Michel C Tchan (Michel Tchan)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 18

Top Topics

Hypertrophic Cardiomyopathy

Low Birth Weight

Obstructive Sleep Apnea

Advance Care Planning

Top Venues

Clinical journal of the American Society of Nephrology : CJASN

Neurology. Genetics

Internal medicine journal

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

Publications

Kathleen M Nicholls, Charles Denaro, Michel C Tchan, Carolyn Jane Ellaway, Drago Bratkovic, Sheridan Campbell, Megan Fookes, Mark Thomas
Fabry-specific treatment in Australia: time to align eligibility criteria with international best practices. Internal medicine journal (2024)
Amali C Mallawaarachchi, Lindsay Fowles, Louise Wardrop, Alasdair Wood, Rosie O'Shea, Erik Biros, Trudie Harris, Stephen I Alexander, Simon D Bodek, Neil Boudville, Jo Burke, Leslie Burnett, Sarah Casauria, Steve Chadban, Aron Chakera, Sam Crafter, Pei Dai, Paul De Fazio, Randall Faull, Andrew Honda, Vanessa Huntley, Sadia Jahan, Kushani Jayasinghe, Matthew D Jose, Anna Leaver, Mandi MacShane, Evanthia Olympia Madelli, Kathleen M Nicholls, Rhonda Pawlowski, Gopala K Rangan, Paul Snelling, Jacqueline Soraru, Madhivanan Sundaram, Michel C Tchan, Giulia M Valente, Mathew J Wallis, Laura Wedd, Matthew Welland, John B Whitlam, Ella J Wilkins, Hugh McCarthy, Cas Simons, Catherine Quinlan, Chirag Patel, Zornitza Stark, Andrew John Mallett
Genomic Testing in Patients with Kidney Failure of an Unknown Cause: A National Australian Study. Clinical journal of the American Society of Nephrology : CJASN 19 (7) (2024)
Amali C Mallawaarachchi, Lindsay Fowles, Louise Wardrop, Alasdair Wood, Rosie O'Shea, Erik Biros, Trudie Harris, Stephen I Alexander, Simon D Bodek, Neil Boudville, Jo Burke, Leslie Burnett, Sarah Casauria, Steve Chadban, Aron Chakera, Sam Crafter, Pei Dai, Paul De Fazio, Randall Faull, Andrew Honda, Vanessa Huntley, Sadia Jahan, Kushani Jayasinghe, Matthew D Jose, Anna Leaver, Mandi MacShane, Evanthia Olympia Madelli, Kathleen M Nicholls, Rhonda Pawlowski, Gopala K Rangan, Paul Snelling, Jacqueline Soraru, Madhivanan Sundaram, Michel C Tchan, Giulia M Valente, Mathew J Wallis, Laura Wedd, Matthew Welland, John B Whitlam, Ella J Wilkins, Hugh McCarthy, Cas Simons, Catherine Quinlan, Chirag Patel, Zornitza Stark, Andrew John Mallett
Genomic Testing in Patients with Kidney Failure of an Unknown Cause: a National Australian Study. Clinical journal of the American Society of Nephrology : CJASN (2024)
Amali C Mallawaarachchi, Lindsay Fowles, Louise Wardrop, Alasdair Wood, Rosie O'Shea, Erik Biros, Trudie Harris, Stephen I Alexander, Simon D Bodek, Neil Boudville, Jo Burke, Leslie Burnett, Sarah Casauria, Steve Chadban, Aron Chakera, Sam Crafter, Pei Dai, Paul De Fazio, Randall Faull, Andrew Honda, Vanessa Huntley, Sadia Jahan, Kushani Jayasinghe, Matthew D Jose, Anna Leaver, Mandi MacShane, Evanthia Olympia Madelli, Kathleen M Nicholls, Rhonda Pawlowski, Gopala K Rangan, Paul Snelling, Jacqueline Soraru, Madhivanan Sundaram, Michel C Tchan, Giulia M Valente, Mathew J Wallis, Laura Wedd, Matthew Welland, John B Whitlam, Ella J Wilkins, Hugh McCarthy, Cas Simons, Catherine Quinlan, Chirag Patel, Zornitza Stark, Andrew John Mallett
Genomic Testing in Patients with Kidney Failure of an Unknown Cause: A National Australian Study. Clinical journal of the American Society of Nephrology : CJASN 19 (7) (2024)
Amali C Mallawaarachchi, Lindsay Fowles, Louise Wardrop, Alasdair Wood, Rosie O'Shea, Erik Biros, Trudie Harris, Stephen I Alexander, Simon D Bodek, Neil Boudville, Jo Burke, Leslie Burnett, Sarah Casauria, Steve Chadban, Aron Chakera, Sam Crafter, Pei Dai, Paul De Fazio, Randall Faull, Andrew Honda, Vanessa Huntley, Sadia Jahan, Kushani Jayasinghe, Matthew D Jose, Anna Leaver, Mandi MacShane, Evanthia Olympia Madelli, Kathleen M Nicholls, Rhonda Pawlowski, Gopala K Rangan, Paul Snelling, Jacqueline Soraru, Madhivanan Sundaram, Michel C Tchan, Giulia M Valente, Mathew J Wallis, Laura Wedd, Matthew Welland, John B Whitlam, Ella J Wilkins, Hugh McCarthy, Cas Simons, Catherine Quinlan, Chirag Patel, Zornitza Stark, Andrew John Mallett
Genomic Testing in Patients with Kidney Failure of an Unknown Cause: A National Australian Study. Clinical journal of the American Society of Nephrology : CJASN 19 (7) (2024)
Amali C Mallawaarachchi, Lindsay Fowles, Louise Wardrop, Alasdair Wood, Rosie O'Shea, Erik Biros, Trudie Harris, Stephen I Alexander, Simon D Bodek, Neil Boudville, Jo Burke, Leslie Burnett, Sarah Casauria, Steve Chadban, Aron Chakera, Sam Crafter, Pei Dai, Paul De Fazio, Randall Faull, Andrew Honda, Vanessa Huntley, Sadia Jahan, Kushani Jayasinghe, Matthew D Jose, Anna Leaver, Mandi MacShane, Evanthia Olympia Madelli, Kathleen M Nicholls, Rhonda Pawlowski, Gopala K Rangan, Paul Snelling, Jacqueline Soraru, Madhivanan Sundaram, Michel C Tchan, Giulia M Valente, Mathew J Wallis, Laura Wedd, Matthew Welland, John B Whitlam, Ella J Wilkins, Hugh McCarthy, Cas Simons, Catherine Quinlan, Chirag Patel, Zornitza Stark, Andrew John Mallett
Genomic Testing in Patients with Kidney Failure of an Unknown Cause: A National Australian Study. Clinical journal of the American Society of Nephrology : CJASN 19 (7) (2024)
Kathleen M Nicholls, Charles Denaro, Michel C Tchan, Carolyn Jane Ellaway, Drago Bratkovic, Sheridan Campbell, Megan Fookes, Mark Thomas
Fabry-specific treatment in Australia: time to align eligibility criteria with international best practices. Internal medicine journal 54 (6) (2024)
Susan Thompson, Ashley Hertzog, Arthavan Selvanathan, Kiera Batten, Katherine Lewis, Janelle Nisbet, Ashleigh Mitchell, Troy Dalkeith, Kate Billmore, Francesca Moore, Adviye Ayper Tolun, Beena Devanapalli, Drago Bratkovic, Cathie Hilditch, Yusof Rahman, Michel C Tchan, Kaustuv Bhattacharya
Treatment of HMG-CoA Lyase Deficiency-Longitudinal Data on Clinical and Nutritional Management of 10 Australian Cases. Nutrients 15 (3) (2023)
Sean Massey, Yiran Guo, Lisa G Riley, Nicole J Van Bergen, Sarah A Sandaradura, Elizabeth McCusker, Michel C Tchan, Christel Thauvin-Robinet, Quentin Thomas, Thibault Moreau, Mark Davis, Daphne Smits, Grazia M S Mancini, Hakon Hakonarson, Sandra Cooper, John Chrisodoulou
Expanding the Allelic Heterogeneity of ANO10 -Associated Autosomal Recessive Cerebellar Ataxia. Neurology. Genetics 9 (1) (2023)
Sean Massey, Yiran Guo, Lisa G Riley, Nicole J Van Bergen, Sarah A Sandaradura, Elizabeth McCusker, Michel C Tchan, Christel Thauvin-Robinet, Quentin Thomas, Thibault Moreau, Mark Davis, Daphne Smits, Grazia M S Mancini, Hakon Hakonarson, Sandra Cooper, John Chrisodoulou
Expanding the Allelic Heterogeneity of ANO10 -Associated Autosomal Recessive Cerebellar Ataxia. Neurology. Genetics 9 (1) (2023)
Susan Thompson, Ashley Hertzog, Arthavan Selvanathan, Kiera Batten, Katherine Lewis, Janelle Nisbet, Ashleigh Mitchell, Troy Dalkeith, Kate Billmore, Francesca Moore, Adviye Ayper Tolun, Beena Devanapalli, Drago Bratkovic, Cathie Hilditch, Yusof Rahman, Michel C Tchan, Kaustuv Bhattacharya
Treatment of HMG-CoA Lyase Deficiency-Longitudinal Data on Clinical and Nutritional Management of 10 Australian Cases. Nutrients 15 (3) (2023)
Susan Thompson, Ashley Hertzog, Arthavan Selvanathan, Kiera Batten, Katherine Lewis, Janelle Nisbet, Ashleigh Mitchell, Troy Dalkeith, Kate Billmore, Francesca Moore, Adviye Ayper Tolun, Beena Devanapalli, Drago Bratkovic, Cathie Hilditch, Yusof Rahman, Michel C Tchan, Kaustuv Bhattacharya
Treatment of HMG-CoA Lyase Deficiency-Longitudinal Data on Clinical and Nutritional Management of 10 Australian Cases. Nutrients 15 (3) (2023)
Demi Beneru, Michel C Tchan, Kate Billmore, Roshini Nayyar
Glycogen storage disease type IIIa in pregnant women: A guide to management. JIMD reports 63 (3) (2022)
Matthew Zada, Queenie Lo, Siddharth J Trivedi, Mehmet Harapoz, Anita C Boyd, Kerry Devine, Norman Sadick, Michel C Tchan, Liza Thomas
Electrocardiographic Characteristics and Their Correlation with Echocardiographic Alterations in Fabry Disease. Journal of cardiovascular development and disease 9 (1) (2022)
Igor Stevanovski, Sanjog R Chintalaphani, Hasindu Gamaarachchi, James M Ferguson, Sandy S Pineda, Carolin K Scriba, Michel C Tchan, Victor S C Fung, Karl Ng, Andrea Cortese, Henry Houlden, Carol Dobson-Stone, Lauren Fitzpatrick, Glenda M Halliday, Gianina Ravenscroft, Mark R Davis, Nigel G Laing, Avi Fellner, Marina L Kennerson, Kishore Raj Kumar, Ira W Deveson
Comprehensive genetic diagnosis of tandem repeat expansion disorders with programmable targeted nanopore sequencing. Science advances 8 (9) (2022)
Brianna L Kline, Sylvie Jaillard, Katrina M Bell, Shabnam Bakhshalizadeh, Gorjana Robevska, Jocelyn van den Bergen, Jérôme Dulon, Katie L Ayers, John Chrisodoulou, Michel C Tchan, Philippe Touraine, Andrew H Sinclair, Elena Jane Tucker
Integral Role of the Mitochondrial Ribosome in Supporting Ovarian Function: MRPS7 Variants in Syndromic Premature Ovarian Insufficiency. Genes 13 (11) (2022)
Leigh B Waddell, Samantha J Bryen, Beryl B Cummings, Adam M Bournazos, Frances J Evesson, Himanshu Joshi, Jamie L Marshall, Taru Tukiainen, Elise Valkanas, Ben Weisburd, Simon Sadedin, Mark R Davis, Fathimath Faiz, Rebecca Gooding, Sarah A Sandaradura, Gina L O'Grady, Michel C Tchan, David R Mowat, Emily C Oates, Michelle A Farrar, Hugo Sampaio, Alan Sl Ma, Katherine Neas, Min-Xia Wang, Amanda Charlton, Charles Chan, Diane N Kenwright, Nicole Graf, Susan Arbuckle, Nigel F Clarke, Daniel G MacArthur, Kristi J Jones, Monkol Lek, Sandra T Cooper
WGS and RNA Studies Diagnose Noncoding DMD Variants in Males With High Creatine Kinase. Neurology. Genetics 7 (1) (2021)
Michel C Tchan
Hyperammonemia and lactic acidosis in adults: Differential diagnoses with a focus on inborn errors of metabolism. Reviews in endocrine & metabolic disorders 19 (1) (2019)