Michelle A. Ramos

发表

New Mitochondrial Disease Identified In Monozygotic Twin Boys

V. Jobanputra, R. Happle, B. Gelb, 2023, American journal of medical genetics. Part A.

GUÍA: a digital platform to facilitate result disclosure in genetic counseling

G. Bertier, B. Gelb, E. Kenny, 2020, Genetics in Medicine.

Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program

V. Jobanputra, A. Abhyankar, B. Gelb, 2023, Clinical genetics.

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

V. Jobanputra, A. Abhyankar, B. Gelb, 2023, medRxiv.

Detection of mosaic variants using genome sequencing in a large pediatric cohort

V. Jobanputra, B. Gelb, E. Kenny, 2022, American journal of medical genetics. Part A.

Successful recruitment and retention of diverse participants in a genomics clinical trial: a good invitation to a great party

L. Richardson, C. Horowitz, M. Ramos, 2019, Genetics in Medicine.

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families

B. Gelb, E. Kenny, J. Greally, 2023, medRxiv.

The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing

V. Jobanputra, C. Cunningham-Rundles, B. Gelb, 2023, Pilot and Feasibility Studies.

Integration of stakeholder engagement from development to dissemination in genomic medicine research: Approaches and outcomes from the CSER Consortium.

Ebony B Madden, Ebony B. Madden, Kathleen F. Mittendorf, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

Siobhan M. Dolan, V. Jobanputra, T. Bloom, 2020, Trials.

Are Parental Perceptions of Child Activity Levels and Overall Health More Important than Perceptions of Weight?

Ashley M. Fox, L. Kleinman, M. Galvez, 2016, Maternal and Child Health Journal.

Implementing a pragmatic clinical trial to tailor opioids for acute pain on behalf of the IGNITE ADOPT PGx investigators

S. Volpi, D. Voora, P. Dexter, 2022, Clinical and translational science.

Views Of Primary Care Providers On Testing Patients For Genetic Risks For Common Chronic Diseases.

C. Horowitz, M. Ramos, D. Hauser, 2018, Health affairs.

Determining the effects and challenges of incorporating genetic testing into primary care management of hypertensive patients with African ancestry.

Rennie Negron, E. Bottinger, N. Abul-Husn, 2016, Contemporary clinical trials.

Lessons learned about harmonizing survey measures for the CSER consortium

K. Goddard, L. Hindorff, A. McGuire, 2020, Journal of clinical and translational science.

Correction to: The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

Siobhan M. Dolan, V. Jobanputra, T. Bloom, 2021, Trials.

Opportunities to implement a sustainable genomic medicine program: lessons learned from the IGNITE Network

Ebony B Madden, Ebony B. Madden, G. Ginsburg, 2018, Genetics in Medicine.

Developing a Common Framework for Evaluating the Implementation of Genomic Medicine Interventions in Clinical Care: The IGNITE Network’s Common Measures Working Group

Ebony B Madden, Ebony B. Madden, C. Voils, 2017, Genetics in Medicine.

Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals

Ebony B Madden, Ebony B. Madden, E. Bottinger, 2022, JAMA network open.

Translating pharmacogenetics from research to routine clinical practice – a survey of the IGNITE Network

Ebony B Madden, Ebony B. Madden, G. Ginsburg, 2020, Translational Medicine Communications.

Establishing the Value of Genomics in Medicine – The IGNITE Pragmatic Trials Network

Ebony B Madden, Henry H. Ong, Ebony B. Madden, 2021, Genetics in Medicine.

A Community-Engaged Approach to Select Geographic Areas for Interventions to Reduce Health Disparities

L. Kleinman, E. Cromley, C. Horowitz, 2011, Progress in community health partnerships : research, education, and action.

Comprehensive examination of the multilevel adverse risk and protective factors for cardiovascular disease among hypertensive African Americans

L. Richardson, G. Ogedegbe, A. Schoenthaler, 2019, Journal of clinical hypertension.

Barriers to Physical Activity in East Harlem, New York

Ashley M. Fox, D. Mann, L. Kleinman, 2012, Journal of obesity.

Creating accessible Spanish language materials for Clinical Sequencing Evidence-Generating Research consortium genomic projects: challenges and lessons learned.

Kathleen F. Mittendorf, N. Lindberg, Frank A Angelo, 2021, Personalized medicine.

Strategies to Integrate Genomic Medicine into Clinical Care: Evidence from the IGNITE Network

Henry H. Ong, G. Ginsburg, P. Dexter, 2021, Journal of personalized medicine.

The relationship between alexithymia and perinatal depressive symptomatology.

R. Muñoz, H. Le, M. Ramos, 2007, Journal of psychosomatic research.