Wen-Hann Tan (W H Tan)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 19

Top Topics

Intellectual Disability

Psychometric Properties

Top Venues

American journal of medical genetics. Part A

Molecular genetics & genomic medicine

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

Publications

Bianca E Russell, Wen-Hann Tan
Chromatinopathies - from discovery to clinical diagnosis in the real world. Human genetics (2024)
Bianca E Russell, Wen-Hann Tan
Chromatinopathies - from discovery to clinical diagnosis in the real world. Human genetics 143 (4) (2024)
Bianca E Russell, Wen-Hann Tan
Chromatinopathies - from discovery to clinical diagnosis in the real world. Human genetics 143 (4) (2024)
Bianca E Russell, Rebecca R Kianmahd, Chelsea Munster, Anna Yu, Leena Ahad, Wen-Hann Tan
Clinical findings in 39 individuals with Bohring-Opitz syndrome from a global patient-driven registry with implications for tumor surveillance and recurrence risk. American journal of medical genetics. Part A 191 (4) (2023)
Bianca E Russell, Rebecca R Kianmahd, Chelsea Munster, Anna Yu, Leena Ahad, Wen-Hann Tan
Clinical findings in 39 individuals with Bohring-Opitz syndrome from a global patient-driven registry with implications for tumor surveillance and recurrence risk. American journal of medical genetics. Part A 191 (4) (2023)
Angela Gwaltney, Sarah Nelson Potter, Sarika U Peters, Rene L Barbieri-Welge, Lucia T Horowitz, Lisa M Noll, Rachel J Hundley, Lynne M Bird, Wen-Hann Tan, Anjali Sadhwani, Anne C Wheeler
Adaptive Skills of Individuals with Angelman Syndrome Assessed Using the Vineland Adaptive Behavior Scales, 2nd Edition. Journal of autism and developmental disorders (2023)
Bianca E Russell, Rebecca R Kianmahd, Chelsea Munster, Anna Yu, Leena Ahad, Wen-Hann Tan
Clinical findings in 39 individuals with Bohring-Opitz syndrome from a global patient-driven registry with implications for tumor surveillance and recurrence risk. American journal of medical genetics. Part A (2023)
Bianca E Russell, Rebecca R Kianmahd, Chelsea Munster, Anna Yu, Leena Ahad, Wen-Hann Tan
Clinical findings in 39 individuals with Bohring-Opitz syndrome from a global patient-driven registry with implications for tumor surveillance and recurrence risk. American journal of medical genetics. Part A 191 (4) (2023)
Sonja Neuser, Barbara Brechmann, Gali Heimer, Ines Brösse, Susanna Schubert, Lauren O'Grady, Michael Zech, Siddharth Srivastava, David A Sweetser, Yasemin Dincer, Volker Mall, Juliane Winkelmann, Christian Behrends, Basil T Darras, Robert J Graham, Parul Jayakar, Barry Byrne, Bat El Bar-Aluma, Yael Haberman, Amir Szeinberg, Hesham M Aldhalaan, Mais Hashem, Amal Al Tenaiji, Omar Ismayl, Asma E Al Nuaimi, Karima Maher, Shahnaz Ibrahim, Fatima Khan, Henry Houlden, Vijayalakshmi S Ramakumaran, Alistair T Pagnamenta, Jennifer E Posey, James R. Lupski, Wen-Hann Tan, Gehad ElGhazali, Isabella Herman, Tatiana Muñoz, Gabriela M Repetto, Angelika Seitz, Mandy Krumbiegel, Maria Cecilia Poli, Usha Kini, Stephanie Efthymiou, Jens Meiler, Reza Maroofian, Fowzan Sami Alkuraya, Rami Abou Jamra, Bernt Popp, Bruria Ben-Zeev, Darius Ebrahimi-Fakhari
Clinical, neuroimaging, and molecular spectrum of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disability. Human mutation 42 (6) (2021)
Mersedeh Rohanizadegan, Sarah Tracy, Carolina I Galarreta, Tabitha Poorvu, Terry L Buchmiller, Lynne M Bird, Judy A Estroff, Wen-Hann Tan
Genetic diagnoses and associated anomalies in fetuses prenatally diagnosed with esophageal atresia. American journal of medical genetics. Part A 182 (8) (2020)
Alissa M D'Gama, Eleina England, Jill A Madden, Jiahai Shi, Katherine R Chao, Monica Hsiung Wojcik, Alcy R Torres, Wen-Hann Tan, Gerard T Berry, Sanjay P Prabhu, Pankaj B Agrawal
Exome sequencing identifies novel missense and deletion variants in RTN4IP1 associated with optic atrophy, global developmental delay, epilepsy, ataxia, and choreoathetosis. American journal of medical genetics. Part A 185 (1) (2020)
Nasreen Khan, Raquel Cabo, Wen-Hann Tan, Regina Tayag, Lynne M Bird
Healthcare burden among individuals with Angelman syndrome: Findings from the Angelman Syndrome Natural History Study. Molecular genetics & genomic medicine 7 (7) (2019)
Anjali Sadhwani, Jennifer M Willen, Nicole LaVallee, Miganush Stepanians, Hillary Miller, Sarika U Peters, Rene L Barbieri-Welge, Lucia T Horowitz, Lisa M Noll, Rachel J Hundley, Lynne M Bird, Wen-Hann Tan
Maladaptive behaviors in individuals with Angelman syndrome. American journal of medical genetics. Part A 179 (6) (2019)
Anjali Sadhwani, J M Willen, H Miller, R Barbieri-Welge, L T Horowitz, L M Noll, S Peters, R Hundley, L M Bird, Wen-Hann Tan
Neurodevelopmental profile of siblings with Angelman syndrome due to pathogenic UBE3A variants. Journal of intellectual disability research : JIDR 64 (3) (2019)
Tova Hershkovitz, Alina Kurolap, Noa Ruhrman-Shahar, Daniel Monakier, Elizabeth T DeChene, Gabriela Peretz-Amit, Birgit Funke, Nili Zucker, Rafael Hirsch, Wen-Hann Tan, Hagit Baris Feldman
Clinical diversity of MYH7-related cardiomyopathies: Insights into genotype-phenotype correlations. American journal of medical genetics. Part A 179 (3) (2018)
Anjali Sadhwani, Neville E Sanjana, Jennifer M Willen, Stephen N Calculator, Emily D Black, Lora J H Bean, Hong Li, Wen-Hann Tan
Two Angelman families with unusually advanced neurodevelopment carry a start codon variant in the most highly expressed UBE3A isoform. American journal of medical genetics. Part A 176 (7) (2018)
Bo Hoon Lee, Margot R F Reijnders, Oluwatobi Abubakare, Emily Tuttle, Brynn Lape, Kelly Q Minks, Christopher Stodgell, Loisa Bennetto, Jennifer Kwon, Chin-To Fong, Karen W Gripp, Eric D Marsh, Wendy E Smith, Ahm M Huq, Stephanie A Coury, Wen-Hann Tan, Orestes Solis, Rupal I Mehta, Richard J Leventer, Diana Baralle, David Hunt, Alex R Paciorkowski
Expanding the neurodevelopmental phenotype of PURA syndrome. American journal of medical genetics. Part A 176 (1) (2017)
Wen-Hann Tan, Lynne M Bird, Anjali Sadhwani, Rene L Barbieri-Welge, Steven A Skinner, Lucia T Horowitz, Carlos A Bacino, Lisa M Noll, Cary Fu, Rachel J Hundley, Logan K Wink, Craig A Erickson, Gregory N Barnes, Anne M Slavotinek, Rita Jeremy, Alexander Rotenberg, Sanjeev V Kothare, Heather E Olson, Annapurna Poduri, Mark P Nespeca, Hillary C Chu, Jennifer M Willen, Kevin F Haas, Edwin J Weeber, Paul A Rufo
A randomized controlled trial of levodopa in patients with Angelman syndrome. American journal of medical genetics. Part A 176 (5) (2017)
Tara Wenger, Dong Li, Margaret H Harr, Wen-Hann Tan, Renata Pellegrino, Zornitza Stark, Hakon Hakonarson, Elizabeth Joyce Bhoj
Expanding the phenotypic spectrum of TP63-related disorders including the first set of monozygotic twins. American journal of medical genetics. Part A 176 (1) (2017)