Ho-Ming Luk (Luk Ho-Ming, Ho M Luk, Ho Ming Luk)

ORCID

Publication Activity (10 Years)

Years Active: 2016-2022
Publications (10 Years): 22

Top Venues

American journal of medical genetics. Part A

Case reports in genetics

Annals of neurology

Genes

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

Publications

Stephanie Ho, Ho-Ming Luk, Ivan F M Lo
KBG syndrome in a Chinese population: A case series. American journal of medical genetics. Part A 188 (6) (2022)
Pui Tak Yu, Wendy Shu, Sau-Lan Mok, Pui-Wah Hui, Lin-Wai Chan, Ka-Yin Kwok, Kelvin Yuen Kwong Chan, Tsz-Kin Lo, Brian Hon-Yin Chung, Ho-Ming Luk, Anita Sik Yau Kan
Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome-An unexpected diagnosis of androgenetic chimera and its clinical implications. American journal of medical genetics. Part A 188 (5) (2022)
Po Lam So, Shuk Yi Annie Hui, Teresa Wei Ling Ma, Wendy Shu, Amelia Pui Wah Hui, Choi Wah Kong, Tsz Kin Lo, Amanda Nim Chi Kan, Elaine Yee Ling Kan, Josephine Shuk Ching Chong, Brian Hon Yin Chung, Ho-Ming Luk, Kwong-Wai Choy, Anita Sik Yau Kan, Wing Cheong Leung
Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies. Genes 13 (11) (2022)
Janet Ling, Wai Lan Yeung, Kam Lun Ellis Hon, Ivan F M Lo, Ho-Ming Luk, Cheuk Wing Fung, Alexander K C Leung
Successful Treatment of Drug-Resistant Seizures Secondary to Ring 20 Mosaicism with Perampanel as an Add-On Antiepileptic Drug. Case reports in pediatrics 2022 (2022)
Stephanie Ho, Ho-Ming Luk, Ivan F M Lo
The first case report of Strømme syndrome in a Chinese patient: Expanding the phenotype and literature review. American journal of medical genetics. Part A 188 (5) (2022)
Shirley S W Cheng, Ho-Ming Luk, Ivan F M Lo
An adult Chinese patient with developmental delay with short stature, dysmorphic features, and sparse hair (Loucks-Innes syndrome). American journal of medical genetics. Part A 185 (6) (2021)
Stephanie Ho, Ho-Ming Luk, Ivan F M Lo
Extending the phenotype of DeSanto-Shinawi syndrome: A case report and literature review. American journal of medical genetics. Part A (2021)
Shirley S W Cheng, Ho-Ming Luk, Myth Tsz-Shun Mok, Sha-Sha Leung, Ivan F M Lo
Genotype and phenotype in 18 Chinese patients with Coffin-Siris syndrome. American journal of medical genetics. Part A 185 (7) (2021)
Po Lam So, Ho-Ming Luk, Kris P T Yu, Shirley S W Cheng, Edgar W L Hau, Stephanie K L Ho, Stephen T S Lam, Ivan F M Lo
Clinical and molecular characterization study of Chinese Kabuki syndrome in Hong Kong. American journal of medical genetics. Part A 185 (3) (2020)
Pui Tak Yu, Ho-Ming Luk, Ivan F M Lo
Rubinstein-Taybi syndrome in Chinese population with four novel mutations. American journal of medical genetics. Part A 185 (1) (2020)
Pui Tak Yu, Ho-Ming Luk, Myth T Mok, Fm Ivan Lo
Evolving clinical manifestations of mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome: From infancy to adulthood in a 31-year-old woman. American journal of medical genetics. Part A 185 (3) (2020)
Mimi Tin Yan Seto, Aida M Bertoli-Avella, Ka Wang Cheung, Kelvin Yuen-Kwong Chan, Kit San Yeung, Jasmine Lee-Fong Fung, Christian Beetz, Peter Bauer, Ho-Ming Luk, Ivan Fai-Man Lo, Chin Peng Lee, Brian Hon-Yin Chung, Anita Sik-Yau Kan
Prenatal and postnatal diagnosis of Schuurs-Hoeijmakers syndrome: Case series and review of the literature. American journal of medical genetics. Part A 185 (2) (2020)
Cedrik Tekendo-Ngongang, Babajide Owosela, Nicole Fleischer, Yonit A Addissie, Bryan Malonga, Ebenezer Badoe, Neerja Gupta, Angélica Moresco, Victoria Huckstadt, Engy A Ashaat, Dalia Farouk Hussen, Ho-Ming Luk, Ivan F M Lo, Brian Hon-Yin Chung, Jasmine L F Fung, Danilo Moretti-Ferreira, Letícia Cassimiro Batista, Stephanie Lotz-Esquivel, Manuel Saborio-Rocafort, Ramses Badilla-Porras, Monica Penon-Portmann, Kelly L Jones, Omar A Abdul-Rahman, Annette Uwineza, Eloise J Prijoles, Ifeanyi Kanayo Ifeorah, Arianne Llamos Paneque, Nirmala D Sirisena, Leah Ke'ala'aumoe Dowsett, Sansan Lee, Gerarda Cappuccio, Carolyn Sian Kitchin, Alicia Diaz-Kuan, Meow-Keong Thong, María Gabriela Obregon, Leon Mutesa, Vajira H W Dissanayake, Mona O El Ruby, Nicola Brunetti-Pierri, Ekanem Nsikak Ekure, Roger E Stevenson, Maximilian Muenke, Paul S Kruszka
Rubinstein-Taybi syndrome in diverse populations. American journal of medical genetics. Part A 182 (12) (2020)
Shirley S W Cheng, Pui Kwan Joyce Chan, Ho-Ming Luk, Myth Tsz-Shun Mok, Ivan F M Lo
Adult Chinese twins with Kenny-Caffey syndrome type 2: A potential age-dependent phenotype and review of literature. American journal of medical genetics. Part A 185 (2) (2020)
Emily C Oates, Kristi J Jones, Sandra Donkervoort, Amanda Charlton, Susan Brammah, John Edward Smith, James S Ware, Kyle S Yau, Lindsay C Swanson, Nicola Whiffin, Anthony J Peduto, Adam M Bournazos, Leigh B Waddell, Michelle A Farrar, Hugo A Sampaio, Hooi Ling Teoh, Phillipa J Lamont, David Mowat, Robin B Fitzsimons, Alastair J Corbett, Monique M Ryan, Gina L O'Grady, Sarah A Sandaradura, Roula Ghaoui, Himanshu Joshi, Jamie L Marshall, Melinda A Nolan, Simranpreet Kaur, Jaya Punetha, Ana Töpf, Elizabeth Harris, Madhura Bakshi, Casie A Genetti, Minttu Marttila, Ulla Werlauff, Nathalie Streichenberger, Alan Pestronk, Ingrid Mazanti, Jason R Pinner, Carole Vuillerot, Carla Grosmann, Ana Camacho, Payam Mohassel, Meganne E Leach, A Reghan Foley, Diana Bharucha-Goebel, James Collins, Anne M Connolly, Heather R Gilbreath, Susan T Iannaccone, Diana Castro, Beryl B Cummings, Richard I Webster, Leïla Lazaro, John Vissing, Sandra Coppens, Nicolas Deconinck, Ho-Ming Luk, Neil H Thomas, Nicola C Foulds, Marjorie A Illingworth, Sian Ellard, Catriona A McLean, Rahul Phadke, Gianina Ravenscroft, Nanna Witting, Peter Hackman, Isabelle Richard, Sandra T Cooper, Erik-Jan Kamsteeg, Eric P Hoffman, Kate Bushby, Volker Straub, Bjarne Udd, Ana Ferreiro, Kathryn N North, Nigel F Clarke, Monkol Lek, Alan H Beggs, Carsten G Bönnemann, Daniel G MacArthur, Henk Granzier, Mark R Davis, Nigel G Laing
Congenital Titinopathy: Comprehensive characterization and pathogenic insights. Annals of neurology 83 (6) (2019)
Shirley S W Cheng, Ho-Ming Luk, David K H Chan, Ivan F M Lo
CHARGE syndrome in nine patients from China. American journal of medical genetics. Part A 182 (1) (2019)
Paul S Kruszka, Antonio R Porras, Deise Helena de Souza, Angélica Moresco, Victoria Huckstadt, Ashleigh D Gill, Alec P Boyle, Tommy Hu, Yonit A Addissie, Gary T K Mok, Cedrik Tekendo-Ngongang, Karen Fieggen, Eloise J Prijoles, Pranoot Tanpaiboon, Engela Honey, Ho-Ming Luk, Ivan F M Lo, Meow-Keong Thong, Premala Muthukumarasamy, Kelly L Jones, Khadija Belhassan, Karim Ouldim, Ihssane El Bouchikhi, Laila Bouguenouch, Anju Shukla, Katta Mohan Girisha, Nirmala D Sirisena, Vajira H W Dissanayake, C Sampath Paththinige, Rupesh Mishra, Monisha S Kisling, Carlos R Ferreira, María Beatriz de Herreros, Ni-Chung Lee, Saumya S Jamuar, Angeline Lai, Ee Shien Tan, Jiin Ying Lim, Cham Breana Wen-Min, Neerja Gupta, Stephanie Lotz-Esquivel, Ramsés Badilla-Porras, Dalia Farouk Hussen, Mona O El Ruby, Engy A Ashaat, Siddaramappa Jagdish Patil, Leah Dowsett, Alison Eaton, A Micheil Innes, Vorasuk Shotelersuk, Ëben Badoe, Ambroise Wonkam, María Gabriela Obregon, Brian H Y Chung, Milana Trubnykova, Jorge La Serna, Bertha Elena Gallardo Jugo, Miguel Chávez Pastor, Hugo Hernán Abarca Barriga, Andre Megarbane, Beth A Kozel, Mieke M van Haelst, Roger E Stevenson, Marshall Summar, A Adebowale Adeyemo, Colleen A Morris, Danilo Moretti-Ferreira, Marius George Linguraru, Maximilian Muenke
Williams-Beuren syndrome in diverse populations. American journal of medical genetics. Part A 176 (5) (2019)
Deepika D'Cunha Burkardt, Anna Zachariou, Chey Loveday, Clare L Allen, David J Amor, Anna Ardissone, Siddharth Banka, Alexia Bourgois, Christine Coubes, Cheryl Cytrynbaum, Laurence Olivier-Faivre, Gerard Marion, Rachel Horton, Dieter Kotzot, Guillermo Lay-Son, Melissa Lees, Karen Jaqueline Low, Ho-Ming Luk, Paul Mark, Allyn McConkie-Rosell, Marie McDonald, John G Pappas, Christophe Phillipe, Deborah Shears, Brian Skotko, Fiona Stewart, Helen Stewart, I Karen Temple, Frederic T Mau-Them, Ricardo A Verdugo, Rosanna Weksberg, Yuri A Zarate, John M Graham, Katrina Tatton-Brown
HIST1H1E heterozygous protein-truncating variants cause a recognizable syndrome with intellectual disability and distinctive facial gestalt: A study to clarify the HIST1H1E syndrome phenotype in 30 individuals. American journal of medical genetics. Part A 179 (10) (2019)
Jasmine L F Fung, Kavitha Rethanavelu, Ho-Ming Luk, Matthew S P Ho, Ivan F M Lo, Brian Hon-Yin Chung
Coffin-Lowry syndrome in Chinese. American journal of medical genetics. Part A 179 (10) (2019)
Kavitha Rethanavelu, Jasmine L F Fung, Jeffrey F T Chau, Steven L C Pei, Claudia C Y Chung, Christopher C Y Mak, Ho-Ming Luk, Brian H Y Chung
Phenotypic and mutational spectrum of 21 Chinese patients with Alström syndrome. American journal of medical genetics. Part A 182 (2) (2019)
Laura M McDonell, Gordon Ka-Chun Leung, Hussein Daoud, Janice Ip, Stella Chim, Ho-Ming Luk, Lawrence Lan, null null, Kym M Boycott, Brian Hon-Yin Chung
Mosaic KRAS mutation in a patient with encephalocraniocutaneous lipomatosis and renovascular hypertension. American journal of medical genetics. Part A 176 (11) (2018)
Ho-Ming Luk
Adult Prader-Willi Syndrome: An Update on Management. Case reports in genetics 2016 (2016)

Ho-Ming Luk.css-eqlu8i{font-size:small;padding-left:4px;} (Luk Ho-Ming, Ho M Luk, Ho Ming Luk)

Publication Activity (10 Years)

Top Topics

Top Venues

Ho-Ming Luk (Luk Ho-Ming, Ho M Luk, Ho Ming Luk)