Hope Twede

Scientist

출판물

자료 보기:

- The Evidence Aggregator: AI reasoning applied to rare disease diagnostics
  
  Hope Twede, Lynn Pais, S. Bryen, Emily O’Heir, Greg Smith, Ron Paulsen, C. Austin-Tse, A. Bloemendal, C. Simons, Amanda K. Hall, Scott Saponas, Jeremiah (Miah) Wander, Daniel G. MacArthur, Heidi L. Rehm, Ashley Conard
  
  November 2025
  
  bioRxiv | November 2025
  
  DOI
- Evidence Aggregator: AI reasoning applied to rare disease diagnostics
  
  Hope Twede, Ashley Conard, Lynn Pais, Samantha Brye, Emily O’Heir, Greg Smith, Ron Paulsen, Christina A. Austin-Tse, Alex Bloemendal, Cas Simons, Scott Saponas, Miah Wander, Daniel G. MacArthur, Heidi Rehm
  
  March 2025
  
  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, 제 26 권(7): pp. 2864-2875
  
  Publication
- Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders.
  
  Hope Twede
  
  Neurology Genetics | November 2019, 제 5 권(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, 제 9 권(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, 제 11 권(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, 제 62 권(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, 제 81 권: 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, 제 17 권(12): pp. 2070
  
  DOI Publication
- Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
  
  Hope Twede
  
  BioMed Research International | November 2016, 제 2016 권: pp. 3284534-3284534
  
  DOI Publication

- The Evidence Aggregator: AI reasoning applied to rare disease diagnostics
  
  Hope Twede, Lynn Pais, S. Bryen, Emily O’Heir, Greg Smith, Ron Paulsen, C. Austin-Tse, A. Bloemendal, C. Simons, Amanda K. Hall, Scott Saponas, Jeremiah (Miah) Wander, Daniel G. MacArthur, Heidi L. Rehm, Ashley Conard
  
  November 2025
  
  bioRxiv | November 2025
  
  DOI
- Evidence Aggregator: AI reasoning applied to rare disease diagnostics
  
  Hope Twede, Ashley Conard, Lynn Pais, Samantha Brye, Emily O’Heir, Greg Smith, Ron Paulsen, Christina A. Austin-Tse, Alex Bloemendal, Cas Simons, Scott Saponas, Miah Wander, Daniel G. MacArthur, Heidi Rehm
  
  March 2025
  
  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, 제 26 권(7): pp. 2864-2875
  
  Publication
- Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders.
  
  Hope Twede
  
  Neurology Genetics | November 2019, 제 5 권(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, 제 9 권(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, 제 11 권(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, 제 62 권(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, 제 81 권: 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, 제 17 권(12): pp. 2070
  
  DOI Publication
- Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
  
  Hope Twede
  
  BioMed Research International | November 2016, 제 2016 권: pp. 3284534-3284534
  
  DOI Publication
- Evidence Aggregator: AI reasoning applied to rare disease diagnostics
  
  Hope Twede, Ashley Conard, Lynn Pais, Samantha Brye, Emily O’Heir, Greg Smith, Ron Paulsen, Christina A. Austin-Tse, Alex Bloemendal, Cas Simons, Scott Saponas, Miah Wander, Daniel G. MacArthur, Heidi Rehm
  
  March 2025
  
  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, 제 26 권(7): pp. 2864-2875
  
  Publication

- The Evidence Aggregator: AI reasoning applied to rare disease diagnostics
  
  Hope Twede, Lynn Pais, S. Bryen, Emily O’Heir, Greg Smith, Ron Paulsen, C. Austin-Tse, A. Bloemendal, C. Simons, Amanda K. Hall, Scott Saponas, Jeremiah (Miah) Wander, Daniel G. MacArthur, Heidi L. Rehm, Ashley Conard
  
  November 2025
  
  bioRxiv | November 2025
  
  DOI
- Evidence Aggregator: AI reasoning applied to rare disease diagnostics
  
  Hope Twede, Ashley Conard, Lynn Pais, Samantha Brye, Emily O’Heir, Greg Smith, Ron Paulsen, Christina A. Austin-Tse, Alex Bloemendal, Cas Simons, Scott Saponas, Miah Wander, Daniel G. MacArthur, Heidi Rehm
  
  March 2025
  
  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, 제 26 권(7): pp. 2864-2875
  
  Publication
- Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders.
  
  Hope Twede
  
  Neurology Genetics | November 2019, 제 5 권(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, 제 9 권(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, 제 11 권(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, 제 62 권(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, 제 81 권: 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, 제 17 권(12): pp. 2070
  
  DOI Publication
- Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
  
  Hope Twede
  
  BioMed Research International | November 2016, 제 2016 권: pp. 3284534-3284534
  
  DOI Publication

Hope Twede

출판물

The Evidence Aggregator: AI reasoning applied to rare disease diagnostics

Evidence Aggregator: AI reasoning applied to rare disease diagnostics

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

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

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

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

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

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

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

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

The Evidence Aggregator: AI reasoning applied to rare disease diagnostics

Evidence Aggregator: AI reasoning applied to rare disease diagnostics

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

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

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

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

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

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

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

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

Evidence Aggregator: AI reasoning applied to rare disease diagnostics

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

The Evidence Aggregator: AI reasoning applied to rare disease diagnostics

Evidence Aggregator: AI reasoning applied to rare disease diagnostics

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

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

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

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

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

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

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

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