Rankings

Christine Patch

Computer Science

#11494

World Rank

#12185

Historical Rank

Machine Learning

#5530

World Rank

#5604

Historical Rank

Artificial Intelligence

#5971

World Rank

#6063

Historical Rank

Database

#9134

World Rank

#9605

Historical Rank

computer-science Degrees

Download Badge

Computer Science

Christine Patch's Degrees

PhD Computer Science Stanford University
Masters Computer Science University of California, Berkeley
Bachelors Computer Science University of California, Berkeley

Similar Degrees You Can Earn

Why Is Christine Patch Influential?

(Suggest an Edit or Addition)

According to Wikipedia, Christine Patch is a nurse and genetic counsellor. She is a Principal Staff Scientist in Genomic Counselling in the Society and Ethics Research group, part of Wellcome Connecting Science, based on the Wellcome Genome Campus. She is also the Clinical Lead for Genetic Counselling at Genomics England, and a former President of the European Society of Human Genetics.

(See a Problem?)

Christine Patch's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Mutational signature in colorectal cancer caused by genotoxic pks+E. coli (2020) (426)
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS (2018) (206)
Penetrance for copy number variants associated with schizophrenia. (2010) (138)
How can the evaluation of genetic tests be enhanced? Lessons learned from the ACCE framework and evaluating genetic tests in the United Kingdom (2005) (126)
Whole-genome sequencing reveals host factors underlying critical COVID-19 (2022) (120)
Use of antihypertensive medications and mortality of patients with autosomal dominant polycystic kidney disease: a population-based study. (2011) (92)
Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension (2017) (84)
The 100,000 Genomes Pilot on Rare Disease Diagnosis in Healthcare − A Preliminary Report (2021) (72)
Developing a policy for paediatric biobanks: principles for good practice (2012) (66)
Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities (2011) (66)
Genetic counselling in the era of genomic medicine (2018) (57)
Opportunistic genomic screening. Recommendations of the European Society of Human Genetics (2020) (56)
European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death (2019) (56)
Genetic horoscopes: is it all in the genes? Points for regulatory control of direct-to-consumer genetic testing (2009) (53)
Living a normal life in an extraordinary way: A systematic review investigating experiences of families of young people's transition into adulthood when affected by a genetic and chronic childhood condition. (2016) (53)
A systematic CRISPR screen defines mutational mechanisms underpinning signatures caused by replication errors and endogenous DNA damage (2021) (51)
Factors affecting the clinical use of non‐invasive prenatal testing: a mixed methods systematic review (2013) (44)
Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data? (2020) (43)
Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes (2018) (43)
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis (2020) (40)
Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery (2015) (36)
A Systematic Search for Uniparental Disomy in Carriers of Chromosome Translocations (1994) (34)
Communication about genetic testing with breast and ovarian cancer patients: a scoping review (2018) (33)
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases (2021) (33)
Genetic Testing and Common Disorders: How to Assess Relevance and Possibilities (2011) (32)
Recommendations for education and training of genetic nurses and counsellors in the United Kingdom. (1998) (32)
Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders (2016) (30)
Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project (2019) (29)
Background Document to the ESHG recommendations on genetic testing and common disorders (2011) (29)
The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors (2017) (29)
Genetic counselors and Genomic Counseling in the United Kingdom (2014) (28)
Building the Genetic Counsellor Profession in the United Kingdom: Two Decades of Growth and Development (2013) (28)
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (2021) (28)
Parents’ motivations, concerns and understanding of genome sequencing: a qualitative interview study (2020) (28)
Position statement on opportunistic genomic screening from the Association of Genetic Nurses and Counsellors (UK and Ireland) (2014) (27)
De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures (2018) (26)
DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration (2020) (26)
Using a community of practice to develop standards of practice and education for genetic counsellors in Europe (2010) (24)
Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8. (1994) (24)
Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries (2021) (23)
Comparison of genotypic and phenotypic strategies for population screening in hemochromatosis: Assessment of anxiety, depression, and perception of health (2005) (21)
Opening the “black box” of informed consent appointments for genome sequencing: a multisite observational study (2018) (20)
Direct to consumer genetic tests (2009) (19)
Genetic testing in intellectual disability psychiatry: Opinions and practices of UK child and intellectual disability psychiatrists (2017) (18)
Spectrum of mutational signatures in T-cell lymphoma reveals a key role for UV radiation in cutaneous T-cell lymphoma (2021) (18)
Genetic Counsellors: A Registration System to Assure Competence in Practice in the United Kingdom (2004) (18)
Psychosocial aspects of DNA testing for hereditary hemochromatosis in at-risk individuals: a systematic review. (2009) (17)
Towards equitable and trustworthy genomics research (2022) (16)
Return of individual research results from genomic research: A systematic review of stakeholder perspectives (2021) (16)
Diagnostic strategies using DNA testing for hereditary haemochromatosis in at-risk populations: a systematic review and economic evaluation. (2009) (15)
A Roadmap for Global Acceleration of Genomics Integration Across Nursing (2020) (15)
Genetics for Healthcare Professionals: A Lifestage Approach (2002) (15)
Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi-Family Discussion Groups (2016) (15)
Factors affecting the uptake of screening: a randomised controlled non-inferiority trial comparing a genotypic and a phenotypic strategy for screening for haemochromatosis. (2005) (15)
An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy (2021) (14)
A systematic review of the clinical validity and clinical utility of DNA testing for hereditary haemochromatosis type 1 in at-risk populations (2008) (14)
Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with dentatorubral and pallidoluysian atrophy (2004) (14)
Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications (2018) (14)
A Delphi study to determine the European core curriculum for Master programmes in genetic counselling (2013) (12)
The 'new genetics' and nursing: what does it have to do with me? (2000) (12)
Study of the relationship between Black men, culture and prostate cancer beliefs (2018) (12)
Point of View: An evolution from genetic counselling to genomic counselling. (2019) (10)
Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis (2021) (9)
A Maturity Matrix for Nurse Leaders to Facilitate and Benchmark Progress in Genomic Healthcare Policy, Infrastructure, Education, and Delivery (2020) (9)
Applied Genetics in Healthcare (2005) (8)
A decision analysis model for diagnostic strategies using DNA testing for hereditary haemochromatosis in at risk populations. (2008) (8)
Black and Minority Ethnic women's decision-making for risk reduction strategies after BRCA testing: Use of context and knowledge. (2019) (8)
Duplication of 10q24 locus: broadening the clinical and radiological spectrum (2019) (8)
Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland (2020) (8)
Advances in the genetics of schizophrenia: will high-risk copy number variants be useful in clinical genetics or diagnostics? (2009) (8)
Development and mixed-methods evaluation of an online animation for young people about genome sequencing (2020) (7)
Potential for diagnosis of infectious disease from the 100,000 Genomes Project Metagenomic Dataset: Recommendations for reporting results (2019) (7)
Newborn Screening Policy in the United Kingdom & the United States:Two Different Communities of Practice (2006) (7)
Whole genome sequencing for diagnosis of neurological repeat expansion disorders (2020) (7)
Should doctors have a legal duty to warn relatives of their genetic risks? (2019) (7)
Young people's understanding, attitudes and involvement in decision-making about genome sequencing for rare diseases: A qualitative study with participants in the UK 100,000 genomes project. (2020) (7)
Decision-making, attitudes, and understanding among patients and relatives invited to undergo genome sequencing in the 100,000 Genomes Project: A multisite survey study. (2021) (6)
The genetic counsellor role in the United Kingdom (2022) (6)
Expanded carrier screening tests currently on the commercial market (2014) (6)
Autosomal Recessive Inheritance (2019) (6)
SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile. (2022) (5)
Autosomal Dominant Inheritance (2019) (5)
Developing a National Newborn Genomes Program: An Approach Driven by Ethics, Engagement and Co-design (2022) (5)
Family communication about cystic fibrosis from the mother's perspective: an exploratory study (2007) (5)
Genetics for the Health Sciences: A Handbook for Clinical Healthcare (2009) (5)
A ploidy-agnostic method for estimating telomere length from whole genome sequencing data. (2018) (4)
Solving unsolved rare neurological diseases—a Solve-RD viewpoint (2021) (4)
Erratum: Patenting and licensing in genetic testing: Recommendations of the European Society of Human Genetics (European Journal of Human Genetics) (2008) vol. 16 (405-411) 10.1038/sj.ejhg.5201929) (2008) (3)
Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study (2022) (3)
ESHG PPPC Comments on postmortem use of genetic data for research purposes (2019) (3)
Development of a measure of genome sequencing knowledge for young people: The kids‐KOGS (2019) (3)
Engaged genomic science produces better and fairer outcomes: an engagement framework for engaging and involving participants, patients and publics in genomics research and healthcare implementation (2021) (3)
NHS Genomic Medicine Centres National Service Evaluation of the Consent Process and Participant Materials used in the 100,000 Genomes Project (2016) (3)
Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries. (2022) (3)
The family transition experience when living with childhood neuromuscular disease: A grounded theory study. (2021) (3)
Comparison of two screening strategies for haemochromatosis: a pilot study investigating uptake, feasibility and cost (2001) (2)
Interventions to improve patient access to and utilisation of genetic and genomic counselling services. (2015) (2)
The new genetics: A research agenda for nurses? (2002) (2)
Predictive or not predictive: understanding the mixed messages from the patient's DNA sequence. (2015) (2)
X-linked inheritance (2005) (2)
Co-designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom (2022) (1)
Prevalence and Burden of Disease in Hemochromatosis: Estimates Derived from Routine Data (2006) (1)
Feasibility and acceptability of two screening strategies for haemochromatosis, report of phase one of a randomised controlled trial. (2002) (1)
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol (2022) (1)
World congress on genetic counselling. (2019) (1)
Genetic screening for Hemochromatosis is no less acceptable than biochemical screening. (2003) (1)
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol [version 2; peer review: 3 approved, 1 approved with reservations] (2022) (1)
Mendelian gene identification through mouse embryo viability screening (2022) (1)
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans (2020) (1)
Multifactorial inheritance and common diseases (2005) (1)
Erratum : Direct to consumer genetic tests (European Journal of Human Genetics (2009) vol. 17 (1111) 10.1038/ejhg.2009.66) (2009) (1)
Identifying individuals who might benefit from genetic services and information. (2013) (1)
Genetics: is it part of your role? (2006) (1)
Basic cancer genetics (2014) (1)
Development and mixed-methods evaluation of an online animation for young people about genome sequencing (2020) (0)
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. (2021) (0)
Foundations in genetic science (2005) (0)
Genetic Counselling in Disorders of Low Penetrance (2010) (0)
Project Report - NHS Genomic Medicine Centres: Process and Participant Materials used in the 100,000 Genomes Project (2016) (0)
Becoming an adult : experiences of individuals affected by chronic childhood disease and their families during transition into adulthood - a systematic literature review (2015) (0)
Animation or leaflet: Does it make a difference when educating young people about genome sequencing? (2021) (0)
Whole genome sequencing reveals host factors underlying critical Covid-19 Accelerated Article Preview (2022) (0)
Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (2021) (0)
Correction to: Co‑designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom (2022) (0)
Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (2021) (0)
Duplication of 10q24 locus: broadening the clinical and radiological spectrum (2019) (0)
Working as an educator for families and professionals (2005) (0)
Impact of HFE mutations on a birth cohort aged 60. (2004) (0)
Living with a progressive neuromuscular disease : a grounded theory study of family experiences (2018) (0)
Working to support families (2005) (0)
Introduction to genetic healthcare (2005) (0)
Opportunities for poaching: using the public's enjoyment of popular culture to foster dialogues around genetics (2022) (0)
Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases (2021) (0)
A heartfelt "thank you" to all the reviewers of the Journal of Community Genetics in 2010 (2011) (0)
A comparison of a genetic screening strategy and a biochemical strategy for population screening for hemochromatosis (2005) (0)
Communication about genetic testing with breast and ovarian cancer patients: a scoping review (2018) (0)
Development of genetic services and the genetic counseling profession (2002) (0)
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol [version 1; peer review: 2 approved, 2 approved with reservations] (2021) (0)
Chromosomal and non-traditional patterns of inheritance (2005) (0)
Families living with neuromuscular diseases : the impact on family life (2018) (0)
Pregnancy and the perinatal period (2002) (0)
Psychosocial Aspects of DNA Testing for Hereditary Hemochromatosis in At-Risk Individuals: A Systematic Review (2009) (0)
Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries (2021) (0)
Second World Congress on Genetic Counseling: An introduction to the special issue (2021) (0)
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol [version 2; peer review: 2 approved, 2 approved with reservations] (2022) (0)
Haemochromatosis: the need for an agreed case definition. (2005) (0)
Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol [version 1; peer review: awaiting peer review] (2021) (0)
Working as a researcher (2005) (0)
“It didn’t mean anything” – moving within a landscape of knowledge to interpret genetics and genetic test results within familial cancer concerns (2021) (0)
Ethical Challenges Associated with Pathogen and Host Genetics in Infectious Disease (2022) (0)
Working practically in genetic healthcare (2005) (0)
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing (2023) (0)
Patient & public involvement for inherited cardiac conditions (2021) (0)
Family History (2020) (0)
Basic concepts in genetic science (2002) (0)
Reply to Blendis (2005) (0)
Childhood and adolescence (2002) (0)
Direct to consumer genetic tests (2009) (0)
A comparison of a genetic strategy and a biochemical strategy for population screening for haemochromatosis (2004) (0)
Working professionally in genetic healthcare (2005) (0)
Genetic testing for haemochromatosis: A survey of UK genetic centres (2000) (0)
Managing expectations, rights, and duties in large-scale genomics initiatives: a European comparison (2022) (0)
Opening the “black box” of informed consent appointments for genome sequencing: a multisite observational study (2018) (0)
Parents’ motivations, concerns and understanding of genome sequencing: a qualitative interview study (2020) (0)
Implications of Emerging Technologies for Genetic Counselling (2011) (0)

This paper list is powered by the following services:

Other Resources About Christine Patch

en.wikipedia.org

What Schools Are Affiliated With Christine Patch?

Christine Patch is affiliated with the following schools: