Hope Twede

Scientist

Publications

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A Comparison of Wearable Tonometry, Photoplethysmography, and Electrocardiography for Cuffless Measurement of Blood Pressure in an Ambulatory Setting

Becky Mieloszyk, Hope Twede, Jonathan Lester, Jeremiah (Miah) Wander, Sumit Basu, Gabe Cohn, Greg Smith, Sidhant Gupta, Desney Tan, Nicolas Villar, Moni Wolf, Sailaja Malladi, Ron Paulsen, Scott Saponas

IEEE Journal of Biomedical and Health Informatics | July 2022, Vol 26(7): pp. 2864-2875

Publication
Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders.

Hope Twede

Neurology Genetics | November 2019, Vol 5(6)

DOI Publication

Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing.

Hope Twede

Scientific Reports | October 2019, Vol 9(1): pp. 15315

DOI Publication

Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.

Hope Twede

Journal of Neurodevelopmental Disorders | February 2019, Vol 11(1): pp. 3-3

DOI Publication
Clinical significance of copy number variants involving KANK1 in patients with neurodevelopmental disorders.

Hope Twede

European Journal of Medical Genetics | December 2018, Vol 62(1): pp. 15-20

DOI Publication

A survey of antiepileptic drug responses identifies drugs with potential efficacy for seizure control in Wolf–Hirschhorn syndrome

Hope Twede

Epilepsy & Behavior | March 2018, Vol 81: pp. 55-61

DOI Publication
Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.

Hope Twede

International Journal of Molecular Sciences | December 2016, Vol 17(12): pp. 2070

DOI Publication

Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.

Hope Twede

BioMed Research International | November 2016, Vol 2016: pp. 3284534-3284534

DOI Publication

A Comparison of Wearable Tonometry, Photoplethysmography, and Electrocardiography for Cuffless Measurement of Blood Pressure in an Ambulatory Setting

Becky Mieloszyk, Hope Twede, Jonathan Lester, Jeremiah (Miah) Wander, Sumit Basu, Gabe Cohn, Greg Smith, Sidhant Gupta, Desney Tan, Nicolas Villar, Moni Wolf, Sailaja Malladi, Ron Paulsen, Scott Saponas

IEEE Journal of Biomedical and Health Informatics | July 2022, Vol 26(7): pp. 2864-2875

Publication
A Comparison of Wearable Tonometry, Photoplethysmography, and Electrocardiography for Cuffless Measurement of Blood Pressure in an Ambulatory Setting

Becky Mieloszyk, Hope Twede, Jonathan Lester, Jeremiah (Miah) Wander, Sumit Basu, Gabe Cohn, Greg Smith, Sidhant Gupta, Desney Tan, Nicolas Villar, Moni Wolf, Sailaja Malladi, Ron Paulsen, Scott Saponas

IEEE Journal of Biomedical and Health Informatics | July 2022, Vol 26(7): pp. 2864-2875

Publication

Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders.

Hope Twede

Neurology Genetics | November 2019, Vol 5(6)

DOI Publication

Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing.

Hope Twede

Scientific Reports | October 2019, Vol 9(1): pp. 15315

DOI Publication

Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.

Hope Twede

Journal of Neurodevelopmental Disorders | February 2019, Vol 11(1): pp. 3-3

DOI Publication

Clinical significance of copy number variants involving KANK1 in patients with neurodevelopmental disorders.

Hope Twede

European Journal of Medical Genetics | December 2018, Vol 62(1): pp. 15-20

DOI Publication

A survey of antiepileptic drug responses identifies drugs with potential efficacy for seizure control in Wolf–Hirschhorn syndrome

Hope Twede

Epilepsy & Behavior | March 2018, Vol 81: pp. 55-61

DOI Publication

Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.

Hope Twede

International Journal of Molecular Sciences | December 2016, Vol 17(12): pp. 2070

DOI Publication

Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.

Hope Twede

BioMed Research International | November 2016, Vol 2016: pp. 3284534-3284534

DOI Publication

A Comparison of Wearable Tonometry, Photoplethysmography, and Electrocardiography for Cuffless Measurement of Blood Pressure in an Ambulatory Setting

Becky Mieloszyk, Hope Twede, Jonathan Lester, Jeremiah (Miah) Wander, Sumit Basu, Gabe Cohn, Greg Smith, Sidhant Gupta, Desney Tan, Nicolas Villar, Moni Wolf, Sailaja Malladi, Ron Paulsen, Scott Saponas

IEEE Journal of Biomedical and Health Informatics | July 2022, Vol 26(7): pp. 2864-2875

Publication

Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders.

Hope Twede

Neurology Genetics | November 2019, Vol 5(6)

DOI Publication

Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing.

Hope Twede

Scientific Reports | October 2019, Vol 9(1): pp. 15315

DOI Publication

Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.

Hope Twede

Journal of Neurodevelopmental Disorders | February 2019, Vol 11(1): pp. 3-3

DOI Publication

Clinical significance of copy number variants involving KANK1 in patients with neurodevelopmental disorders.

Hope Twede

European Journal of Medical Genetics | December 2018, Vol 62(1): pp. 15-20

DOI Publication

A survey of antiepileptic drug responses identifies drugs with potential efficacy for seizure control in Wolf–Hirschhorn syndrome

Hope Twede

Epilepsy & Behavior | March 2018, Vol 81: pp. 55-61

DOI Publication

Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.

Hope Twede

International Journal of Molecular Sciences | December 2016, Vol 17(12): pp. 2070

DOI Publication

Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.

Hope Twede

BioMed Research International | November 2016, Vol 2016: pp. 3284534-3284534

DOI Publication