Hamish S Scott (Hamish Scott)

Scopus Author ID ResearcherID Loop profile Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2015-2023
Publications (10 Years): 44

Top Venues

SA Pathology

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

Affiliation History

SA Pathology Jul 1o 2009

Australia

Head of Department :: Department of Genetics and Molecular Pathology

Publications

Jan Kazenwadel, Parvathy Venugopal, Anna Oszmiana, John Toubia, Luis Alberto Arriola-Martinez, Virginia Panara, Sandra G Piltz, Chris Brown, Wanshu Ma, Andreas W Schreiber, Katarzyna Koltowska, Samir Taoudi, Paul Q Thomas, Hamish S Scott, Natasha L Harvey
A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature. Nature 614 (7947) (2023)
Jan Kazenwadel, Parvathy Venugopal, Anna Oszmiana, John Toubia, Luis Alberto Arriola-Martinez, Virginia Panara, Sandra G Piltz, Chris Brown, Wanshu Ma, Andreas W Schreiber, Katarzyna Koltowska, Samir Taoudi, Paul Q Thomas, Hamish S Scott, Natasha L Harvey
A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature. Nature 614 (7947) (2023)
Alicia B Byrne, Peer Arts, Thuong T Ha, Karin S Kassahn, Lynn S Pais, Anne H O'Donnell-Luria, null null, Milena Babic, Mahalia S B Frank, Jinghua Feng, Paul Wang, David Michael Lawrence, Leila Eshraghi, Luis Alberto Arriola-Martinez, John Toubia, Hung Nguyen, null null, George McGillivray, Jason Pinner, Fiona McKenzie, Rebecca Morrow, Jill Lipsett, Nick Manton, Teck Yee Khong, Lynette Moore, Jan E Liebelt, Andreas W Schreiber, Sarah L King-Smith, Tristan S E Hardy, Matilda R Jackson, Christopher P Barnett, Hamish S Scott
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death. Nature medicine 29 (1) (2023)
Alicia B Byrne, Peer Arts, Thuong T Ha, Karin S Kassahn, Lynn S Pais, Anne H O'Donnell-Luria, null null, Milena Babic, Mahalia S B Frank, Jinghua Feng, Paul Wang, David Michael Lawrence, Leila Eshraghi, Luis Alberto Arriola-Martinez, John Toubia, Hung Nguyen, null null, George McGillivray, Jason Pinner, Fiona McKenzie, Rebecca Morrow, Jill Lipsett, Nick Manton, Teck Yee Khong, Lynette Moore, Jan E Liebelt, Andreas W Schreiber, Sarah L King-Smith, Tristan S E Hardy, Matilda R Jackson, Christopher P Barnett, Hamish S Scott
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death. Nature medicine 29 (1) (2023)
Alicia B Byrne, Peer Arts, Thuong T Ha, Karin S Kassahn, Lynn S Pais, Anne H O'Donnell-Luria, null null, Milena Babic, Mahalia S B Frank, Jinghua Feng, Paul Wang, David Michael Lawrence, Leila Eshraghi, Luis Alberto Arriola-Martinez, John Toubia, Hung Nguyen, null null, George McGillivray, Jason Pinner, Fiona McKenzie, Rebecca Morrow, Jill Lipsett, Nick Manton, Teck Yee Khong, Lynette Moore, Jan E Liebelt, Andreas W Schreiber, Sarah L King-Smith, Tristan S E Hardy, Matilda R Jackson, Christopher P Barnett, Hamish S Scott
Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death. Nature medicine (2023)
Jan Kazenwadel, Parvathy Venugopal, Anna Oszmiana, John Toubia, Luis Alberto Arriola-Martinez, Virginia Panara, Sandra G Piltz, Chris Brown, Wanshu Ma, Andreas W Schreiber, Katarzyna Koltowska, Samir Taoudi, Paul Q Thomas, Hamish S Scott, Natasha L Harvey
A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature. Nature 614 (7947) (2023)
Jan Kazenwadel, Parvathy Venugopal, Anna Oszmiana, John Toubia, Luis Alberto Arriola-Martinez, Virginia Panara, Sandra G Piltz, Chris Brown, Wanshu Ma, Andreas W Schreiber, Katarzyna Koltowska, Samir Taoudi, Paul Q Thomas, Hamish S Scott, Natasha L Harvey
A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature. Nature (2023)
Jan Kazenwadel, Parvathy Venugopal, Anna Oszmiana, John Toubia, Luis Alberto Arriola-Martinez, Virginia Panara, Sandra G Piltz, Chris Brown, Wanshu Ma, Andreas W Schreiber, Katarzyna Koltowska, Samir Taoudi, Paul Q Thomas, Hamish S Scott, Natasha L Harvey
A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature. Nature 614 (7947) (2023)
Devendra K Hiwase, Christopher N Hahn, Elizabeth Ngoc Hoa Tran, Rakchha Chhetri, Anmol Baranwal, Aref A Al-Kali, Kirsty Sharplin, Dariusz Ladon, Rachel Hollins, Patricia T Greipp, Monika Kutyna, Hassan Alkhateeb, Talha Badar, Paul Wang, David Morrall Ross, Deepak Singhal, Naranie Shanmuganathan, Peter Bardy, Ashanka Beligaswatte, David Yeung, Mark R Litzow, Abhishek Mangaonkar, Pratyush Giri, Cindy Lee, Angie Yong, Noemi Horvath, Nimit Singhal, Raghu Gowda, William Hogan, Naseema Gangat, Mirinal S Patnaik, Kebede H Begna, Ing Soo Tiong, Andrew H Wei, Sharad Kumar, Anna L Brown, Hamish S Scott, Daniel Thomas, Chung H Kok, Ayalew Tefferi, Mithun Vinod Shah
TP53 mutation in therapy-related myeloid neoplasm defines a distinct molecular subtype. Blood 141 (9) (2023)
Alicia B Byrne, Peer Arts, Thuong T Ha, Karin S Kassahn, Lynn S Pais, Anne H O'Donnell-Luria, null null, Milena Babic, Mahalia S B Frank, Jinghua Feng, Paul Wang, David Michael Lawrence, Leila Eshraghi, Luis Alberto Arriola-Martinez, John Toubia, Hung Nguyen, null null, George McGillivray, Jason Pinner, Fiona McKenzie, Rebecca Morrow, Jill Lipsett, Nick Manton, Teck Yee Khong, Lynette Moore, Jan E Liebelt, Andreas W Schreiber, Sarah L King-Smith, Tristan S E Hardy, Matilda R Jackson, Christopher P Barnett, Hamish S Scott
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death. Nature medicine (2023)
Claire C Homan, Hamish S Scott, Anna L Brown
Hereditary platelet disorders associated with germline variants in RUNX1, ETV6 and ANKRD26. Blood (2023)
Dominyka Batkovskyte, Fiona McKenzie, Fulya Taylan, Pelin Ozlem Simsek-Kiper, Sarah M Nikkel, Hirofumi Ohashi, Roger E Stevenson, Thuong Ha, Denise P Cavalcanti, Hiroyuki Miyahara, Steven A Skinner, Miguel A Aguirre, Zühal Akçören, Gulen Eda Utine, Tillie Chiu, Kenji Shimizu, Anna Hammarsjö, Koray Boduroglu, Hannah W Moore, Raymond J Louie, Peer Arts, Allie N Merrihew, Milena Babic, Matilda R Jackson, Nikos Papadogiannakis, Anna Lindstrand, Ann Nordgren, Christopher P Barnett, Hamish S Scott, Andrei S Chagin, Gen Nishimura, Giedre Grigelioniene
Al-Gazali skeletal dysplasia constitutes the lethal end of ADAMTSL2-related disorders. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research (2023)
Jan Kazenwadel, Parvathy Venugopal, Anna Oszmiana, John Toubia, Luis Alberto Arriola-Martinez, Virginia Panara, Sandra G Piltz, Chris Brown, Wanshu Ma, Andreas W Schreiber, Katarzyna Koltowska, Samir Taoudi, Paul Q Thomas, Hamish S Scott, Natasha L Harvey
A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature. Nature (2023)
Claire C Homan, Michael W Drazer, Kai Yu, David Michael Lawrence, Jinghua Feng, Luis Alberto Arriola-Martinez, Matthew J Pozsgai, Kelsey E McNeely, Thuong Thi Ha, Parvathy Venugopal, Peer Arts, Sarah King-Smith, Jesse Jc Cheah, Mark Armstrong, Paul Wang, Csaba Bödör, Alan B Cantor, Mario Cazzola, Erin S Degelman, Courtney D Di Nardo, Nicolas Duployez, Rémi Favier, Stefan Fröhling, Ana Rio-Machin, Jeffery M Klco, Alwin Krämer, Mineo Kurokawa, Joanne Lee, Luca Malcovati, Neil V Morgan, Natsoulis Georges, Carolyn Owen, Keyur Pravinchandra Patel, Claude Preudhomme, Hana Raslova, Hugh Young Rienhoff, Tim Ripperger, Rachael R Schulte, Kiran Tawana, Elvira Velloso, Yan Benedict, Erika Mijin Kwon Kim, Raman Sood, Amy P Hsu, Steven M Holland, Kerry Phillips, Nicola Poplawski, Milena Babic, Andrew H Wei, Cecily J Forsyth, Helen Mar Fan, Ian Lewis, Julian P Cooney, Rachel Susman, Lucy C Fox, Piers Blombery, Deepak Singhal, Devendra K Hiwase, Belinda Phipson, Andreas W Schreiber, Christopher N Hahn, Hamish S Scott, Paul P Liu, Lucy A Godley, Anna L Brown
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germ line RUNX1, GATA2, and DDX41 variants. Blood advances (2023)
Sebastian Lunke, Sophie E Bouffler, Chirag V Patel, Sarah A Sandaradura, Meredith Wilson, Jason Pinner, Matthew F Hunter, Christopher P Barnett, Mathew Wallis, Benjamin Kamien, Tiong Yang Tan, Mary-Louise Freckmann, Belinda Chong, Dean Phelan, David Francis, Karin S Kassahn, Thuong T Ha, Song Gao, Peer Arts, Matilda R Jackson, Hamish S Scott, Stefanie Eggers, Simone Rowley, Kirsten Boggs, Ana Rakonjac, Gemma R Brett, Michelle G de Silva, Amanda Springer, Michelle Ward, Kirsty Stallard, Cas Simons, Thomas Conway, Andreas Halman, Nicole J Van Bergen, Tim Sikora, Liana N Semcesen, David A Stroud, Alison G Compton, David R Thorburn, Katrina M Bell, Simon Sadedin, Kathryn N North, John Chrisodoulou, Zornitza Stark
Integrated multi-omics for rapid rare disease diagnosis on a national scale. Nature medicine (2023)
Jan Kazenwadel, Parvathy Venugopal, Anna Oszmiana, John Toubia, Luis Alberto Arriola-Martinez, Virginia Panara, Sandra G Piltz, Chris Brown, Wanshu Ma, Andreas W Schreiber, Katarzyna Koltowska, Samir Taoudi, Paul Q Thomas, Hamish S Scott, Natasha L Harvey
A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature. Nature 614 (7947) (2023)
Jan Kazenwadel, Parvathy Venugopal, Anna Oszmiana, John Toubia, Luis Alberto Arriola-Martinez, Virginia Panara, Sandra G Piltz, Chris Brown, Wanshu Ma, Andreas W Schreiber, Katarzyna Koltowska, Samir Taoudi, Paul Q Thomas, Hamish S Scott, Natasha L Harvey
A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature. Nature (2023)
Jan Kazenwadel, Parvathy Venugopal, Anna Oszmiana, John Toubia, Luis Alberto Arriola-Martinez, Virginia Panara, Sandra G Piltz, Chris Brown, Wanshu Ma, Andreas W Schreiber, Katarzyna Koltowska, Samir Taoudi, Paul Q Thomas, Hamish S Scott, Natasha L Harvey
A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature. Nature 614 (7947) (2023)
Claire C Homan, Hamish S Scott, Anna L Brown
Hereditary platelet disorders associated with germline variants in RUNX1, ETV6 and ANKRD26. Blood (2023)
Devendra K Hiwase, Christopher N Hahn, Elizabeth Ngoc Hoa Tran, Rakchha Chhetri, Anmol Baranwal, Aref A Al-Kali, Kirsty Sharplin, Dariusz Ladon, Rachel Hollins, Patricia T Greipp, Monika Kutyna, Hassan Alkhateeb, Talha Badar, Paul Wang, David Morrall Ross, Deepak Singhal, Naranie Shanmuganathan, Peter Bardy, Ashanka Beligaswatte, David Yeung, Mark R Litzow, Abhishek Mangaonkar, Pratyush Giri, Cindy Lee, Angie Yong, Noemi Horvath, Nimit Singhal, Raghu Gowda, William Hogan, Naseema Gangat, Mirinal S Patnaik, Kebede H Begna, Ing Soo Tiong, Andrew H Wei, Sharad Kumar, Anna L Brown, Hamish S Scott, Daniel Thomas, Chung H Kok, Ayalew Tefferi, Mithun Vinod Shah
TP53 mutation in therapy-related myeloid neoplasm defines a distinct molecular subtype. Blood 141 (9) (2023)
Devendra K Hiwase, Christopher N Hahn, Elizabeth Ngoc Hoa Tran, Rakchha Chhetri, Anmol Baranwal, Aref A Al-Kali, Kirsty Sharplin, Dariusz Ladon, Rachel Hollins, Patricia T Greipp, Monika Kutyna, Hassan Alkhateeb, Talha Badar, Paul Wang, David Morrall Ross, Deepak Singhal, Naranie Shanmuganathan, Peter Bardy, Ashanka Beligaswatte, David Yeung, Mark R Litzow, Abhishek Mangaonkar, Pratyush Giri, Cindy Lee, Angie Yong, Noemi Horvath, Nimit Singhal, Raghu Gowda, William Hogan, Naseema Gangat, Mirinal S Patnaik, Kebede H Begna, Ing Soo Tiong, Andrew H Wei, Sharad Kumar, Anna L Brown, Hamish S Scott, Daniel Thomas, Chung H Kok, Ayalew Tefferi, Mithun Vinod Shah
TP53 mutation in therapy-related myeloid neoplasm defines a distinct molecular subtype. Blood 141 (9) (2023)
Alicia B Byrne, Peer Arts, Thuong T Ha, Karin S Kassahn, Lynn S Pais, Anne H O'Donnell-Luria, null null, Milena Babic, Mahalia S B Frank, Jinghua Feng, Paul Wang, David Michael Lawrence, Leila Eshraghi, Luis Alberto Arriola-Martinez, John Toubia, Hung Nguyen, null null, George McGillivray, Jason Pinner, Fiona McKenzie, Rebecca Morrow, Jill Lipsett, Nick Manton, Teck Yee Khong, Lynette Moore, Jan E Liebelt, Andreas W Schreiber, Sarah L King-Smith, Tristan S E Hardy, Matilda R Jackson, Christopher P Barnett, Hamish S Scott
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death. Nature medicine 29 (1) (2023)
Mithun Vinod Shah, Elizabeth Ngoc Hoa Tran, Syed Shah, Rakchha Chhetri, Anmol Baranwal, Dariusz Ladon, Carl Shultz, Aref Al-Kali, Anna L Brown, Dong Chen, Hamish S Scott, Patricia T Greipp, Daniel Thomas, Hassan B Alkhateeb, Deepak Singhal, Naseema Gangat, Sharad Kumar, Mirinal S Patnaik, Christopher N Hahn, Chung Hoow Kok, Ayalew Tefferi, Devendra K Hiwase
TP53 mutation variant allele frequency of ≥10% is associated with poor prognosis in therapy-related myeloid neoplasms. Blood cancer journal 13 (1) (2023)
Zijing Zhou, Xiaonuo Ma, Yiechang Lin, Delfine Cheng, Navid Bavi, Genevieve A Secker, Jinyuan Vero Li, Vaibhao Janbandhu, Drew L Sutton, Hamish S Scott, Mingxi Yao, Richard P Harvey, Natasha L Harvey, Ben Corry, Yixiao Zhang, Charles D Cox
MyoD-family inhibitor proteins act as auxiliary subunits of Piezo channels. Science (New York, N.Y.) 381 (6659) (2023)
Esra Yıldız Bölükbaşı, Justyna A Karolak, Przemyslaw Szafranski, Tomasz Gambin, Admire Matsika, Sam McManus, Hamish S Scott, Peer Arts, Thuong Ha, Christopher P Barnett, Jonathan Rodgers, Przemyslaw Szafranski
Variable expressivity in a four-generation ACDMPV family with a non-coding hypermorphic SNV in trans to the frameshifting FOXF1 variant. European journal of human genetics : EJHG 30 (10) (2022)
Alicia B Byrne, Pascal Brouillard, Drew L Sutton, Jan Kazenwadel, Saba Montazaribarforoushi, Genevieve A Secker, Anna Oszmiana, Milena Babic, Kelly L Betterman, Peter J Brautigan, Melissa White, Sandra G Piltz, Paul Q Thomas, Christopher N Hahn, Matthias Rath, Ute Felbor, G Christoph Korenke, Christopher L Smith, Kathleen H Wood, Sarah E Sheppard, Denise M Adams, Ariana Kariminejad, Raphaël Helaers, Laurence M Boon, Nicole Revencu, Lynette Moore, Christopher P Barnett, Eric Haan, Peer Arts, Miikka Vikkula, Hamish S Scott, Natasha L Harvey
Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema. Science translational medicine 14 (634) (2022)
Michael W Drazer, Claire C Homan, Kai Yu, Marcela Cavalcante de Andrade Silva, Kelsey E McNeely, Matthew J Pozsgai, Maria G Acevedo-Mendez, Jeremy P Segal, Peng Wang, Jinghua Feng, Sarah L King-Smith, Erika Kim, Sophia Claire Korotev, David Michael Lawrence, Andreas W Schreiber, Christopher N Hahn, Hamish S Scott, Raman Sood, null null, Elvira Deolinda Rodrigues Pereira Velloso, Anna L Brown, Paul P Liu, Lucy A Godley
Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations. Blood advances 6 (15) (2022)
Devendra K Hiwase, Christopher N Hahn, Elizabeth Ngoc Hoa Tran, Rakchha Chhetri, Anmol Baranwal, Aref A Al-Kali, Kirsty M Sharplin, Dariusz Ladon, Rachel Hollins, Patricia T Greipp, Monika M Kutyna, Hassan B Alkhateeb, Talha Badar, Paul Po-Shen Wang, David Morrall Ross, Deepak Singhal, Naranie Shanmuganathan, Peter G Bardy, Ashanka Beligaswatte, David T Yeung, Mark R Litzow, Abhishek A Mangaonkar, Pratyush Giri, Cindy H Lee, Angelina Yong, Noemi Horvath, Nimit Singhal, Raghu Gowda, William J Hogan, Naseema Gangat, Mirinal S Patnaik, Kebede H Begna, Ing Soo Tiong, Andrew H Wei, Sharad Kumar, Anna L Brown, Hamish S Scott, Daniel Thomas, Chung Hoow Kok, Ayalew Tefferi, Mithun Vinod Shah
TP53 mutation in therapy-related myeloid neoplasm defines a distinct molecular subtype. Blood (2022)
Devendra K Hiwase, Christopher N Hahn, Elizabeth Ngoc Hoa Tran, Rakchha Chhetri, Anmol Baranwal, Aref A Al-Kali, Kirsty M Sharplin, Dariusz Ladon, Rachel Hollins, Patricia T Greipp, Monika M Kutyna, Hassan B Alkhateeb, Talha Badar, Paul Po-Shen Wang, David Morrall Ross, Deepak Singhal, Naranie Shanmuganathan, Peter G Bardy, Ashanka Beligaswatte, David T Yeung, Mark R Litzow, Abhishek A Mangaonkar, Pratyush Giri, Cindy H Lee, Angelina Yong, Noemi Horvath, Nimit Singhal, Raghu Gowda, William J Hogan, Naseema Gangat, Mirinal S Patnaik, Kebede H Begna, Ing Soo Tiong, Andrew H Wei, Sharad Kumar, Anna L Brown, Hamish S Scott, Daniel Thomas, Chung Hoow Kok, Ayalew Tefferi, Mithun Vinod Shah
TP53 mutation in therapy-related myeloid neoplasm defines a distinct molecular subtype. Blood (2022)
Linjiang Lao, Isabelle Bourdeau, Lucia Gagliardi, Xiao He, Wei Shi, Bingbing Hao, Minjia Tan, Yan Hu, Junzheng Peng, Benoit Coulombe, David J Torpy, Hamish S Scott, Andre Lacroix, Hongyu Luo, Jiangping Wu
ARMC5 is part of an RPB1-specific ubiquitin ligase implicated in adrenal hyperplasia. Nucleic acids research 50 (11) (2022)
Caner Saygin, Gregory W Roloff, Christopher N Hahn, Rakchha Chhetri, Saar I Gill, Hany Elmariah, Chetasi Talati, Emma Nunley, Guimin Gao, Aelin Kim, Michael R Bishop, Satyajit Kosuri, Soma Das, Deepak Singhal, Parvathy Venugopal, Claire Christine Homan, Anna L Brown, Hamish S Scott, Devendra K Hiwase, Lucy A Godley
Allogeneic hematopoietic stem cell transplant outcomes in adults with inherited myeloid malignancies. Blood advances (2022)
Saumya E Samaraweera, Paul P S Wang, Ka Leung Li, Debora A Casolari, Jinghua Feng, Mark Pinese, Kyaw Ze Ya Maung, Paul Leo, Mark J Cowley, Kelly Perkins, Amanda M Smith, Jonathan Ellis, Amilia Wee, Devendra K Hiwase, Hamish S Scott, Andreas W Schreiber, Anna L Brown, Andrew J Deans, David Morrall Ross, Andrew S Moore, Thomas J Gonda, Christopher N Hahn, Richard J D'Andrea
Childhood acute myeloid leukemia shows a high level of germline predisposition. Blood 138 (22) (2022)
Claire C Homan, Parvathy Venugopal, Peer Arts, Nur H Shahrin, Simone K Feurstein, Lesley Rawlings, David Michael Lawrence, James Andrews, Sarah L King-Smith, Natasha L Harvey, Anna L Brown, Hamish S Scott, Christopher N Hahn
GATA2 deficiency syndrome: A decade of discovery. Human mutation 42 (11) (2021)
Deepak Singhal, Christopher N Hahn, Simone K Feurstein, Li Yan A Wee, Luke Moma, Monika M Kutyna, Rakchha Chhetri, Leila Eshraghi, Andreas W Schreiber, Jinghua Feng, Paul P-S Wang, Milena Babic, Wendy T Parker, Song Gao, Sarah Moore, Soma Das, David Thomas, Swetansu Pattnaik, Anna L Brown, Richard J D'Andrea, Nicola K Poplawski, Daniel Thomas, Hamish S Scott, Lucy A Godley, Devendra K Hiwase
Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer. Leukemia 35 (11) (2021)
Sunita M C De Sousa, John Toubia, Tristan S E Hardy, Jinghua Feng, Paul Wang, Andreas W Schreiber, Joel Geoghegan, Rachel Hall, Lesley Rawlings, Michael E Buckland, Catherine Luxford, Talia Novos, Roderick J Clifton-Bligh, Nicola K Poplawski, Hamish S Scott, David J Torpy
Aberrant Splicing of SDHC in Families With Unexplained Succinate Dehydrogenase-Deficient Paragangliomas. Journal of the Endocrine Society 4 (12) (2020)
Peer Arts, Jessica Garland, Alicia B Byrne, Tristan S E Hardy, Milena Babic, Jinghua Feng, Paul Wang, Thuong T Ha, Sarah L King-Smith, Andreas W Schreiber, April Crawford, Nick Manton, Lynette Moore, Christopher P Barnett, Hamish S Scott
Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndrome. American journal of medical genetics. Part A 182 (5) (2020)
Lucy C Fox, Michelle Tan, Anna L Brown, Peer Arts, Ella R Thompson, Georgina L Ryland, Jennifer Lickiss, Hamish S Scott, Nicola K Poplawski, Kerry Phillips, Neil A Came, Paul James, Stephen B Ting, David S Ritchie, Jeffrey Szer, Christopher N Hahn, Anthony Schwarer, Piers A Blombery
A synonymous GATA2 variant underlying familial myeloid malignancy with striking intrafamilial phenotypic variability. British journal of haematology 190 (5) (2020)
Parvathy Venugopal, Lucia Gagliardi, Cecily Forsyth, Jinghua Feng, Kerry Phillips, Milena Babic, Nicola K Poplawski, Hugh Young Rienhoff, Andreas W Schreiber, Christopher N Hahn, Anna L Brown, Hamish S Scott
Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss. BMC medical genetics 21 (1) (2020)
Daniel W Thomson, Nur Hezrin Shahrin, Paul P S Wang, Carol Wadham, Naranie Shanmuganathan, Hamish S Scott, Marcel E Dinger, Timothy P Hughes, Andreas W Schreiber, Susan Branford
Aberrant RAG-mediated recombination contributes to multiple structural rearrangements in lymphoid blast crisis of chronic myeloid leukemia. Leukemia 34 (8) (2020)
Alicia B Byrne, Peer Arts, Steven W Polyak, Jinghua Feng, Andreas W Schreiber, Karin S Kassahn, Christopher N Hahn, Dylan A Mordaunt, Janice M Fletcher, Jillian Lipsett, Drago Bratkovic, Grant W Booker, Nicholas J Smith, Hamish S Scott
Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6. NPJ genomic medicine 4 (2019)
Ilaria Iacobucci, Ji Wen, Manja Meggendorfer, John K Choi, Lei Shi, Stanley B Pounds, Catherine L Carmichael, Katherine E Masih, Sarah M Morris, R Coleman Lindsley, Laura J Janke, Thomas B Alexander, Guangchun Song, Chunxu Qu, Yongjin Li, Debbie Payne-Turner, Masanori Yoshida, Nobutaka Kiyokawa, Marcus Valentine, Virginia Valentine, Giuseppe Basso, Franco Locatelli, Eric J Enemark, Shirley K Y Kham, Allen Eng-Juh Yeoh, Xiaotu Ma, Xin Zhou, Edgar Sioson, Michael C Rusch, Rhonda E Ries, Elliot Stieglitz, Stephen P Hunger, Andrew H Wei, L Bik To, Ian D Lewis, Richard J D'Andrea, Benjamin T Kile, Anna L Brown, Hamish S Scott, Christopher N Hahn, Paula Marlton, Deqing Pei, Cheng Cheng, Mignon L Loh, Benjamin L Ebert, Soheil Meshinchi, Torsten Haferlach, Charles G Mullighan
Genomic subtyping and therapeutic targeting of acute erythroleukemia. Nature genetics 51 (4) (2019)
Han-Chung Lee, Hadri Hadi Md Yusof, Melody Pui-Yee Leong, Shahidee Zainal Abidin, Eryse Amira Seth, Chelsee A Hewitt, Sharmili Vidyadaran, Norshariza Binti Nordin, Hamish S Scott, Pike-See Cheah, King-Hwa Ling
Gene and protein expression profiles of JAK-STAT signalling pathway in the developing brain of the Ts1Cje down syndrome mouse model. The International journal of neuroscience 129 (9) (2019)
Jesse J C Cheah, Christopher N Hahn, Devendra K Hiwase, Hamish S Scott, Anna L Brown
Myeloid neoplasms with germline DDX41 mutation. International journal of hematology 106 (2) (2017)
Maya Lewinsohn, Anna L Brown, Luke M Weinel, Connie Phung, George Rafidi, Ming K Lee, Andreas W Schreiber, Jinghua Feng, Milena Babic, Chan-Eng Chong, Young Lee, Agnes Yong, Graeme K Suthers, Nicola Poplawski, Meryl Altree, Kerry Phillips, Louise Jaensch, Miriam Fine, Richard J D'Andrea, Ian D Lewis, Bruno C Medeiros, Daniel A Pollyea, Mary-Claire King, Tom Walsh, Siobán Keel, Akiko Shimamura, Lucy A Godley, Christopher N Hahn, Jane E Churpek, Hamish S Scott
Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies. Blood 127 (8) (2015)

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

Publication Activity (10 Years)

Top Topics

Top Venues

Hamish S Scott (Hamish Scott)