Gareth S Baynam (Gareth Baynam)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 27

Top Venues

Nature genetics

Nature communications

Orphanet journal of rare diseases

Nature

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

Publications

Gareth S Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R McMaster, Elissa Prichep, Étienne Richer, Francois Hendrikus van der Westhuizen, Gabriela M Repetto, Helen Louise Malherbe, Juergen K V Reichardt, Laura Arbour, Maui Hudson, Kelly du Plessis, Melissa A Haendel, Phillip Wilcox, Sally Ann Lynch, Shamir Rind, Simon Easteal, Xavier Estivil, Nadine Caron, Meck Chongo, Yarlalu Thomas, Mary Catherine V Letinturier, Barend Christiaan Vorster
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature genetics 56 (2) (2024)
Rudrarup Bhattacharjee, Lachlan A Jolly, Mark A Corbett, Ing Chee Wee, Sushma R Rao, Alison E Gardner, Tarin Ritchie, Eline J H van Hugte, Ummi Ciptasari, Sandra G Piltz, Jacqueline E Noll, Nazzmer Nazri, Clare L van Eyk, Melissa White, Dani Fornarino, Cathryn Poulton, Gareth S Baynam, Lyndsey E Collins-Praino, Marten F Snel, Nael Nadif Kasri, Kim M Hemsley, Paul Q Thomas, Raman Kumar, Jozef Gecz
Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment. Nature communications 15 (1) (2024)
Gareth S Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R McMaster, Elissa Prichep, Étienne Richer, Francois Hendrikus van der Westhuizen, Gabriela M Repetto, Helen Louise Malherbe, Juergen K V Reichardt, Laura Arbour, Maui Hudson, Kelly du Plessis, Melissa A Haendel, Phillip Wilcox, Sally Ann Lynch, Shamir Rind, Simon Easteal, Xavier Estivil, Nadine Caron, Meck Chongo, Yarlalu Thomas, Mary Catherine V Letinturier, Barend Christiaan Vorster
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature genetics 56 (2) (2024)
Rudrarup Bhattacharjee, Lachlan A Jolly, Mark A Corbett, Ing Chee Wee, Sushma R Rao, Alison E Gardner, Tarin Ritchie, Eline J H van Hugte, Ummi Ciptasari, Sandra G Piltz, Jacqueline E Noll, Nazzmer Nazri, Clare L van Eyk, Melissa White, Dani Fornarino, Cathryn Poulton, Gareth S Baynam, Lyndsey E Collins-Praino, Marten F Snel, Nael Nadif Kasri, Kim M Hemsley, Paul Q Thomas, Raman Kumar, Jozef Gecz
Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment. Nature communications 15 (1) (2024)
Rudrarup Bhattacharjee, Lachlan A Jolly, Mark A Corbett, Ing Chee Wee, Sushma R Rao, Alison E Gardner, Tarin Ritchie, Eline J H van Hugte, Ummi Ciptasari, Sandra G Piltz, Jacqueline E Noll, Nazzmer Nazri, Clare L van Eyk, Melissa White, Dani Fornarino, Cathryn Poulton, Gareth S Baynam, Lyndsey E Collins-Praino, Marten F Snel, Nael Nadif Kasri, Kim M Hemsley, Paul Q Thomas, Raman Kumar, Jozef Gecz
Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment. Nature communications 15 (1) (2024)
Gareth S Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R McMaster, Elissa Prichep, Étienne Richer, Francois Hendrikus van der Westhuizen, Gabriela M Repetto, Helen Louise Malherbe, Juergen K V Reichardt, Laura Arbour, Maui Hudson, Kelly du Plessis, Melissa A Haendel, Phillip Wilcox, Sally Ann Lynch, Shamir Rind, Simon Easteal, Xavier Estivil, Nadine Caron, Meck Chongo, Yarlalu Thomas, Mary Catherine V Letinturier, Barend Christiaan Vorster
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature genetics 56 (2) (2024)
Gareth S Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R McMaster, Elissa Prichep, Étienne Richer, Francois Hendrikus van der Westhuizen, Gabriela M Repetto, Helen Louise Malherbe, Juergen K V Reichardt, Laura Arbour, Maui Hudson, Kelly du Plessis, Melissa A Haendel, Phillip Wilcox, Sally Ann Lynch, Shamir Rind, Simon Easteal, Xavier Estivil, Nadine Caron, Meck Chongo, Yarlalu Thomas, Mary Catherine V Letinturier, Barend Christiaan Vorster
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature genetics 56 (2) (2024)
Gareth S Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R McMaster, Elissa Prichep, Étienne Richer, Francois Hendrikus van der Westhuizen, Gabriela M Repetto, Helen Louise Malherbe, Juergen K V Reichardt, Laura Arbour, Maui Hudson, Kelly du Plessis, Melissa A Haendel, Phillip Wilcox, Sally Ann Lynch, Shamir Rind, Simon Easteal, Xavier Estivil, Nadine Caron, Meck Chongo, Yarlalu Thomas, Mary Catherine V Letinturier, Barend Christiaan Vorster
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature genetics 56 (2) (2024)
Rudrarup Bhattacharjee, Lachlan A Jolly, Mark A Corbett, Ing Chee Wee, Sushma R Rao, Alison E Gardner, Tarin Ritchie, Eline J H van Hugte, Ummi Ciptasari, Sandra G Piltz, Jacqueline E Noll, Nazzmer Nazri, Clare L van Eyk, Melissa White, Dani Fornarino, Cathryn Poulton, Gareth S Baynam, Lyndsey E Collins-Praino, Marten F Snel, Nael Nadif Kasri, Kim M Hemsley, Paul Q Thomas, Raman Kumar, Jozef Gecz
Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment. Nature communications 15 (1) (2024)
Erin A Kelty, Michele Hansen, Sean M Randall, Dylan Gration, Gareth S Baynam, David Brian Preen
Use of privacy-preserving record linkage to examine the dispensing of pharmaceutical benefits scheme medicines to pregnant women in Western Australia. Pharmacoepidemiology and drug safety 33 (6) (2024)
Gareth S Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R McMaster, Elissa Prichep, Étienne Richer, Francois Hendrikus van der Westhuizen, Gabriela M Repetto, Helen Louise Malherbe, Juergen K V Reichardt, Laura Arbour, Maui Hudson, Kelly du Plessis, Melissa A Haendel, Phillip Wilcox, Sally Ann Lynch, Shamir Rind, Simon Easteal, Xavier Estivil, Nadine Caron, Meck Chongo, Yarlalu Thomas, Mary Catherine V Letinturier, Barend Christiaan Vorster
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature genetics (2024)
Rudrarup Bhattacharjee, Lachlan A Jolly, Mark A Corbett, Ing Chee Wee, Sushma R Rao, Alison E Gardner, Tarin Ritchie, Eline J H van Hugte, Ummi Ciptasari, Sandra G Piltz, Jacqueline E Noll, Nazzmer Nazri, Clare L van Eyk, Melissa White, Dani Fornarino, Cathryn Poulton, Gareth S Baynam, Lyndsey E Collins-Praino, Marten F Snel, Nael Nadif Kasri, Kim M Hemsley, Paul Q Thomas, Raman Kumar, Jozef Gecz
Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment. Nature communications 15 (1) (2024)
Matthew Silcocks, Ashley Farlow, Azure Hermes, Georgia Tsambos, Hardip R Patel, Sharon Huebner, Gareth S Baynam, Misty R Jenkins, Damjan Vukcevic, Simon Easteal, Stephen Leslie, null null
Indigenous Australian genomes show deep structure and rich novel variation. Nature (2023)
Cassandra MacArthur, Michele Hansen, Gareth S Baynam, Carol Bower, Erin A Kelty
Trends in prenatal diagnosis of congenital anomalies in Western Australia between 1980 and 2020: A population-based study. Paediatric and perinatal epidemiology (2023)
Andre L M Reis, Melissa Rapadas, Jillian M Hammond, Hasindu Gamaarachchi, Igor Stevanovski, Meutia Ayuputeri Kumaheri, Sanjog R Chintalaphani, Duminda S B Dissanayake, Owen M Siggs, Alex W Hewitt, Bastien Llamas, Alex Brown, Gareth S Baynam, Graham J Mann, Brendan J McMorran, Simon Easteal, Azure Hermes, Misty R Jenkins, null null, Hardip R Patel, Ira W Deveson
The landscape of genomic structural variation in Indigenous Australians. Nature (2023)
Birute Tumiene, Harm Peters, Bela Melegh, Borut Peterlin, Algirdas Utkus, Natalja Fatkulina, György Pfliegler, Holm Graessner, Sanja Hermanns, Maurizio Scarpa, Jean-Yves Blay, Sharon Ashton, Lucy McKay, Gareth S Baynam
Rare disease education in Europe and beyond: time to act. Orphanet journal of rare diseases 17 (1) (2022)
Birute Tumiene, Harm Peters, Bela Melegh, Borut Peterlin, Algirdas Utkus, Natalja Fatkulina, György Pfliegler, Holm Graessner, Sanja Hermanns, Maurizio Scarpa, Jean-Yves Blay, Sharon Ashton, Lucy McKay, Gareth S Baynam
Rare disease education in Europe and beyond: time to act. Orphanet journal of rare diseases 17 (1) (2022)
Birute Tumiene, Harm Peters, Bela Melegh, Borut Peterlin, Algirdas Utkus, Natalja Fatkulina, György Pfliegler, Holm Graessner, Sanja Hermanns, Maurizio Scarpa, Jean-Yves Blay, Sharon Ashton, Lucy McKay, Gareth S Baynam
Rare disease education in Europe and beyond: time to act. Orphanet journal of rare diseases 17 (1) (2022)
Joanne Luke, Philippa Dalach, Lindsay Tuer, Ravi Savarirayan, Angeline Ferdinand, Julie McGaughran, Emma Kowal, Libby Massey, Gail Garvey, Hugh Dawkins, Misty R Jenkins, Yin Paradies, Glenn Pearson, Chloe A Stutterd, Gareth S Baynam, Margaret Kelaher
Investigating disparity in access to Australian clinical genetic health services for Aboriginal and Torres Strait Islander people. Nature communications 13 (1) (2022)
Birute Tumiene, Harm Peters, Bela Melegh, Borut Peterlin, Algirdas Utkus, Natalja Fatkulina, György Pfliegler, Holm Graessner, Sanja Hermanns, Maurizio Scarpa, Jean-Yves Blay, Sharon Ashton, Lucy McKay, Gareth S Baynam
Rare disease education in Europe and beyond: time to act. Orphanet journal of rare diseases 17 (1) (2022)
Julius O B Jacobsen, Michael Baudis, Gareth S Baynam, Jacques S Beckmann, Sergi Beltran, Orion J Buske, Tiffany J Callahan, Christopher G Chute, Mélanie Courtot, Daniel Danis, Olivier Elemento, Andrea Essenwanger, Robert R Freimuth, Michael A Gargano, Tudor Groza, Ada Hamosh, Nomi L Harris, Rajaram Kaliyaperumal, Kevin C Kent Lloyd, Aly Khalifa, Peter M Krawitz, Sebastian Köhler, Brian J Laraway, Heikki Lehväslaiho, Leslie Matalonga, Julie A McMurry, Alejandro Metke-Jimenez, Christopher J Mungall, Monica C Munoz-Torres, Soichi Ogishima, Anastasios Papakonstantinou, Davide Piscia, Nikolas Pontikos, Núria Queralt-Rosinach, Marco Roos, Julian Sass, Paul N Schofield, Dominik Seelow, Anastasios Siapos, Damian Smedley, Lindsay D Smith, Robin Steinhaus, Jagadish Chandrabose Sundaramurthi, Emilia M Swietlik, Sylvia Thun, Nicole A Vasilevsky, Alex H Wagner, Jeremy L Warner, Claus Weiland, null null, Melissa A Haendel, Peter Nick Robinson
The GA4GH Phenopacket schema defines a computable representation of clinical data. Nature biotechnology 40 (6) (2022)
Lisa Matthews, Vaughan Chin, Marisa Taliangis, Amanda Samanek, Gareth S Baynam
Childhood rare diseases and the UN convention on the rights of the child. Orphanet journal of rare diseases 16 (1) (2021)
Gareth S Baynam, Stephen Groft, Francois Hendrikus van der Westhuizen, Safiyya D Gassman, Kelly du Plessis, Emily P Coles, Eda Selebatso, Moses Selebatso, Boikobo Gaobinelwe, Tebogo Selebatso, Dipesalema Joel, Virginia A Llera, Barend Christiaan Vorster, Barbara Wuebbels, Benjamin Djoudalbaye, Christopher P Austin, Judit Kumuthini, John Forman, Petra Kaufmann, James Chipeta, Désirée Gavhed, Annika Larsson, Maja Stojiljkovic, Ann Nordgren, Emilio J A Roldan, Domenica Taruscio, Durhane Wong-Rieger, Kristen Nowak, Gemma A Bilkey, Simon Easteal, Sarah Bowdin, Juergen K V Reichardt, Sergi Beltran, Kenjiro Kosaki, Clara D M van Karnebeek, Mengchun Gong, Zhang Shuyang, Ruty Mehrian-Shai, David R Adams, Ratna D Puri, Feng Zhang, Nicholas Pachter, Maximilian Muenke, Christoffer Nellaker, William A Gahl, Helene Cederroth, Stephanie Broley, Maryke Schoonen, Kym M Boycott, Manuel Posada-de-la-Paz
A call for global action for rare diseases in Africa. Nature genetics 52 (1) (2020)
Maui Hudson, Nanibaa' A Garrison, Rogena Sterling, Nadine R Caron, Keolu Fox, Joseph Yracheta, Jane Anderson, Phil Wilcox, Laura Arbour, Alex Brown, Maile Taualii, Tahu Kukutai, Rodney Haring, Ben Te Aika, Gareth S Baynam, Peter K Dearden, David Chagne, Ripan S Malhi, Ibrahim Garba, Nicki Tiffin, Deborah A Bolnick, Matthew B Stott, Anna K Rolleston, Leah L Ballantyne, Ray Lovett, Dominique David-Chavez, Andrew Martinez, Andrew Sporle, Maggie Walter, Jeff Reading, Stephanie Russo Carroll
Rights, interests and expectations: Indigenous perspectives on unrestricted access to genomic data. Nature reviews. Genetics 21 (6) (2020)
Nicole A Vasilevsky, Erin D Foster, Mark E Engelstad, Leigh C Carmody, Matt Might, Chip Chambers, Hugh J S Dawkins, Janine Lewis, Maria G Della Rocca, Michelle Snyder, Cornelius F Boerkoel, Ana Rath, Sharon F Terry, Alastair Kent, Beverly Searle, Gareth S Baynam, Erik Jones, Pam Gavin, Michael Bamshad, Jessica Xiao-Ling Chong, Tudor Groza, David R Adams, Adam C Resnick, Allison P Heath, Chris Mungall, Ingrid A Holm, Kayli Rageth, Catherine A Brownstein, Kent Shefchek, Julie A McMurry, Peter Nick Robinson, Sebastian Koehler, Melissa A Haendel
Plain-language medical vocabulary for precision diagnosis. Nature genetics 50 (4) (2019)
Katrine Marie Johannesen, Diana Mitter, Robert Janowski, Christian Roth, Joseph Toulouse, Anne-Lise Poulat, Dorothee M Ville, Nicolas Chatron, Eva H Brilstra, Karin Geleijns, Alfred Peter Born, Scott McLean, Kimberly Nugent, Gareth S Baynam, Cathryn Poulton, Lauren Dreyer, Dylan Gration, Solveig Schulz, Andrea Dieckmann, Katherine L Helbig, Andreas Merkenschlager, Rami Abou Jamra, Anja Finck, Elena Gardella, Henrik Hjalgrim, Ghayda M Mirzaa, Francesco Brancati, Tatjana Bierhals, Jonas Denecke, Maja Hempel, Johannes R Lemke, Guido Rubboli, Petra Muschke, Renzo Guerrini, Annalisa Vetro, Dierk Niessing, Gaëtan Lesca, Rikke Steensjerre Moller
Defining and expanding the phenotype of QARS-associated developmental epileptic encephalopathy. Neurology. Genetics 5 (6) (2019)
Denise Anderson, Gareth S Baynam, Jenefer M Blackwell, Timo Lassmann
Personalised analytics for rare disease diagnostics. Nature communications 10 (1) (2019)

Gareth S Baynam.css-eqlu8i{font-size:small;padding-left:4px;} (Gareth Baynam)

Publication Activity (10 Years)

Top Topics

Top Venues

Gareth S Baynam (Gareth Baynam)