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8 results for Cham,+Breana

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ArticlesPeer ReviewedFull Text
Germline AGO2 mutations impair RNA interference and human neurological development
Author / Creator:Lessel, Davor ; Zeitler, Daniela M. ; Reijnders, Margot R. F. ; Kazantsev, Andriy ; Hassani Nia, Fatemeh ; Bartholomäus, Alexander ; Martens, Victoria ; Bruckmann, Astrid ; Graus, Veronika ; McConkie-Rosell, Allyn ; McDonald, Marie ; Lozic, Bernarda ; Tan, Ee-Shien ; Gerkes, Erica ; Johannsen, Jessika ; Denecke, Jonas ; Telegrafi, Aida ; Zonneveld-Huijssoon, Evelien ; Lemmink, Henny H. ; Cham, Breana W. M. ; Kovacevic, Tanja ; Ramsdell, Linda ; Foss, Kimberly ; Le Duc, Diana ; Mitter, Diana ; Syrbe, Steffen ; Merkenschlager, Andreas ; Sinnema, Margje ; Panis, Bianca ; Lazier, Joanna ; Osmond, Matthew ; Hartley, Taila ; Mortreux, Jeremie ; Busa, Tiffany ; Missirian, Chantal ; Prasun, Pankaj ; Lüttgen, Sabine ; Mannucci, Ilaria ; Lessel, Ivana ; Schob, Claudia ; Kindler, Stefan ; Pappas, John ; Rabin, Rachel ; Willemsen, Marjolein ; Gardeitchik, Thatjana ; Löhner, Katharina ; Rump, Patrick ; Dias, Kerith-Rae ; Evans, Carey-Anne ; Andrews, Peter Ian ; Roscioli, Tony ; Brunner, Han G. ; Chijiwa, Chieko ; Lewis, M. E. Suzanne ; Jamra, Rami Abou ; Dyment, David A. ; Boycott, Kym M. ; Stegmann, Alexander P. A. ; Kubisch, Christian ; Tan, Ene-Choo ; Mirzaa, Ghayda M. ; McWalter, Kirsty ; Kleefstra, Tjitske ; Pfundt, Rolph ; Ignatova, Zoya ; Meister, Gunter ; Kreienkamp, Hans-Jürgen
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2020-11, Vol.11 (1), p.5797-14, Article 5797
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Massively parallel sequencing of patients with intellectual disability, congenital anomalies and/or autism spectrum disorders with a targeted gene panel
Author / Creator:Brett, Maggie ; McPherson, John ; Zang, Zhi Jiang ; Lai, Angeline ; Tan, Ee-Shien ; Ng, Ivy ; Ong, Lai-Choo ; Cham, Breana ; Tan, Patrick ; Rozen, Steve ; Tan, Ene-Choo
Publisher:United States: Public Library of Science
Journal title:PloS one, 2014-04, Vol.9 (4), p.e93409-e93409
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Genetic landscape of congenital disorders in patients from Southeast Asia: results from sequencing using a gene panel for Mendelian phenotypes
Author / Creator:Wei, Heming ; Lai, Angeline ; Tan, Ee Shien ; Koh, Mark Jean Aan ; Ng, Ivy ; Ting, Teck Wah ; Thomas, Terrence ; Cham, Breana ; Lim, Jiin Ying ; Kam, Sylvia ; Goh, Chew Yin Jasmine ; Lin, Grace ; Brett, Maggie ; Chan, Derrick ; Jamuar, Saumya Shekhar ; Tan, Ene-Choo
Publisher:England: BMJ Publishing Group LTD
Journal title:Archives of disease in childhood, 2021-01, Vol.106 (1), p.38-43
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Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management
Author / Creator:Bhatia, Neha S ; Lim, Jiin Ying ; Bonnard, Carine ; Kuan, Jyn-Ling ; Brett, Maggie ; Wei, Heming ; Cham, Breana ; Chin, Huilin ; Bosso-Lefevre, Celia ; Dharuman, Perumal ; Escande-Beillard, Nathalie ; Devasia, Arun George ; Goh, Chew Yin Jasmine ; Kam, Sylvia ; Liew, Wendy Kein-Meng ; Liew, Woei Kang ; Lin, Grace ; Jain, Kanika ; Ng, Alvin Yu-Jin ; Subramanian, Deepa ; Xie, Min ; Tan, Yuen-Ming ; Tawari, Nilesh R ; Tiang, Zenia ; Ting, Teck Wah ; Tohari, Sumanty ; Tong, Cheuk Ka ; Lezhava, Alexander ; Ng, Sarah B ; Law, Hai Yang ; Venkatesh, Byrappa ; Tomar, Swati ; Sethi, Raman ; Tan, Grace ; Shanmugasundaram, Arthi ; Goh, Denise Li-Meng ; Lai, Poh San ; Lai, Angeline ; Tan, Ee Shien ; Ng, Ivy ; Reversades, Bruno ; Tan, Ene Choo ; Foo, Roger ; Jamuar, Saumya Shekhar
Publisher:England: BMJ Publishing Group LTD
Journal title:Archives of disease in childhood, 2021-01, Vol.106 (1), p.31-37
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Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders
Author / Creator:Bylstra, Yasmin ; Kuan, Jyn Ling ; Lim, Weng Khong ; Bhalshankar, Jaydutt Digambar ; Teo, Jing Xian ; Davila, Sonia ; Te Teh, Bin an ; Rozen, Steve ; Tan, Ene-Choo ; Liew, Wendy Kein Meng ; Yeo, Khung Keong ; Tan, Patrick ; Saw, Seang Mei ; Cheng, Ching-Yu ; Cook, Stuart ; Foo, Roger ; Jamuar, Saumya Shekhar
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2019-01, Vol.21 (1), p.207-212
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A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia
Author / Creator:Laurino, Mercy Y. ; Leppig, Kathleen A. ; Abad, Peter James ; Cham, Breana ; Chu, Yoyo Wing Yiu ; Kejriwal, Saahil ; Lee, Juliana M. H. ; Sternen, Darci L. ; Thompson, Jennifer K. ; Burgess, Matthew J. ; Chien, Shu ; Elackatt, Niby ; Lim, Jiin Ying ; Sura, Thanyachai ; Faradz, Sultana ; Padilla, Carmencita ; Paz, Eva Cutiongco de-la ; Nauphar, Donny ; Nguyen, Khanh Ngoc ; Zayts, Olya ; Vu, Dung Chi ; Thong, Meow-Keong
Publisher:New York: Springer US
Journal title:Journal of genetic counseling, 2018-02, Vol.27 (1), p.21-32
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Left Ventricular Non-compaction: Is It Genetic?
Author / Creator:Ting, Teck Wah ; Jamuar, Saumya Shekhar ; Brett, Maggie Siewyan ; Tan, Ee Shien ; Cham, Breana Wen Min ; Lim, Jiin Ying ; Law, Hai Yang ; Tan, Ene Choo ; Choo, Jonathan Tze Liang ; Lai, Angeline Hwei Meeng
Publisher:New York: Springer US
Journal title:Pediatric cardiology, 2015-12, Vol.36 (8), p.1565-1572
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Massively Parallel Sequencing of Patients with Intellectual Disability, Congenital Anomalies and/or Autism Spectrum Disorders with a Targeted Gene Panel: e93409
Author / Creator:Brett, Maggie ; McPherson, John ; Zang, Zhi Jiang ; Lai, Angeline ; Tan, Ee-Shien ; Ng, Ivy ; Ong, Lai-Choo ; Cham, Breana ; Tan, Patrick ; Rozen, Steve
Journal title:PloS one, 2014-04, Vol.9 (4)
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Germline AGO2 mutations impair RNA interference and human neurological development

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Massively parallel sequencing of patients with intellectual disability, congenital anomalies and/or autism spectrum disorders with a targeted gene panel

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Genetic landscape of congenital disorders in patients from Southeast Asia: results from sequencing using a gene panel for Mendelian phenotypes

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Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management

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Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders

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A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia

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Left Ventricular Non-compaction: Is It Genetic?

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Massively Parallel Sequencing of Patients with Intellectual Disability, Congenital Anomalies and/or Autism Spectrum Disorders with a Targeted Gene Panel: e93409

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