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Author/Creator Tan, Wen‐Hann

1. A randomized controlled trial of levodopa in patients with Angelman syndrome. Issue 5 (25th September 2017)

Authors:
Tan, Wen‐Hann; Bird, Lynne M.; Sadhwani, Anjali; Barbieri‐Welge, Rene L.; Skinner, Steven A.; Horowitz, Lucia T.; Bacino, Carlos A.; Noll, Lisa M.; Fu, Cary; Hundley, Rachel J.; Wink, Logan K.; Erickson, Craig A.; Barnes, Gregory N.; Slavotinek, Anne; Jeremy, Rita; Rotenberg, Alexander; Kothare, ...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 5(2018)
Page Start:
1099
Record Type:
Journal Article
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4. Clinical diversity of MYH7‐related cardiomyopathies: Insights into genotype–phenotype correlations. Issue 3 (27th December 2018)

Authors:
Hershkovitz, Tova; Kurolap, Alina; Ruhrman‐Shahar, Noa; Monakier, Daniel; DeChene, Elizabeth T.; Peretz‐Amit, Gabriela; Funke, Birgit; Zucker, Nili; Hirsch, Rafael; Tan, Wen‐Hann; Baris Feldman, Hagit
Journal:
American journal of medical genetics
Issue:
Volume 179:Issue 3(2019)
Page Start:
365
Record Type:
Journal Article
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5. Clinical findings in 39 individuals with Bohring–Opitz syndrome from a global patient‐driven registry with implications for tumor surveillance and recurrence risk. Issue 4 (7th February 2023)

Authors:
Russell, Bianca E.; Kianmahd, Rebecca R.; Munster, Chelsea; Yu, Anna; Ahad, Leena; Tan, Wen‐Hann
Journal:
American journal of medical genetics
Issue:
Volume 191:Issue 4(2023)
Page Start:
1050
Record Type:
Journal Article
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6. Clinical management of patients with ASXL1 mutations and Bohring–Opitz syndrome, emphasizing the need for Wilms tumor surveillance. (29th April 2015)

Authors:
Russell, Bianca; Johnston, Jennifer J.; Biesecker, Leslie G.; Kramer, Nancy; Pickart, Angela; Rhead, William; Tan, Wen‐Hann; Brownstein, Catherine A.; Kate Clarkson, L.; Dobson, Amy; Rosenberg, Avi Z.; Vergano, Samantha A. Schrier; Helm, Benjamin M.; Harrison, Rachel E.; Graham, John M.
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 9(2015:Sep.)
Page Start:
2122
Record Type:
Journal Article
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7. Clinical, neuroimaging, and molecular spectrum of TECPR2‐associated hereditary sensory and autonomic neuropathy with intellectual disability. Issue 6 (11th May 2021)

Authors:
Neuser, Sonja; Brechmann, Barbara; Heimer, Gali; Brösse, Ines; Schubert, Susanna; O'Grady, Lauren; Zech, Michael; Srivastava, Siddharth; Sweetser, David A.; Dincer, Yasemin; Mall, Volker; Winkelmann, Juliane; Behrends, Christian; Darras, Basil T.; Graham, Robert J.; Jayakar, Parul; Byrne, Barry; ...
Journal:
Human mutation
Issue:
Volume 42:Issue 6(2021)
Page Start:
762
Record Type:
Journal Article
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8. Defining the phenotypic spectrum of SLC6A1 mutations. (8th January 2018)

Authors:
Johannesen, Katrine M.; Gardella, Elena; Linnankivi, Tarja; Courage, Carolina; de Saint Martin, Anne; Lehesjoki, Anna‐Elina; Mignot, Cyril; Afenjar, Alexandra; Lesca, Gaetan; Abi‐Warde, Marie‐Thérèse; Chelly, Jamel; Piton, Amélie; Merritt, J. Lawrence; Rodan, Lance H.; Tan, Wen‐Hann; Bird, Lynne ...
Journal:
Epilepsia
Issue:
Volume 59:issue 2(2018)
Page Start:
389
Record Type:
Journal Article
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9. Exome sequencing identifies novel missense and deletion variants in RTN4IP1 associated with optic atrophy, global developmental delay, epilepsy, ataxia, and choreoathetosis. Issue 1 (9th October 2020)

Authors:
D'Gama, Alissa M.; England, Eleina; Madden, Jill A.; Shi, Jiahai; Chao, Katherine R.; Wojcik, Monica H.; Torres, Alcy R.; Tan, Wen‐Hann; Berry, Gerard T.; Prabhu, Sanjay P.; Agrawal, Pankaj B.
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 1(2021)
Page Start:
203
Record Type:
Journal Article
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10. Expanding the neurodevelopmental phenotype of PURA syndrome. Issue 1 (17th November 2017)

Authors:
Lee, Bo Hoon; Reijnders, Margot R. F.; Abubakare, Oluwatobi; Tuttle, Emily; Lape, Brynn; Minks, Kelly Q.; Stodgell, Christopher; Bennetto, Loisa; Kwon, Jennifer; Fong, Chin‐To; Gripp, Karen W.; Marsh, Eric D.; Smith, Wendy E.; Huq, Ahm M.; Coury, Stephanie A.; Tan, Wen‐Hann; Solis, Orestes; Mehta...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 1(2018)
Page Start:
56
Record Type:
Journal Article
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