Mustafa Sahin (Mustafa Şahin, M Sahin)

Loop profile Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 104

Top Venues

Annals of clinical and translational neurology

Nature communications

Journal of neurodevelopmental disorders

Journal of inherited metabolic disease

Children's Hospital Boston

Yale University School of Medicine (PHD)

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

Affiliation History

Children's Hospital Boston Mar 01 2016

United States

Professor :: Neurology

Education History

Yale University School of Medicine

United States

PHD

Publications

Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Afshin Saffari, Barbara Brechmann, Cedric Böger, Wardiya Afshar Saber, Hellen Jumo, Dosh Whye, Delaney Wood, Lara Wahlster, Julian E Alecu, Marvin Ziegler, Marlene Scheffold, Kellen Winden, Jed Hubbs, Elizabeth D Buttermore, Lee Barrett, Georg H H Borner, Alexandra K Davies, Darius Ebrahimi-Fakhari, Mustafa Sahin
High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegia. Nature communications 15 (1) (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Andrew Dhawan, Sarah Baitamouni, Darren Liu, Robyn M Busch, Patricia Klaas, Thomas W Frazier, Siddharth Srivastava, Sumit Parikh, Gary E Hsich, Neil R Friedman, David M Ritter, Antonio Y Hardan, Julian A Martinez, Mustafa Sahin, Charis Eng
Exploring the neurological features of individuals with germline PTEN variants: A multicenter study. Annals of clinical and translational neurology 11 (5) (2024)
Mary Bronwen L Chalkley, Lindsey N Guerin, Tenhir Iyer, Samantha Mallahan, Sydney Nelson, Mustafa Sahin, Emily Hodges, Kevin C Ess, Rebecca A Ihrie
Human TSC2 Mutant Cells Exhibit Aberrations in Early Neurodevelopment Accompanied by Changes in the DNA Methylome. bioRxiv : the preprint server for biology (2024)
James E Dowling, Terry Pirovolakis, Keshini Devakandan, Ana Stosic, Mia Pidsadny, Elisa Nigro, Mustafa Sahin, Darius Ebrahimi-Fakhari, Souad Messahel, Ganapathy Varadarajan, Benjamin M Greenberg, Xin Chen, Berge A Minassian, Ronald D Cohn, Carsten G Bonnemann, Steven J Gray
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient. Nature medicine 30 (7) (2024)
Vasiliki Karalis, Delaney Wood, Nicole A Teaney, Mustafa Sahin
The role of TSC1 and TSC2 proteins in neuronal axons. Molecular psychiatry 29 (4) (2024)
Andrew Dhawan, Sarah Baitamouni, Darren Liu, Robyn M Busch, Patricia Klaas, Thomas W Frazier, Siddharth Srivastava, Sumit Parikh, Gary E Hsich, Neil R Friedman, David M Ritter, Antonio Y Hardan, Julian A Martinez, Mustafa Sahin, Charis Eng
Exploring the neurological features of individuals with germline PTEN variants: A multicenter study. Annals of clinical and translational neurology 11 (5) (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Mary Bronwen L Chalkley, Lindsey N Guerin, Tenhir Iyer, Samantha Mallahan, Sydney Nelson, Mustafa Sahin, Emily Hodges, Kevin C Ess, Rebecca A Ihrie
Human TSC2 Mutant Cells Exhibit Aberrations in Early Neurodevelopment Accompanied by Changes in the DNA Methylome. bioRxiv : the preprint server for biology (2024)
Afshin Saffari, Barbara Brechmann, Cedric Böger, Wardiya Afshar Saber, Hellen Jumo, Dosh Whye, Delaney Wood, Lara Wahlster, Julian E Alecu, Marvin Ziegler, Marlene Scheffold, Kellen Winden, Jed Hubbs, Elizabeth D Buttermore, Lee Barrett, Georg H H Borner, Alexandra K Davies, Darius Ebrahimi-Fakhari, Mustafa Sahin
High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegia. Nature communications 15 (1) (2024)
James E Dowling, Terry Pirovolakis, Keshini Devakandan, Ana Stosic, Mia Pidsadny, Elisa Nigro, Mustafa Sahin, Darius Ebrahimi-Fakhari, Souad Messahel, Ganapathy Varadarajan, Benjamin M Greenberg, Xin Chen, Berge A Minassian, Ronald D Cohn, Carsten G Bonnemann, Steven J Gray
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient. Nature medicine 30 (7) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
James E Dowling, Terry Pirovolakis, Keshini Devakandan, Ana Stosic, Mia Pidsadny, Elisa Nigro, Mustafa Sahin, Darius Ebrahimi-Fakhari, Souad Messahel, Ganapathy Varadarajan, Benjamin M Greenberg, Xin Chen, Berge A Minassian, Ronald D Cohn, Carsten G Bonnemann, Steven J Gray
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient. Nature medicine 30 (7) (2024)
Afshin Saffari, Barbara Brechmann, Cedric Böger, Wardiya Afshar Saber, Hellen Jumo, Dosh Whye, Delaney Wood, Lara Wahlster, Julian E Alecu, Marvin Ziegler, Marlene Scheffold, Kellen Winden, Jed Hubbs, Elizabeth D Buttermore, Lee Barrett, Georg H H Borner, Alexandra K Davies, Darius Ebrahimi-Fakhari, Mustafa Sahin
High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegia. Nature communications 15 (1) (2024)
Siddharth Srivastava, Fanghan Yang, Anna K Prohl, Peter E Davis, Jamie K Capal, Rajna Filip-Dhima, E Martina Bebin, Darcy A Krueger, Hope Northrup, Joyce Y Wu, Simon K Warfield, Mustafa Sahin, Bo Zhang, null null
Abnormality of Early White Matter Development in Tuberous Sclerosis Complex and Autism Spectrum Disorder: Longitudinal Analysis of Diffusion Tensor Imaging Measures. Journal of child neurology 39 (5-6) (2024)
Siddharth Srivastava, Fanghan Yang, Anna K Prohl, Peter E Davis, Jamie K Capal, Rajna Filip-Dhima, E Martina Bebin, Darcy A Krueger, Hope Northrup, Joyce Y Wu, Simon K Warfield, Mustafa Sahin, Bo Zhang, null null
Abnormality of Early White Matter Development in Tuberous Sclerosis Complex and Autism Spectrum Disorder: Longitudinal Analysis of Diffusion Tensor Imaging Measures. Journal of child neurology (2024)
Vasiliki Karalis, Delaney Wood, Nicole A Teaney, Mustafa Sahin
The role of TSC1 and TSC2 proteins in neuronal axons. Molecular psychiatry 29 (4) (2024)
Vasiliki Karalis, Delaney Wood, Nicole A Teaney, Mustafa Sahin
The role of TSC1 and TSC2 proteins in neuronal axons. Molecular psychiatry (2024)
Andrew Dhawan, Sarah Baitamouni, Darren Liu, Robyn M Busch, Patricia Klaas, Thomas W Frazier, Siddharth Srivastava, Sumit Parikh, Gary E Hsich, Neil R Friedman, David M Ritter, Antonio Y Hardan, Julian A Martinez, Mustafa Sahin, Charis Eng
Exploring the neurological features of individuals with germline PTEN variants: A multicenter study. Annals of clinical and translational neurology 11 (5) (2024)
James E Dowling, Terry Pirovolakis, Keshini Devakandan, Ana Stosic, Mia Pidsadny, Elisa Nigro, Mustafa Sahin, Darius Ebrahimi-Fakhari, Souad Messahel, Ganapathy Varadarajan, Benjamin M Greenberg, Xin Chen, Berge A Minassian, Ronald D Cohn, Carsten G Bonnemann, Steven J Gray
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient. Nature medicine 30 (7) (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Afshin Saffari, Barbara Brechmann, Cedric Böger, Wardiya Afshar Saber, Hellen Jumo, Dosh Whye, Delaney Wood, Lara Wahlster, Julian E Alecu, Marvin Ziegler, Marlene Scheffold, Kellen Winden, Jed Hubbs, Elizabeth D Buttermore, Lee Barrett, Georg H H Borner, Alexandra K Davies, Darius Ebrahimi-Fakhari, Mustafa Sahin
High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegia. Nature communications 15 (1) (2024)
Mary Bronwen L Chalkley, Lindsey N Guerin, Tenhir Iyer, Samantha Mallahan, Sydney Nelson, Mustafa Sahin, Emily Hodges, Kevin C Ess, Rebecca A Ihrie
Human TSC2 Mutant Cells Exhibit Aberrations in Early Neurodevelopment Accompanied by Changes in the DNA Methylome. bioRxiv : the preprint server for biology (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Siddharth Srivastava, Fanghan Yang, Anna K Prohl, Peter E Davis, Jamie K Capal, Rajna Filip-Dhima, E Martina Bebin, Darcy A Krueger, Hope Northrup, Joyce Y Wu, Simon K Warfield, Mustafa Sahin, Bo Zhang, null null
Abnormality of Early White Matter Development in Tuberous Sclerosis Complex and Autism Spectrum Disorder: Longitudinal Analysis of Diffusion Tensor Imaging Measures. Journal of child neurology 39 (5-6) (2024)
Afshin Saffari, Barbara Brechmann, Cedric Böger, Wardiya Afshar Saber, Hellen Jumo, Dosh Whye, Delaney Wood, Lara Wahlster, Julian E Alecu, Marvin Ziegler, Marlene Scheffold, Kellen Winden, Jed Hubbs, Elizabeth D Buttermore, Lee Barrett, Georg H H Borner, Alexandra K Davies, Darius Ebrahimi-Fakhari, Mustafa Sahin
High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegia. Nature communications 15 (1) (2024)
Andrew Dhawan, Sarah Baitamouni, Darren Liu, Robyn M Busch, Patricia Klaas, Thomas W Frazier, Siddharth Srivastava, Sumit Parikh, Gary E Hsich, Neil R Friedman, David M Ritter, Antonio Y Hardan, Julian A Martinez, Mustafa Sahin, Charis Eng
Exploring the neurological features of individuals with germline PTEN variants: A multicenter study. Annals of clinical and translational neurology 11 (5) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Afshin Saffari, Barbara Brechmann, Cedric Böger, Wardiya Afshar Saber, Hellen Jumo, Dosh Whye, Delaney Wood, Lara Wahlster, Julian E Alecu, Marvin Ziegler, Marlene Scheffold, Kellen Winden, Jed Hubbs, Elizabeth D Buttermore, Lee Barrett, Georg H H Borner, Alexandra K Davies, Darius Ebrahimi-Fakhari, Mustafa Sahin
High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegia. Nature communications 15 (1) (2024)
Andrew Dhawan, Sarah Baitamouni, Darren Liu, Robyn M Busch, Patricia Klaas, Thomas W Frazier, Siddharth Srivastava, Sumit Parikh, Gary E Hsich, Neil R Friedman, David M Ritter, Antonio Y Hardan, Julian A Martinez, Mustafa Sahin, Charis Eng
Exploring the neurological features of individuals with germline PTEN variants: A multicenter study. Annals of clinical and translational neurology 11 (5) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Margaret C Savage, Geraldine Bliss, Joseph D Buxbaum, Jordan S Farrell, April R Levin, Siddharth Srivastava, Elizabeth Berry-Kravis, J Lloyd Holder, Mustafa Sahin
A roadmap for SHANK3-related Epilepsy Research: recommendations from the 2023 strategic planning workshop. Therapeutic advances in rare disease 5 (2024)
Afshin Saffari, Barbara Brechmann, Cedric Böger, Wardiya Afshar Saber, Hellen Jumo, Dosh Whye, Delaney Wood, Lara Wahlster, Julian E Alecu, Marvin Ziegler, Marlene Scheffold, Kellen Winden, Jed Hubbs, Elizabeth D Buttermore, Lee Barrett, Georg H H Borner, Alexandra K Davies, Darius Ebrahimi-Fakhari, Mustafa Sahin
High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegia. Nature communications 15 (1) (2024)
Andrew Dhawan, Sarah Baitamouni, Darren Liu, Robyn M Busch, Patricia Klaas, Thomas W Frazier, Siddharth Srivastava, Sumit Parikh, Gary E Hsich, Neil R Friedman, David M Ritter, Antonio Y Hardan, Julian A Martinez, Mustafa Sahin, Charis Eng
Exploring the neurological features of individuals with germline PTEN variants: A multicenter study. Annals of clinical and translational neurology 11 (5) (2024)
Andrew Dhawan, Sarah Baitamouni, Darren Liu, Robyn M Busch, Patricia Klaas, Thomas W Frazier, Siddharth Srivastava, Sumit Parikh, Gary E Hsich, Neil R Friedman, David M Ritter, Antonio Y Hardan, Julian A Martinez, Mustafa Sahin, Charis Eng
Exploring the neurological features of individuals with germline PTEN variants: A multicenter study. Annals of clinical and translational neurology (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease (2024)
James E Dowling, Terry Pirovolakis, Keshini Devakandan, Ana Stosic, Mia Pidsadny, Elisa Nigro, Mustafa Sahin, Darius Ebrahimi-Fakhari, Souad Messahel, Ganapathy Varadarajan, Benjamin M Greenberg, Xin Chen, Berge A Minassian, Ronald D Cohn, Carsten G Bonnemann, Steven J Gray
AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient. Nature medicine (2024)
Siddharth Srivastava, Fanghan Yang, Anna K Prohl, Peter E Davis, Jamie K Capal, Rajna Filip-Dhima, E Martina Bebin, Darcy A Krueger, Hope Northrup, Joyce Y Wu, Simon K Warfield, Mustafa Sahin, Bo Zhang, null null
Abnormality of Early White Matter Development in Tuberous Sclerosis Complex and Autism Spectrum Disorder: Longitudinal Analysis of Diffusion Tensor Imaging Measures. Journal of child neurology 39 (5-6) (2024)
Jacquelyn A Brown, Shannon L Faley, Monika Judge, Patricia Ward, Rebecca A Ihrie, Robert Carson, Laura Armstrong, Mustafa Sahin, John P Wikswo, Kevin C Ess, M Diana Neely
Rescue of Impaired Blood-Brain Barrier in Tuberous Sclerosis Complex Patient Derived Neurovascular Unit. bioRxiv : the preprint server for biology (2023)
Janelle Applequist, Cristina M Burroughs, Peter A Merkel, Xiaoting Chen, Bruce C Trapnell, Robert J Desnick, Mustafa Sahin, Jeffrey P Krischer
Direct-to-Consumer Recruitment Methods via Traditional and Social Media to Aid in Research Accrual for Clinical Trials for Rare Diseases: Comparative Analysis Study. Journal of medical Internet research 25 (2023)
Janelle Applequist, Cristina M Burroughs, Peter A Merkel, Xiaoting Chen, Bruce C Trapnell, Robert J Desnick, Mustafa Sahin, Jeffrey P Krischer
Direct-to-Consumer Recruitment Methods via Traditional and Social Media to Aid in Research Accrual for Clinical Trials for Rare Diseases: Comparative Analysis Study. Journal of medical Internet research 25 (2023)
Jacquelyn A Brown, Shannon L Faley, Monika Judge, Patricia Ward, Rebecca A Ihrie, Robert Carson, Laura Armstrong, Mustafa Sahin, John P Wikswo, Kevin C Ess, M Diana Neely
Rescue of Impaired Blood-Brain Barrier in Tuberous Sclerosis Complex Patient Derived Neurovascular Unit. bioRxiv : the preprint server for biology (2023)
Sameer C Dhamne, Meera E Modi, Audrey Gray, Simone Bonazzi, Lucas Craig, Elizabeth Bainbridge, Lahin Lalani, Chloe E Super, Samantha Schaeffer, Ketthsy Capre, Danuta Lubicka, Guiqing Liang, Doug Burdette, Stephanie M McTighe, Sarika Gurnani, Sheryl Anne D Vermudez, Daniel Curtis, Christopher J Wilson, Mustafa Q Hameed, Angelica D'Amore, Alexander Rotenberg, Mustafa Sahin
Seizure reduction in TSC2-mutant mouse model by an mTOR catalytic inhibitor. Annals of clinical and translational neurology (2023)
Janelle Applequist, Cristina M Burroughs, Peter A Merkel, Xiaoting Chen, Bruce C Trapnell, Robert J Desnick, Mustafa Sahin, Jeffrey P Krischer
Direct-to-Consumer Recruitment Methods via Traditional and Social Media to Aid in Research Accrual for Clinical Trials for Rare Diseases: Comparative Analysis Study. Journal of medical Internet research 25 (2023)
Jacquelyn A Brown, Shannon L Faley, Monika Judge, Patricia Ward, Rebecca A Ihrie, Robert Carson, Laura Armstrong, Mustafa Sahin, John P Wikswo, Kevin C Ess, M Diana Neely
Rescue of Impaired Blood-Brain Barrier in Tuberous Sclerosis Complex Patient Derived Neurovascular Unit. bioRxiv : the preprint server for biology (2023)
Jacquelyn A Brown, Shannon L Faley, Monika Judge, Patricia Ward, Rebecca A Ihrie, Robert Carson, Laura Armstrong, Mustafa Sahin, John P Wikswo, Kevin C Ess, M Diana Neely
Rescue of Impaired Blood-Brain Barrier in Tuberous Sclerosis Complex Patient Derived Neurovascular Unit. bioRxiv : the preprint server for biology (2023)
Mary-Bronwen L Chalkley, Rachel B Mersfelder, Maria Sundberg, Laura C Armstrong, Mustafa Sahin, Rebecca A Ihrie, Kevin C Ess
Non-canonical functions of a mutant TSC2 protein in mitotic division. PloS one 18 (10) (2023)
Afshin Saffari, Barbara Brechmann, Cedric Boeger, Wardiya Afshar Saber, Hellen Jumo, Dosh Whye, Delaney Wood, Lara Wahlster, Julian Alecu, Marvin Ziegler, Marlene Scheffold, Kellen Winden, Jed Hubbs, Elizabeth D Buttermore, Lee Barrett, Georg H H Borner, Alexandra K Davies, Mustafa Sahin, Darius Ebrahimi-Fakhari
High-Content Small Molecule Screen Identifies a Novel Compound That Restores AP-4-Dependent Protein Trafficking in Neuronal Models of AP-4-Associated Hereditary Spastic Paraplegia. Research square (2023)
E Martina Bebin, Jurriaan M Peters, Brenda E Porter, Tarrant O McPherson, Sarah O'Kelley, Mustafa Sahin, Katherine S Taub, Rajsekar Rajaraman, Stephanie C Randle, William M McClintock, Mary Kay Koenig, Mike D Frost, Hope A Northrup, Klaus Werner, Danielle A Nolan, Michael Wong, Jessica L Krefting, Fred Biasini, Kalyani Peri, Gary Cutter, Darcy A Krueger, null null
Early Treatment with Vigabatrin Does Not Decrease Focal Seizures or Improve Cognition in Tuberous Sclerosis Complex: The PREVeNT Trial. Annals of neurology (2023)
Petrus J de Vries, Tosca-Marie Heunis, Stephanie Vanclooster, Nola J Chambers, Stacey Bissell, Anna W Byars, Jennifer Flinn, Tanjala T Gipson, Agnies M van Eeghen, Robert Waltereit, Jamie K Capal, Sebastián Cukier, Peter E Davis, Catherine Smith, J Chris Kingswood, Eva Schoeters, Shoba Srivastava, Megumi Takei, Sugnet Gardner-Lubbe, Aubrey J Kumm, Darcy A Krueger, Mustafa Sahin, Liesbeth De Waele, Anna C Jansen
International consensus recommendations for the identification and treatment of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND). Journal of neurodevelopmental disorders 15 (1) (2023)
Stephanie Vanclooster, Stacey Bissell, Agnies M van Eeghen, Nola Chambers, Liesbeth De Waele, Anna W Byars, Jamie K Capal, Sebastián Cukier, Peter E Davis, Jennifer Flinn, Sugnet Gardner-Lubbe, Tanjala Gipson, Tosca-Marie Heunis, Dena Hook, J Christopher Kingswood, Darcy A Krueger, Aubrey J Kumm, Mustafa Sahin, Eva Schoeters, Catherine Smith, Shoba Srivastava, Megumi Takei, Robert Waltereit, Anna C Jansen, Petrus J de Vries
The research landscape of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND)-a comprehensive scoping review. Journal of neurodevelopmental disorders 14 (1) (2022)
Francisco J Garcia, Na Sun, Hyeseung Lee, Brianna Godlewski, Hansruedi Mathys, Kyriaki Galani, Blake Zhou, Xueqiao Jiang, Ayesha P Ng, Julio Mantero, Li-Huei Tsai, David A Bennett, Mustafa Sahin, Manolis Kellis, Myriam Heiman
Single-cell dissection of the human brain vasculature. Nature 603 (7903) (2022)
Alexander Li Cohen, Mallory R Kroeck, Juliana Wall, Peter McManus, Arina Ovchinnikova, Mustafa Sahin, Darcy A Krueger, E Martina Bebin, Hope Northrup, Joyce Y Wu, Simon K Warfield, Jurriaan M Peters, Michael D Fox, null null
Tubers Affecting the Fusiform Face Area Are Associated with Autism Diagnosis. Annals of neurology (2022)
Julian Emanuel Alecu, Afshin Saffari, Hellen Jumo, Marvin Ziegler, Oleksandr Strelko, Catherine A Brownstein, Joseph Gonzalez-Heydrich, Lance H Rodan, Mark P Gorman, Mustafa Sahin, Darius Ebrahimi-Fakhari
Novel CAPN1 missense variants in complex hereditary spastic paraplegia with early-onset psychosis. Annals of clinical and translational neurology 9 (4) (2022)
Maya Chopra, Dustin L Gable, Jamie Love-Nichols, Alexa Tsao, Shira Rockowitz, Piotr Sliz, Elizabeth Barkoudah, Lucia Bastianelli, David Coulter, Emily Davidson, Claudio M De Gusmao, David Fogelman, Kathleen Huth, Paige Marshall, Donna Nimec, Jessica Solomon Sanders, Benjamin J Shore, Brian Snyder, Scellig S D Stone, Ana Ubeda, Colyn Watkins, Charles Berde, Jeffrey Bolton, Catherine Brownstein, Michael Costigan, Darius Ebrahimi-Fakhari, Abbe Lai, Anne O'Donnell-Luria, Alex R Paciorkowski, Anna Pinto, John Pugh, Lance Rodan, Eugene Roe, Lindsay Swanson, Bo Zhang, Michael C Kruer, Mustafa Sahin, Annapurna H Poduri, Siddharth Srivastava
Mendelian etiologies identified with whole exome sequencing in cerebral palsy. Annals of clinical and translational neurology 9 (2) (2022)
Afshin Saffari, Melanie Kellner, Catherine Jordan, Helena Rosengarten, Alisa Mo, Bo Zhang, Oleksandr Strelko, Sonja Neuser, Marie Y Davis, Nobuaki Yoshikura, Naonobu Futamura, Tomoya Takeuchi, Shin Nabatame, Hiroyuki Ishiura, Shoji Tsuji, Huda Shujaa Aldeen, Elisa Cali, Clarissa Rocca, Henry Houlden, Stephanie Efthymiou, null null, Birgit Assmann, Grace Yoon, Bianca A Trombetta, Pia Kivisäkk, Florian S Eichler, Haitian Nan, Yoshihisa Takiyama, Alessandra Tessa, Filippo Maria Santorelli, Mustafa Sahin, C Shan Xu, Edward Yang, Rebecca Schüle, Darius Ebrahimi-Fakhari
The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15. Brain : a journal of neurology (2022)
Alexandra K Davies, Julian Emanuel Alecu, Marvin Ziegler, Catherine G Vasilopoulou, Fabrizio Merciai, Hellen Jumo, Wardiya Afshar Saber, Mustafa Sahin, Darius Ebrahimi-Fakhari, Georg H H Borner
AP-4-mediated axonal transport controls endocannabinoid production in neurons. Nature communications 13 (1) (2022)
Siddharth Srivastava, Booil Jo, Bo Zhang, Thomas Frazier, Anne Snow Gallagher, Fleming Peck, April R Levin, Sangeeta Mondal, Zetan Li, Rajna Filip-Dhima, Gregory Geisel, Kira A Dies, Amelia Diplock, Charis Eng, Rabi Hanna, Mustafa Sahin, Antonio Hardan, null null
A randomized controlled trial of everolimus for neurocognitive symptoms in PTEN hamartoma tumor syndrome. Human molecular genetics 31 (20) (2022)
Jasbir Singh Dalal, Kellen Diamond Winden, Catherine Lourdes Salussolia, Maria Sundberg, Achint Singh, Truc Thanh Pham, Pingzhu Zhou, William T Pu, Meghan T Miller, Mustafa Sahin
Loss of Tsc1 in cerebellar Purkinje cells induces transcriptional and translation changes in FMRP target transcripts. eLife 10 (2021)
Darius Ebrahimi-Fakhari, Julian Emanuel Alecu, Marvin Ziegler, Gregory Geisel, Catherine Jordan, Angelica D'Amore, Rebecca C Yeh, Shyam K Akula, Afshin Saffari, Sanjay P Prabhu, Mustafa Sahin, Edward Yang, null null
Systematic Analysis of Brain MRI Findings in Adaptor Protein Complex 4-Associated Hereditary Spastic Paraplegia. Neurology 97 (19) (2021)
Alexander Li Cohen, Brechtje P F Mulder, Anna K Prohl, Louis Soussand, Peter Davis, Mallory R Kroeck, Peter McManus, Ali Gholipour, Benoit Scherrer, E Martina Bebin, Joyce Y Wu, Hope Northrup, Darcy A Krueger, Mustafa Sahin, Simon K Warfield, Michael D Fox, Jurriaan M Peters, null null
Tuber Locations Associated with Infantile Spasms Map to a Common Brain Network. Annals of neurology 89 (4) (2021)
Lan Huang, Colette Bichsel, Alexis Norris, Jeremy Thorpe, Jonathan Pevsner, Sanda Alexandrescu, Anna Pinto, David Zurakowski, Robin J Kleiman, Mustafa Sahin, Arin K Greene, Joyce Bischoff
Endothelial GNAQ p.R183Q Increases ANGPT2 (Angiopoietin-2) and Drives Formation of Enlarged Blood Vessels. Arteriosclerosis, thrombosis, and vascular biology (2021)
Tess Levy, Jennifer H Foss-Feig, Catalina Betancur, Paige M Siper, Maria Pilar Trelles-Thorne, Danielle Halpern, Yitzchak Frank, Reymundo Lozano, Christina Layton, Bari Britvan, Jonathan A Bernstein, Joseph D Buxbaum, Elizabeth Berry-Kravis, Craig M Powell, Siddharth Srivastava, Mustafa Sahin, Latha Soorya, Audrey Thurm, Alexander Kolevzon, null null
Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: Results from the developmental Synaptopathies consortium. Human molecular genetics (2021)
Thomas W Frazier, Ritika Jaini, Robyn M Busch, Matthew Wolf, Tammy Sadler, Patricia Klaas, Antonio Y Hardan, Julian A Martinez, Mustafa Sahin, Charis Eng, null null
Cross-level analysis of molecular and neurobehavioral function in a prospective series of patients with germline heterozygous PTEN mutations with and without autism. Molecular autism 12 (1) (2021)
Maria Sundberg, Hannah Pinson, Richard S Smith, Kellen D Winden, Pooja Venugopal, Derek J C Tai, James F Gusella, Michael E Talkowski, Christopher A Walsh, Max Tegmark, Mustafa Sahin
16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro. Nature communications 12 (1) (2021)
Jamie K Capal, Marian E Williams, Deborah A Pearson, Robin Kissinger, Paul S Horn, Donna Murray, Kristn Currans, Bridget Kent, Martina Bebin, Hope Northrup, Joyce Y Wu, Mustafa Sahin, Darcy A Krueger, null null
Profile of Autism Spectrum Disorder in Tuberous Sclerosis Complex: Results from a Longitudinal, Prospective, Multisite Study. Annals of neurology 90 (6) (2021)
Christopher J Yuskaitis, Leigh-Ana Rossitto, Karenna J Groff, Sameer C Dhamne, Bo Zhang, Lahin K Lalani, Achint K Singh, Alexander Rotenberg, Mustafa Sahin
Factors influencing the acute pentylenetetrazole-induced seizure paradigm and a literature review. Annals of clinical and translational neurology 8 (7) (2021)
Livia O Loureiro, Jennifer L Howe, Miriam S Reuter, Alana Iaboni, Kristina Calli, Delnaz Roshandel, Iva Pritišanac, Alan Moses, Julie D Forman-Kay, Brett Trost, Mehdi Zarrei, Olivia Rennie, Lynette Y S Lau, Christian R Marshall, Siddharth Srivastava, Brianna Godlewski, Elizabeth D Buttermore, Mustafa Sahin, Dean Hartley, Thomas Frazier, Jacob A S Vorstman, Stelios Georgiades, Suzanne M E Lewis, Peter Szatmari, Clarrisa A Lisa Bradley, Anne-Claude Tabet, Marjolaine Willems, Serge Lumbroso, Amélie Piton, James Lespinasse, Richard Delorme, Thomas Bourgeron, Evdokia Anagnostou, Stephen W Scherer
A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder. NPJ genomic medicine 6 (1) (2021)
J O R Hernandez, X Wang, M Vazquez-Segoviano, Marta Lopez-Marfil, M F Sobral-Reyes, A Moran-Horowich, Maria Sundberg, D O Lopez-Cantu, C K Probst, G U Ruiz-Esparza, K Giannikou, R Abdi, E P Henske, David J Kwiatkowski, Mustafa Sahin, Dario R Lemos
A tissue-bioengineering strategy for modeling rare human kidney diseases in vivo. Nature communications 12 (1) (2021)
Darius Ebrahimi-Fakhari, Julian E Alecu, Barbara Brechmann, Marvin Ziegler, Kathrin Eberhardt, Hellen Jumo, Angelica D'Amore, Parham Habibzadeh, Mohammad Ali Faghihi, Jan L De Bleecker, Sandrine Vuillaumier-Barrot, Stėphane Auvin, Filippo M Santorelli, Sonja Neuser, Bernt Popp, Edward Yang, Lee Barrett, Alexandra K Davies, Afshin Saffari, Jennifer Hirst, Mustafa Sahin
High-throughput imaging of ATG9A distribution as a diagnostic functional assay for adaptor protein complex 4-associated hereditary spastic paraplegia. Brain communications 3 (4) (2021)
Angelica D'Amore, Alessandra Tessa, Valentina Naef, Maria Teresa Bassi, Andrea Citterio, Romina Romaniello, Gianluca Fichi, Daniele Galatolo, Serena Mero, Roberta Battini, Giulia Bertocci, Jacopo Baldacci, Federico Sicca, Federica Gemignani, Ivana Ricca, Anna Rubegni, Jennifer Hirst, Maria Marchese, Mustafa Sahin, Darius Ebrahimi-Fakhari, Filippo Maria Santorelli
Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52. Annals of clinical and translational neurology 7 (4) (2020)
Inês do Carmo G Gonçalves, Johanna Brecht, Maximilian Paul Thelen, Wiebke A Rehorst, Miriam Peters, Hyun Ju Lee, Susanne Motameny, Laura Torres-Benito, Darius Ebrahimi-Fakhari, Natalia L Kononenko, Janine Altmüller, David Vilchez, Mustafa Sahin, Brunhilde Wirth, Min Jeong Kye
Author Correction: Neuronal activity regulates DROSHA via autophagy in spinal muscular atrophy. Scientific reports 10 (1) (2020)
Krinio Giannikou, Zachary Zhu, Jaegil Kim, Kellen D Winden, Magdalena E Tyburczy, David Marron, Joel S Parker, Zachary T Herbert, Anika Bongaarts, Len Taing, Henry W Long, William V Pisano, Sanda Alexandrescu, Brianna Godlewski, Mark Nellist, Katarzyna Kotulska, Sergiusz Jozwiak, Marcin Roszkowski, Marek Mandera, Elizabeth A Thiele, Hart Lidov, Gad Getz, Orrin Devinsky, Michael S Lawrence, Keith L Ligon, David W Ellison, Mustafa Sahin, Eleonora Aronica, David M Meredith, David J Kwiatkowski
Subependymal giant cell astrocytomas are characterized by mTORC1 hyperactivation, a very low somatic mutation rate, and a unique gene expression profile. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 34 (2) (2020)
Marian E Williams, Deborah A Pearson, Jamie K Capal, Anna W Byars, Donna S Murray, Robin Kissinger, Sarah E O'Kelley, Ellen Hanson, Nicole M Bing, Bridget Kent, Joyce Y Wu, Hope Northrup, E Martina Bebin, Mustafa Sahin, Darcy Krueger, null null
Impacting development in infants with tuberous sclerosis complex: Multidisciplinary research collaboration. The American psychologist 74 (3) (2020)
Ian A Cook, Andrew C Wilson, Jurriaan M Peters, Monisha N Goyal, E Martina Bebin, Hope Northrup, Darcy A Krueger, Andrew F Leuchter, Mustafa Sahin, null null
EEG Spectral Features in Sleep of Autism Spectrum Disorders in Children with Tuberous Sclerosis Complex. Journal of autism and developmental disorders 50 (3) (2020)
Wardiya Afshar Saber, Mustafa Sahin
Recent advances in human stem cell-based modeling of Tuberous Sclerosis Complex. Molecular autism 11 (1) (2020)
Sanem Pinar Uysal, Mustafa Sahin
Tuberous sclerosis: a review of the past, present, and future Turkish journal of medical sciences 50 (SI-2) (2020)
Anne-Elise C de Groen, Jeffrey Bolton, Ann Marie Bergin, Mustafa Sahin, Jurriaan M Peters
The Evolution of Subclinical Seizures in Children With Tuberous Sclerosis Complex. Journal of child neurology 34 (12) (2019)
Jurriaan M Peters, Robbert R Struyven, Anna K Prohl, Lana Vasung, Andrija Stajduhar, Maxime Taquet, John J Bushman, Hart Lidov, Jolene M Singh, Benoit Scherrer, Joseph R Madsen, Sanjay P Prabhu, Mustafa Sahin, Onur Afacan, Simon K Warfield
White matter mean diffusivity correlates with myelination in tuberous sclerosis complex. Annals of clinical and translational neurology 6 (7) (2019)
Kellen Diamond Winden, Maria Sundberg, Cindy Yang, Syed Mohammad Adil Wafa, Sean Dwyer, Pin-Fang Chen, Elizabeth D Buttermore, Mustafa Sahin
Biallelic Mutations in TSC2 Lead to Abnormalities Associated with Cortical Tubers in Human iPSC-Derived Neurons. The Journal of neuroscience : the official journal of the Society for Neuroscience 39 (47) (2019)
Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, David H Ledbetter, Christa L Martin, Wendy K Chung, Helen V Firth, Thomas Frazier, Robin L Hansen, Lisa Prock, Han Brunner, Ny Hoang, Stephen W Scherer, Mustafa Sahin, David T Miller, null null
Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)
Krinio Giannikou, Kathryn D Lasseter, Joannes M Grevelink, Magdalena E Tyburczy, Kira A Dies, Zachary Zhu, Lana Hamieh, Bruce M Wollison, Aaron R Thorner, Stephen J Ruoss, Elizabeth A Thiele, Mustafa Sahin, David J Kwiatkowski
Low-level mosaicism in tuberous sclerosis complex: prevalence, clinical features, and risk of disease transmission. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)
Robyn M Busch, Siddharth Srivastava, Olivia Hogue, Thomas W Frazier, Patricia Klaas, Antonio Hardan, Julian A Martinez-Agosto, Mustafa Sahin, Charis Eng, null null
Neurobehavioral phenotype of autism spectrum disorder associated with germline heterozygous mutations in PTEN. Translational psychiatry 9 (1) (2019)
Stephan J Sanders, Mustafa Sahin, Joseph Hostyk, Audrey Thurm, Sebastien Jacquemont, Paul Avillach, Elise Douard, Christa L Martin, Meera E Modi, Andrés Moreno De Luca, Armin Raznahan, Alan Anticevic, Ricardo Dolmetsch, Guoping Feng, Daniel H Geschwind, David C Glahn, David B Goldstein, David H Ledbetter, Jennifer G Mulle, Sergiu P Pașca, Rodney C Samaco, Jonathan Sebat, Anne Pariser, Thomas Lehner, Raquel E Gur, Carrie E Bearden
A framework for the investigation of rare genetic disorders in neuropsychiatry. Nature medicine 25 (10) (2019)
Inês do Carmo G Gonçalves, Johanna Brecht, Maximilian Paul Thelen, Wiebke A Rehorst, Miriam Peters, Hyun Ju Lee, Susanne Motameny, Laura Torres-Benito, Darius Ebrahimi-Fakhari, Natalia L Kononenko, Janine Altmüller, David Vilchez, Mustafa Sahin, Brunhilde Wirth, Min Jeong Kye
Author Correction: Neuronal activity regulates DROSHA via autophagy in spinal muscular atrophy. Scientific reports 8 (1) (2018)
Heather M O'Leary, Walter E Kaufmann, Katherine V Barnes, Kshitiz Rakesh, Kush Kapur, Daniel C Tarquinio, Nicole G Cantwell, Katherine J Roche, Suzanne A Rose, Alexandra C Walco, Natalie M Bruck, Grace A Bazin, Ingrid A Holm, Mark E Alexander, Lindsay C Swanson, Lauren M Baczewski, Chi‐Sang Poon, Juan M Mayor Torres, Charles A Nelson, Mustafa Sahin
Placebo-controlled crossover assessment of mecasermin for the treatment of Rett syndrome. Annals of clinical and translational neurology 5 (3) (2018)
Emma A van der Poest Clement, Mustafa Sahin, Jurriaan M Peters
Vigabatrin for Epileptic Spasms and Tonic Seizures in Tuberous Sclerosis Complex. Journal of child neurology 33 (8) (2018)
Inês do Carmo G Gonçalves, Johanna Brecht, Maximilian Paul Thelen, Wiebke A Rehorst, Miriam Peters, Hyun Ju Lee, Susanne Motameny, Laura Torres-Benito, Darius Ebrahimi-Fakhari, Natalia L Kononenko, Janine Altmüller, David Vilchez, Mustafa Sahin, Brunhilde Wirth, Min Jeong Kye
Neuronal activity regulates DROSHA via autophagy in spinal muscular atrophy. Scientific reports 8 (1) (2018)
Meera E Modi, Mustafa Sahin
The Way Forward for Mechanism-Based Therapeutics in Genetically Defined Neurodevelopmental Disorders. Clinical pharmacology and therapeutics 104 (4) (2018)
Maria Sundberg, Ivan Tochitsky, David E Buchholz, Kellen Winden, Ville Kujala, Kush Kapur, Deniz Cataltepe, Daria Turner, Min-Joon Han, Clifford J Woolf, Mary E Hatten, Mustafa Sahin
Purkinje cells derived from TSC patients display hypoexcitability and synaptic deficits associated with reduced FMRP levels and reversed by rapamycin. Molecular psychiatry 23 (11) (2018)
Kristina Jülich, Ilana Neuberger, Mustafa Sahin, Masanori Takeoka, Anna Pinto, Sanjay P Prabhu
Yield of Emergent Neuroimaging in Patients With Sturge-Weber Syndrome Presenting With Acute Neurologic Symptoms. Journal of child neurology 34 (1) (2018)
Darcy A Krueger, Anjali Sadhwani, Anna W Byars, Petrus J de Vries, David N Franz, Vicky H Whittemore, Rajna Filip-Dhima, Donna Murray, Kush Kapur, Mustafa Sahin
Everolimus for treatment of tuberous sclerosis complex-associated neuropsychiatric disorders. Annals of clinical and translational neurology 4 (12) (2017)
Ebru Ercan, Juliette M Han, Alessia Di Nardo, Kellen Winden, Min-Joon Han, Leonie Hoyo, Afshin Saffari, Andrew Leask, Daniel H Geschwind, Mustafa Sahin
Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex. The Journal of experimental medicine 214 (3) (2017)
Siddharth Srivastava, Mustafa Sahin
Autism spectrum disorder and epileptic encephalopathy: common causes, many questions. Journal of neurodevelopmental disorders 9 (2017)
Elyza Kelly, Samantha M Schaeffer, Sameer C Dhamne, Jonathan O Lipton, Lothar Lindemann, Michael Honer, Georg Jaeschke, Chloe E Super, Stephen Ht Lammers, Meera E Modi, Jill L Silverman, John R Dreier, David J Kwiatkowski, Alexander Rotenberg, Mustafa Sahin
mGluR5 Modulation of Behavioral and Epileptic Phenotypes in a Mouse Model of Tuberous Sclerosis Complex. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 43 (6) (2017)
Sameer C Dhamne, Jill L Silverman, Chloe E Super, Stephen H T Lammers, Mustafa Q Hameed, Meera E Modi, Nycole A Copping, Michael C Pride, Daniel G Smith, Alexander Rotenberg, Jacqueline N Crawley, Mustafa Sahin
Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism. Molecular autism 8 (2017)

Mustafa Sahin.css-eqlu8i{font-size:small;padding-left:4px;} (Mustafa Şahin, M Sahin)

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Mustafa Sahin (Mustafa Şahin, M Sahin)