Nicolette Chun (Chloe Reuter, Chloe M Reuter)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 38

Top Topics

Left Ventricular

Direct Oral Anticoagulants

Congenital Heart Disease

Top Venues

Circulation. Genomic and precision medicine

medRxiv : the preprint server for health sciences

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology

Journal of genetic counseling

This page only lists publications with an associated author ORCID identifier.

Publications

Sunil K Vasireddi, Tanja Zdolsek Draksler, Arianne Bouman, Joost Kummeling, Matthew T Wheeler, Nicolette Chun, Siddharth Srivastava, Jacqueline Harris, Paul Graham Fisher, Sanjiv M Narayan, Paul J Wang, Nitish Badhwar, Tjitske Kleefstra, Marco Valentin Perez
Arrhythmias including atrial fibrillation and congenital heart disease in Kleefstra syndrome: a possible epigenetic link. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 26 (1) (2024)
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, Sarah L Stenton, Susan Walker, Alicia Ljungdahl, Jenny Lord, Vijay S Ganesh, Jialan Ma, Alexandra C Martin-Geary, Gabrielle Lemire, Elston N D'Souza, Shan Dong, Jamie M Ellingford, David R Adams, Kirsten Allan, Madhura Bakshi, Erin E Baldwin, Seth I Berger, Jonathan A Bernstein, Natasha J Brown, Lindsay C Burrage, Kimberly Chapman, Alison G Compton, Chloe Alice Stutterd, Precilla D'Souza, Emmanuèle C Délot, Kerith-Rae Dias, Ellen R Elias, Carey-Anne Evans, Lisa Ewans, Kimberly M Ezell, Jamie L Fraser, Lyndon Gallacher, Casie A Genetti, Christina L Grant, Tobias Haack, Alma Kuechler, Seema R Lalani, Elsa Leitão, Anna Le Fevre, Richard J Leventer, Jan E Liebelt, Paul J Lockhart, Alan Sl Ma, Ellen F Macnamara, Taylor M Maurer, Hector R Mendez, Stephen B Montgomery, Marie-Cécile Nassogne, Serena Neumann, Melanie O'Leary, Emma Elizabeth Palmer, John Phillips, Georgia Pitsava, Ryan Pysar, Michael J Bamshad, Nicolette Chun, Nicole Revencu, Angelika Riess, Rocio Rius, Lance Rodan, Tony Roscioli, Jill Anne Rosenfeld, Rani Sachdev, Cas Simons, Sanjay M Sisodiya, Penny Snell, Laura Clair, Zornitza Stark, Tiong Yang Tan, Natalie B Tan, Suzanna El Temple, David R Thorburn, Cynthia J Tifft, Eloise Uebergang, Grace E VanNoy, Eric Vilain, David H Viskochil, Laura Wedd, Matthew T Wheeler, Susan M White, Monica Hsiung Wojcik, Lynne A Wolfe, Zoe Wolfenson, Changrui Xiao, David Zocche, John L Rubenstein, Eirene Markenscoff-Papadimitriou, Sebastian M Fica, Diana Baralle, Christel Depienne, Daniel G MacArthur, Joanna M M Howson, Stephan J Sanders, Anne H O'Donnell-Luria, Nicola Whiffin
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders. medRxiv : the preprint server for health sciences (2024)
Sophie Hespe, Amber Waddell, Babken Asatryan, Emma Owens, Courtney L Thaxton, Mhy-Lanie Adduru, Kailyn Anderson, Emily E Brown, Lily Hoffman-Andrews, Elizabeth S Jordan, Katherine S Josephs, Megan Mayers, Stacey Peters, Fergus Stafford, Richard Douglas Bagnall, Lucas Bronicki, Bert Callewaert, C Anwar A Chahal, Cynthia A James, Olga Jarinova, Andrew P Landstrom, Elizabeth M McNally, Brittney Murray, Laura Muiño Mosquera, Victoria N Parikh, Nicolette Chun, Roddy Walsh, Bess Wayburn, James Simon Ware, Jodie Ingles
ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy. medRxiv : the preprint server for health sciences (2024)
Sunil K Vasireddi, Tanja Zdolsek Draksler, Arianne Bouman, Joost Kummeling, Matthew T Wheeler, Nicolette Chun, Siddharth Srivastava, Jacqueline Harris, Paul Graham Fisher, Sanjiv M Narayan, Paul J Wang, Nitish Badhwar, Tjitske Kleefstra, Marco Valentin Perez
Arrhythmias including atrial fibrillation and congenital heart disease in Kleefstra syndrome: a possible epigenetic link. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 26 (1) (2024)
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, Sarah L Stenton, Susan Walker, Alicia Ljungdahl, Jenny Lord, Vijay S Ganesh, Jialan Ma, Alexandra C Martin-Geary, Gabrielle Lemire, Elston N D'Souza, Shan Dong, Jamie M Ellingford, David R Adams, Kirsten Allan, Madhura Bakshi, Erin E Baldwin, Seth I Berger, Jonathan A Bernstein, Natasha J Brown, Lindsay C Burrage, Kimberly Chapman, Alison G Compton, Chloe Alice Stutterd, Precilla D'Souza, Emmanuèle C Délot, Kerith-Rae Dias, Ellen R Elias, Carey-Anne Evans, Lisa Ewans, Kimberly M Ezell, Jamie L Fraser, Lyndon Gallacher, Casie A Genetti, Christina L Grant, Tobias Haack, Alma Kuechler, Seema R Lalani, Elsa Leitão, Anna Le Fevre, Richard J Leventer, Jan E Liebelt, Paul J Lockhart, Alan Sl Ma, Ellen F Macnamara, Taylor M Maurer, Hector R Mendez, Stephen B Montgomery, Marie-Cécile Nassogne, Serena Neumann, Melanie O'Leary, Emma Elizabeth Palmer, John Phillips, Georgia Pitsava, Ryan Pysar, Michael J Bamshad, Nicolette Chun, Nicole Revencu, Angelika Riess, Rocio Rius, Lance Rodan, Tony Roscioli, Jill Anne Rosenfeld, Rani Sachdev, Cas Simons, Sanjay M Sisodiya, Penny Snell, Laura Clair, Zornitza Stark, Tiong Yang Tan, Natalie B Tan, Suzanna El Temple, David R Thorburn, Cynthia J Tifft, Eloise Uebergang, Grace E VanNoy, Eric Vilain, David H Viskochil, Laura Wedd, Matthew T Wheeler, Susan M White, Monica Hsiung Wojcik, Lynne A Wolfe, Zoe Wolfenson, Changrui Xiao, David Zocche, John L Rubenstein, Eirene Markenscoff-Papadimitriou, Sebastian M Fica, Diana Baralle, Christel Depienne, Daniel G MacArthur, Joanna M M Howson, Stephan J Sanders, Anne H O'Donnell-Luria, Nicola Whiffin
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders. medRxiv : the preprint server for health sciences (2024)
Vikki A Krysov, Rachel H Wilson, Nicholas S Ten, Nathan Youlton, Hannah N De Jong, Shirley Sutton, Yong Huang, Nicolette Chun, Megan E Grove, Matthew T Wheeler, Euan A Ashley, Victoria N Parikh
Regional Variation in Cardiovascular Genes Enables a Tractable Genome Editing Strategy. Circulation. Genomic and precision medicine 17 (2) (2024)
Vikki A Krysov, Rachel H Wilson, Nicholas S Ten, Nathan Youlton, Hannah N De Jong, Shirley Sutton, Yong Huang, Nicolette Chun, Megan E Grove, Matthew T Wheeler, Euan A Ashley, Victoria N Parikh
Regional Variation in Cardiovascular Genes Enables a Tractable Genome Editing Strategy. Circulation. Genomic and precision medicine 17 (2) (2024)
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, Sarah L Stenton, Susan Walker, Alicia Ljungdahl, Jenny Lord, Vijay S Ganesh, Jialan Ma, Alexandra C Martin-Geary, Gabrielle Lemire, Elston N D'Souza, Shan Dong, Jamie M Ellingford, David R Adams, Kirsten Allan, Madhura Bakshi, Erin E Baldwin, Seth I Berger, Jonathan A Bernstein, Natasha J Brown, Lindsay C Burrage, Kimberly Chapman, Alison G Compton, Chloe Alice Stutterd, Precilla D'Souza, Emmanuèle C Délot, Kerith-Rae Dias, Ellen R Elias, Carey-Anne Evans, Lisa Ewans, Kimberly M Ezell, Jamie L Fraser, Lyndon Gallacher, Casie A Genetti, Christina L Grant, Tobias Haack, Alma Kuechler, Seema R Lalani, Elsa Leitão, Anna Le Fevre, Richard J Leventer, Jan E Liebelt, Paul J Lockhart, Alan Sl Ma, Ellen F Macnamara, Taylor M Maurer, Hector R Mendez, Stephen B Montgomery, Marie-Cécile Nassogne, Serena Neumann, Melanie O'Leary, Emma Elizabeth Palmer, John Phillips, Georgia Pitsava, Ryan Pysar, Michael J Bamshad, Nicolette Chun, Nicole Revencu, Angelika Riess, Rocio Rius, Lance Rodan, Tony Roscioli, Jill Anne Rosenfeld, Rani Sachdev, Cas Simons, Sanjay M Sisodiya, Penny Snell, Laura St Clair, Zornitza Stark, Tiong Yang Tan, Natalie B Tan, Suzanna El Temple, David R Thorburn, Cynthia J Tifft, Eloise Uebergang, Grace E VanNoy, Eric Vilain, David H Viskochil, Laura Wedd, Matthew T Wheeler, Susan M White, Monica Hsiung Wojcik, Lynne A Wolfe, Zoe Wolfenson, Changrui Xiao, David Zocche, John L Rubenstein, Eirene Markenscoff-Papadimitriou, Sebastian M Fica, Diana Baralle, Christel Depienne, Daniel G MacArthur, Joanna M M Howson, Stephan J Sanders, Anne H O'Donnell-Luria, Nicola Whiffin
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders. medRxiv : the preprint server for health sciences (2024)
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, Sarah L Stenton, Susan Walker, Alicia Ljungdahl, Jenny Lord, Vijay S Ganesh, Jialan Ma, Alexandra C Martin-Geary, Gabrielle Lemire, Elston N D'Souza, Shan Dong, Jamie M Ellingford, David R Adams, Kirsten Allan, Madhura Bakshi, Erin E Baldwin, Seth I Berger, Jonathan A Bernstein, Natasha J Brown, Lindsay C Burrage, Kimberly Chapman, Alison G Compton, Chloe Alice Stutterd, Precilla D'Souza, Emmanuèle C Délot, Kerith-Rae Dias, Ellen R Elias, Carey-Anne Evans, Lisa Ewans, Kimberly M Ezell, Jamie L Fraser, Lyndon Gallacher, Casie A Genetti, Christina L Grant, Tobias Haack, Alma Kuechler, Seema R Lalani, Elsa Leitão, Anna Le Fevre, Richard J Leventer, Jan E Liebelt, Paul J Lockhart, Alan Sl Ma, Ellen F Macnamara, Taylor M Maurer, Hector R Mendez, Stephen B Montgomery, Marie-Cécile Nassogne, Serena Neumann, Melanie O'Leary, Emma Elizabeth Palmer, John Phillips, Georgia Pitsava, Ryan Pysar, Michael J Bamshad, Nicolette Chun, Nicole Revencu, Angelika Riess, Rocio Rius, Lance Rodan, Tony Roscioli, Jill Anne Rosenfeld, Rani Sachdev, Cas Simons, Sanjay M Sisodiya, Penny Snell, Laura Clair, Zornitza Stark, Tiong Yang Tan, Natalie B Tan, Suzanna El Temple, David R Thorburn, Cynthia J Tifft, Eloise Uebergang, Grace E VanNoy, Eric Vilain, David H Viskochil, Laura Wedd, Matthew T Wheeler, Susan M White, Monica Hsiung Wojcik, Lynne A Wolfe, Zoe Wolfenson, Changrui Xiao, David Zocche, John L Rubenstein, Eirene Markenscoff-Papadimitriou, Sebastian M Fica, Diana Baralle, Christel Depienne, Daniel G MacArthur, Joanna M M Howson, Stephan J Sanders, Anne H O'Donnell-Luria, Nicola Whiffin
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders. medRxiv : the preprint server for health sciences (2024)
Sophie Hespe, Amber Waddell, Babken Asatryan, Emma Owens, Courtney L Thaxton, Mhy-Lanie Adduru, Kailyn Anderson, Emily Brown, Lily Hoffman-Andrews, Elizabeth S Jordan, Katherine S Josephs, Megan Mayers, Stacey Peters, Fergus Stafford, Richard Douglas Bagnall, Lucas Bronicki, Bert Callewaert, C Anwar Chahal, Cynthia A James, Olga Jarinova, Andrew P Landstrom, Elizabeth M McNally, Brittney Murray, Laura Muiño Mosquera, Victoria N Parikh, Nicolette Chun, Roddy Walsh, Bess Wayburn, James Simon Ware, Jodie Ingles
ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy. medRxiv : the preprint server for health sciences (2024)
Sunil K Vasireddi, Tanja Zdolsek Draksler, Arianne Bouman, Joost Kummeling, Matthew T Wheeler, Nicolette Chun, Siddharth Srivastava, Jacqueline Harris, Paul Graham Fisher, Sanjiv M Narayan, Paul J Wang, Nitish Badhwar, Tjitske Kleefstra, Marco Valentin Perez
Arrhythmias including Atrial Fibrillation and Congenital Heart Disease in Kleefstra Syndrome: a possible epigenetic link. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology (2024)
Sophie Hespe, Amber Waddell, Babken Asatryan, Emma Owens, Courtney L Thaxton, Mhy-Lanie Adduru, Kailyn Anderson, Emily Brown, Lily Hoffman-Andrews, Elizabeth S Jordan, Katherine S Josephs, Megan Mayers, Stacey Peters, Fergus Stafford, Richard Douglas Bagnall, Lucas Bronicki, Bert Callewaert, C Anwar Chahal, Cynthia A James, Olga Jarinova, Andrew P Landstrom, Elizabeth M McNally, Brittney Murray, Laura Muiño Mosquera, Victoria N Parikh, Nicolette Chun, Roddy Walsh, Bess Wayburn, James Simon Ware, Jodie Ingles
ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy. medRxiv : the preprint server for health sciences (2024)
Vikki A Krysov, Rachel H Wilson, Nicholas S Ten, Nathan Youlton, Hannah N De Jong, Shirley Sutton, Yong Huang, Nicolette Chun, Megan E Grove, Matthew T Wheeler, Euan A Ashley, Victoria N Parikh
Regional Variation in Cardiovascular Genes Enables a Tractable Genome Editing Strategy. Circulation. Genomic and precision medicine (2024)
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, Sarah L Stenton, Susan Walker, Alicia Ljungdahl, Jenny Lord, Vijay S Ganesh, Jialan Ma, Alexandra C Martin-Geary, Gabrielle Lemire, Elston N D'Souza, Shan Dong, Jamie M Ellingford, David R Adams, Kirsten Allan, Madhura Bakshi, Erin E Baldwin, Seth I Berger, Jonathan A Bernstein, Natasha J Brown, Lindsay C Burrage, Kimberly Chapman, Alison G Compton, Chloe Alice Stutterd, Precilla D'Souza, Emmanuèle C Délot, Kerith-Rae Dias, Ellen R Elias, Carey-Anne Evans, Lisa Ewans, Kimberly M Ezell, Jamie L Fraser, Lyndon Gallacher, Casie A Genetti, Christina L Grant, Tobias Haack, Alma Kuechler, Seema R Lalani, Elsa Leitão, Anna Le Fevre, Richard J Leventer, Jan E Liebelt, Paul J Lockhart, Alan Sl Ma, Ellen F Macnamara, Taylor M Maurer, Hector R Mendez, Stephen B Montgomery, Marie-Cécile Nassogne, Serena Neumann, Melanie O'Leary, Emma Elizabeth Palmer, John Phillips, Georgia Pitsava, Ryan Pysar, Michael J Bamshad, Nicolette Chun, Nicole Revencu, Angelika Riess, Rocio Rius, Lance Rodan, Tony Roscioli, Jill Anne Rosenfeld, Rani Sachdev, Cas Simons, Sanjay M Sisodiya, Penny Snell, Laura Clair, Zornitza Stark, Tiong Yang Tan, Natalie B Tan, Suzanna El Temple, David R Thorburn, Cynthia J Tifft, Eloise Uebergang, Grace E VanNoy, Eric Vilain, David H Viskochil, Laura Wedd, Matthew T Wheeler, Susan M White, Monica Hsiung Wojcik, Lynne A Wolfe, Zoe Wolfenson, Changrui Xiao, David Zocche, John L Rubenstein, Eirene Markenscoff-Papadimitriou, Sebastian M Fica, Diana Baralle, Christel Depienne, Daniel G MacArthur, Joanna M M Howson, Stephan J Sanders, Anne H O'Donnell-Luria, Nicola Whiffin
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders. medRxiv : the preprint server for health sciences (2024)
Michelle Frees, Jennefer N Carter, Matthew T Wheeler, Nicolette Chun
The current landscape of clinical exome and genome reanalysis in the U.S. Journal of genetic counseling (2024)
Sunil K Vasireddi, Tanja Zdolsek Draksler, Arianne Bouman, Joost Kummeling, Matthew T Wheeler, Nicolette Chun, Siddharth Srivastava, Jacqueline Harris, Paul Graham Fisher, Sanjiv M Narayan, Paul J Wang, Nitish Badhwar, Tjitske Kleefstra, Marco Valentin Perez
Arrhythmias including atrial fibrillation and congenital heart disease in Kleefstra syndrome: a possible epigenetic link. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 26 (1) (2024)
Sunil K Vasireddi, Tanja Zdolsek Draksler, Arianne Bouman, Joost Kummeling, Matthew T Wheeler, Nicolette Chun, Siddharth Srivastava, Jacqueline Harris, Paul Graham Fisher, Sanjiv M Narayan, Paul J Wang, Nitish Badhwar, Tjitske Kleefstra, Marco Valentin Perez
Arrhythmias including atrial fibrillation and congenital heart disease in Kleefstra syndrome: a possible epigenetic link. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 26 (1) (2024)
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, Sarah L Stenton, Susan Walker, Alicia Ljungdahl, Jenny Lord, Vijay S Ganesh, Jialan Ma, Alexandra C Martin-Geary, Gabrielle Lemire, Elston N D'Souza, Shan Dong, Jamie M Ellingford, David R Adams, Kirsten Allan, Madhura Bakshi, Erin E Baldwin, Seth I Berger, Jonathan A Bernstein, Natasha J Brown, Lindsay C Burrage, Kimberly Chapman, Alison G Compton, Chloe Alice Stutterd, Precilla D'Souza, Emmanuèle C Délot, Kerith-Rae Dias, Ellen R Elias, Carey-Anne Evans, Lisa Ewans, Kimberly M Ezell, Jamie L Fraser, Lyndon Gallacher, Casie A Genetti, Christina L Grant, Tobias Haack, Alma Kuechler, Seema R Lalani, Elsa Leitão, Anna Le Fevre, Richard J Leventer, Jan E Liebelt, Paul J Lockhart, Alan Sl Ma, Ellen F Macnamara, Taylor M Maurer, Hector R Mendez, Stephen B Montgomery, Marie-Cécile Nassogne, Serena Neumann, Melanie O'Leary, Emma Elizabeth Palmer, John Phillips, Georgia Pitsava, Ryan Pysar, Michael J Bamshad, Nicolette Chun, Nicole Revencu, Angelika Riess, Rocio Rius, Lance Rodan, Tony Roscioli, Jill Anne Rosenfeld, Rani Sachdev, Cas Simons, Sanjay M Sisodiya, Penny Snell, Laura Clair, Zornitza Stark, Tiong Yang Tan, Natalie B Tan, Suzanna El Temple, David R Thorburn, Cynthia J Tifft, Eloise Uebergang, Grace E VanNoy, Eric Vilain, David H Viskochil, Laura Wedd, Matthew T Wheeler, Susan M White, Monica Hsiung Wojcik, Lynne A Wolfe, Zoe Wolfenson, Changrui Xiao, David Zocche, John L Rubenstein, Eirene Markenscoff-Papadimitriou, Sebastian M Fica, Diana Baralle, Christel Depienne, Daniel G MacArthur, Joanna M M Howson, Stephan J Sanders, Anne H O'Donnell-Luria, Nicola Whiffin
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders. medRxiv : the preprint server for health sciences (2024)
Sunil K Vasireddi, Tanja Zdolsek Draksler, Arianne Bouman, Joost Kummeling, Matthew T Wheeler, Nicolette Chun, Siddharth Srivastava, Jacqueline Harris, Paul Graham Fisher, Sanjiv M Narayan, Paul J Wang, Nitish Badhwar, Tjitske Kleefstra, Marco Valentin Perez
Arrhythmias including atrial fibrillation and congenital heart disease in Kleefstra syndrome: a possible epigenetic link. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 26 (1) (2024)
Brendan J Floyd, Jochen Weile, Prince J Kannankeril, Andrew M Glazer, Nicolette Chun, Calum A MacRae, Euan A Ashley, Dan M Roden, Frederick P Roth, Victoria N Parikh
Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest. Circulation. Genomic and precision medicine 16 (1) (2023)
Brendan J Floyd, Jochen Weile, Prince J Kannankeril, Andrew M Glazer, Nicolette Chun, Calum A MacRae, Euan A Ashley, Dan M Roden, Frederick P Roth, Victoria N Parikh
Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest. Circulation. Genomic and precision medicine 16 (1) (2023)
Brendan J Floyd, Jochen Weile, Prince J Kannankeril, Andrew M Glazer, Nicolette Chun, Calum A MacRae, Euan A Ashley, Dan M Roden, Frederick P Roth, Victoria N Parikh
Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest. Circulation. Genomic and precision medicine 16 (1) (2023)
Brendan J Floyd, Jochen Weile, Prince J Kannankeril, Andrew M Glazer, Nicolette Chun, Calum A MacRae, Euan A Ashley, Dan M Roden, Frederick P Roth, Victoria N Parikh
Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest. Circulation. Genomic and precision medicine (2023)
Brendan J Floyd, Jochen Weile, Prince J Kannankeril, Andrew M Glazer, Nicolette Chun, Calum A MacRae, Euan A Ashley, Dan M Roden, Frederick P Roth, Victoria N Parikh
Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest. Circulation. Genomic and precision medicine 16 (1) (2023)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
Tiffany T Nguyen Dolphyn, Kelly E Ormond, Scott M Weissman, Helen J Kim, Nicolette Chun
Patient experiences with clinical confirmatory genetic testing after using direct-to-consumer raw DNA and third-party genetic interpretation services. Translational behavioral medicine (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
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Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
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Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine (2022)
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Diane B Zastrow, Jennefer N Carter, Devon E Bonner, Nicolette Chun, Liliana Fernandez, Megan E Grove, Dianna G Fisk, null null, Yaping Yang, Christine M Eng, Patricia A Ward, David Bick, Elizabeth A Worthey, Paul Graham Fisher, Euan A Ashley, Jonathan A Bernstein, Matthew T Wheeler
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Chloe Reuter, Nicolette Chun, Mitchel Pariani, Andrea Hanson-Kahn
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