All papers authored by Stephanie Bielas
Refreshing results…
Stephanie Bielas 
,
Charles Ryan,
Samantha Regan,
Yao-Chang Tsan,
Eleanor Mills,
Emily Gong,
Yi-Ting Lai,
Jason Sheingold,
Khushboo Patel,
Theodore Horowitz,
Amanda Moccia,
Anshika Srivast
Upload
,
Charles Ryan,
Samantha Regan,
Yao-Chang Tsan,
Eleanor Mills,
Emily Gong,
Yi-Ting Lai,
Jason Sheingold,
Khushboo Patel,
Theodore Horowitz,
Amanda Moccia,
Anshika Srivast
Upload
2022
Enrica Boda ,
Martina Lorenzati ,
Roberta Parolisi ,
Brian Harding,
Gianmarco Pallavicini ,
Luca Bonfanti ,
Amanda Moccia ,
Stephanie Bielas ,
Ferdinando Di Cunto ,
Annalisa Buffo
Download from www.nature.com
,
Martina Lorenzati ,
Roberta Parolisi ,
Brian Harding,
Gianmarco Pallavicini ,
Luca Bonfanti ,
Amanda Moccia ,
Stephanie Bielas ,
Ferdinando Di Cunto ,
Annalisa Buffo
Download from www.nature.com
Anshika Srivastava,
Brian McGrath,
Stephanie L. Bielas
Histone H2A Monoubiquitination in Neurodevelopmental Disorders
Upload
Rasim Ozgur Rosti,
Bethany N. Sotak,
Stephanie L. Bielas ,
Gifty Bhat,
Jennifer L. Silhavy,
Ayca Dilruba Aslanger,
Umut Altunoglu,
Ilmay Bilge,
Mehmet Tasdemir,
Amanda D. Yzaguirrem,
Damir Musaev,
Sofia Infante,
Whitney Thuong,
Isaac Marin-Valencia,
Stanley F. Nelson
and 2 other authors
Upload
,
Gifty Bhat,
Jennifer L. Silhavy,
Ayca Dilruba Aslanger,
Umut Altunoglu,
Ilmay Bilge,
Mehmet Tasdemir,
Amanda D. Yzaguirrem,
Damir Musaev,
Sofia Infante,
Whitney Thuong,
Isaac Marin-Valencia,
Stanley F. Nelson
and 2 other authors
Upload
R. Kc,
A. Srivastava,
J. M. Wilkowski,
C. E. Richter,
J. A. Shavit,
D. T. Burke,
S. L. Bielas
Detection of nucleotide-specific CRISPR/Cas9 modified alleles using multiplex ligation detection
Download from www.nature.com
Malavika Hebbar,
Harsha Prasada L.,
Aneek Das Bhowmik,
Daniel Trujillano,
Anju Shukla,
Shrijeet Chakraborti,
Krishna Kumar Kandaswamy,
Arndt Rolfs,
Nutan Kamath,
Ashwin Dalal,
Stephanie Bielas ,
Katta Mohan Girisha
,
Katta Mohan Girisha
Homozygous deletion of exons 2 and 3 of NPC2 associated with Niemann-Pick disease type C
Download from api.wiley.com
Brian N. Harding,
Amanda Moccia,
Séverine Drunat,
Omar Soukarieh,
Hélène Tubeuf,
Lyn S. Chitty ,
Alain Verloes,
Pierre Gressens,
Vincent El Ghouzzi,
Sylvie Joriot,
Ferdinando Di Cunto,
Alexandra Martins,
Sandrine Passemard,
Stephanie L. Bielas
,
Alain Verloes,
Pierre Gressens,
Vincent El Ghouzzi,
Sylvie Joriot,
Ferdinando Di Cunto,
Alexandra Martins,
Sandrine Passemard,
Stephanie L. Bielas
Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons
Download from doi.org
Hongda Li,
Stephanie L. Bielas ,
Maha S. Zaki,
Samira Ismail,
Dorit Farfara,
Kyongmi Um,
Rasim O. Rosti,
Eric C. Scott,
Shu Tu,
Neil C. Chi,
Stacey Gabriel,
Emine Z. Erson-Omay,
A. Gulhan Ercan-Sencicek,
Katsuhito Yasuno,
Ahmet Okay Çağlayan
and 5 other authors
,
Maha S. Zaki,
Samira Ismail,
Dorit Farfara,
Kyongmi Um,
Rasim O. Rosti,
Eric C. Scott,
Shu Tu,
Neil C. Chi,
Stacey Gabriel,
Emine Z. Erson-Omay,
A. Gulhan Ercan-Sencicek,
Katsuhito Yasuno,
Ahmet Okay Çağlayan
and 5 other authors
Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary Microcephaly
Download from doi.org
2015
Anshika Srivastava,
K. C. Ritesh,
Yao-Chang Tsan,
Rosy Liao,
Fengyun Su,
Xuhong Cao,
Mark C. Hannibal,
Catherine E. Keegan,
Arul M. Chinnaiyan,
Donna M. Martin,
Stephanie L. Bielas
Download from europepmc.org
Download from europepmc.org
2014
Seung Tae Baek ,
Geraldine Kerjan,
Stephanie L. Bielas ,
Ji Eun Lee,
Ali G. Fenstermaker,
Gaia Novarino,
G. Gaia Novarino,
Joseph G. Gleeson
Download from www.ncbi.nlm.nih.gov
,
Geraldine Kerjan,
Stephanie L. Bielas ,
Ji Eun Lee,
Ali G. Fenstermaker,
Gaia Novarino,
G. Gaia Novarino,
Joseph G. Gleeson
Download from www.ncbi.nlm.nih.gov
2012
Tracy J. Dixon-Salazar,
Jennifer L. Silhavy,
Nitin Udpa,
Jana Schroth,
Stephanie Bielas ,
Ashleigh E. Schaffer,
Jesus Olvera,
Vineet Bafna,
Maha S. Zaki,
Ghada H. Abdel Salam,
Ghada H. Abdel-Salam,
Lobna A. Mansour,
Laila Selim,
Sawsan Abdel-Hadi,
Naima Marzouki
and 16 other authors
,
Ashleigh E. Schaffer,
Jesus Olvera,
Vineet Bafna,
Maha S. Zaki,
Ghada H. Abdel Salam,
Ghada H. Abdel-Salam,
Lobna A. Mansour,
Laila Selim,
Sawsan Abdel-Hadi,
Naima Marzouki
and 16 other authors
Exome Sequencing Can Improve Diagnosis and Alter Patient Management
Download from www.ncbi.nlm.nih.govMissing publications? Search for publications with a matching author name.