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Biocompatibility of trillium biopassive surface–coated oxygenator versus uncoated oxygenator during cardiopulmonary bypass

Journal of cardiothoracic and vascular anesthesia, 2001-10, Vol.15 (5), p.545-550

2001

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Lenalidomide (CC-5013) Treatment for Anemia Associated with Myelofibrosis with Myeloid Metaplasia

Blood, 2005-11, Vol.106 (11), p.2583-2583

2005

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A Phase II Study of CC-5013 Treatment for Myelofibrosis with Myeloid Metaplasia: A Preliminary Report

Blood, 2004-11, Vol.104 (11), p.1505-1505

2004

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Milestones of Lynch syndrome: 1895-2015

Nature reviews. Cancer, 2015-03, Vol.15 (3), p.181-194

2015

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Health literacy and the social determinants of health: a qualitative model from adult learners

Health promotion international, 2017-02, Vol.32 (1), p.130-138

2017

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Pulmonary response prediction through personalized basis functions in a virtual patient model

Computer methods and programs in biomedicine, 2024-02, Vol.244, p.107988-107988, Article 107988

2024

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Familial atypical multiple mole melanoma (FAMMM) syndrome: history, genetics, and heterogeneity

Familial cancer, 2016-07, Vol.15 (3), p.487-491

2016

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Analysis of the CDKN2A Gene in FAMMM Syndrome Families Reveals Early Age of Onset for Additional Syndromic Cancers

Cancer research (Chicago, Ill.), 2019-06, Vol.79 (11), p.2992-3000

2019

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Commentary on Almassalha et al., "The Greater Genomic Landscape: The Heterogeneous Evolution of Cancer"

Cancer research (Chicago, Ill.), 2016-10, Vol.76 (19), p.5602-5604

2016

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Implementation of a novel stratified PAthway of CarE for common musculoskeletal (MSK) conditions in primary care: protocol for a multicentre pragmatic randomised controlled trial (the PACE MSK trial)

BMJ open, 2021-12, Vol.11 (12), p.e057705-e057705

2021

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Analysis of selected maternal exposures and non-syndromic atrioventricular septal defects in the National Birth Defects Prevention Study, 1997-2005

American journal of medical genetics. Part A, 2012-10, Vol.158A (10), p.2447-2455

2012

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Abstract 2300: Deleterious germline mutations in the BRCA1 gene are associated with increased risk for cancers of the female reproductive system other than breast and ovarian as well as other cancers

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.2300-2300

2020

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Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications

European journal of human genetics : EJHG, 2006-04, Vol.14 (4), p.390-402

2006

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Maternal periconceptional occupational pesticide exposure and neural tube defects

Birth defects research. A Clinical and molecular teratology, 2014-11, Vol.100 (11), p.877-886

2014

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Absence of Damaging Effects of Stem Cell Donation in Unrelated Donors Assessed By FISH and Gene Variance Screening

Blood, 2019-11, Vol.134 (Supplement_1), p.4474-4474

2019

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Familial prostate cancer and HOXB13 founder mutations: geographic and racial/ethnic variations

Human genetics, 2013, Vol.132 (1), p.1-4

2013

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Screening for familial and hereditary prostate cancer

International journal of cancer, 2016-06, Vol.138 (11), p.2579-2591

2016

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Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge

Familial cancer, 2018-07, Vol.17 (3), p.403-414

2018

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Recurrent SARS-CoV-2 mutations in immunodeficient patients

Virus evolution, 2022-12, Vol.8 (2), p.veac050

2022

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The benefits of a model of interval comprehensive assessments (MICA) in hereditary cancer Syndromes: Hereditary diffuse gastric cancer (HDGC) as an example

Cancer genetics, 2019-04, Vol.233-234, p.43-47

2019

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“If we can do it, anyone can!”: Evaluating a virtual “Paper Chase” collaborative writing model for rapid research dissemination

Active learning in higher education, 2024-03, Vol.25 (1), p.115-134

2024

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Spatial growth rate of emerging SARS-CoV-2 lineages in England, September 2020–December 2021

Epidemiology and infection, 2022-07, Vol.150, p.e145-e145, Article e145

2022

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Major hereditary gastrointestinal cancer syndromes: a narrative review

Journal of gastrointestinal and liver diseases : JGLD, 2017-06, Vol.26 (2), p.157-163

2017

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Immune reconstitution following umbilical cord blood transplantation: IRES, a study of UK paediatric patients

EJHaem, 2020-07, Vol.1 (1), p.208-218

2020

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Communication and technology in genetic counseling for familial cancer

Clinical genetics, 2014-03, Vol.85 (3), p.213-222

2014

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Biocompatibility of trillium biopassive surface–coated oxygenator versus uncoated oxygenator during cardiopulmonary bypass

Lenalidomide (CC-5013) Treatment for Anemia Associated with Myelofibrosis with Myeloid Metaplasia

A Phase II Study of CC-5013 Treatment for Myelofibrosis with Myeloid Metaplasia: A Preliminary Report

Milestones of Lynch syndrome: 1895-2015

Health literacy and the social determinants of health: a qualitative model from adult learners

Pulmonary response prediction through personalized basis functions in a virtual patient model

Familial atypical multiple mole melanoma (FAMMM) syndrome: history, genetics, and heterogeneity

Analysis of the CDKN2A Gene in FAMMM Syndrome Families Reveals Early Age of Onset for Additional Syndromic Cancers

Commentary on Almassalha et al., "The Greater Genomic Landscape: The Heterogeneous Evolution of Cancer"

Implementation of a novel stratified PAthway of CarE for common musculoskeletal (MSK) conditions in primary care: protocol for a multicentre pragmatic randomised controlled trial (the PACE MSK trial)

Analysis of selected maternal exposures and non-syndromic atrioventricular septal defects in the National Birth Defects Prevention Study, 1997-2005

Abstract 2300: Deleterious germline mutations in the BRCA1 gene are associated with increased risk for cancers of the female reproductive system other than breast and ovarian as well as other cancers

Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications

Maternal periconceptional occupational pesticide exposure and neural tube defects

Absence of Damaging Effects of Stem Cell Donation in Unrelated Donors Assessed By FISH and Gene Variance Screening

Familial prostate cancer and HOXB13 founder mutations: geographic and racial/ethnic variations

Screening for familial and hereditary prostate cancer

Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge

Recurrent SARS-CoV-2 mutations in immunodeficient patients

The benefits of a model of interval comprehensive assessments (MICA) in hereditary cancer Syndromes: Hereditary diffuse gastric cancer (HDGC) as an example

“If we can do it, anyone can!”: Evaluating a virtual “Paper Chase” collaborative writing model for rapid research dissemination

Spatial growth rate of emerging SARS-CoV-2 lineages in England, September 2020–December 2021

Major hereditary gastrointestinal cancer syndromes: a narrative review

Immune reconstitution following umbilical cord blood transplantation: IRES, a study of UK paediatric patients

Communication and technology in genetic counseling for familial cancer

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