Engin Deniz (E Deniz)

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 17

Top Venues

Proceedings of the National Academy of Sciences of the United States of America

Life science alliance

Brain : a journal of neurology

Fluids and barriers of the CNS

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

Publications

Tyrone DeSpenza, Amrita Singh, Garrett Allington, Shujuan Zhao, Junghoon Lee, Emre Kiziltug, Mackenzi L Prina, Nicole Desmet, Huy Q Dang, Jennifer Fields, Carol Nelson-Williams, Junhui Zhang, Kedous Y Mekbib, Evan Dennis, Neel H Mehta, Phan Q Duy, Hermela Shimelis, Lauren K Walsh, Arnaud Marlier, Engin Deniz, Evelyn M R Lake, R Todd Constable, Ellen J Hoffman, Richard P Lifton, Allan T Gulledge, Steven N Fiering, Andres Moreno-De-Luca, Shozeb M Haider, Seth L Alper, Sheng Chih Jin, Kristopher T Kahle, Bryan W Luikart
Pathogenic variants in autism gene KATNAL2 cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics. Proceedings of the National Academy of Sciences of the United States of America 121 (27) (2024)
Tyrone DeSpenza, Amrita Singh, Garrett Allington, Shujuan Zhao, Junghoon Lee, Emre Kizlitug, Mackenzi L Prina, Nicole Desmet, Huy Q Dang, Jennifer Fields, Carol Nelson-Williams, Junhui Zhang, Kedous Y Mekbib, Evan Dennis, Neel H Mehta, Phan Q Duy, Hermela Shimelis, Lauren K Walsh, Arnaud Marlier, Engin Deniz, Evelyn M R Lake, R Todd Constable, Ellen J Hoffman, Richard P Lifton, Allan T Gulledge, Steven N Fiering, Andres Moreno-De-Luca, Shozeb M Haider, Seth L Alper, Sheng Chih Jin, Kristopher T Kahle, Bryan W Luikart
Pathogenic variants in autism gene KATNAL2 cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics. Proceedings of the National Academy of Sciences of the United States of America 121 (27) (2024)
Tyrone DeSpenza, Amrita Singh, Garrett Allington, Shujuan Zhao, Junghoon Lee, Emre Kiziltug, Mackenzi L Prina, Nicole Desmet, Huy Q Dang, Jennifer Fields, Carol Nelson-Williams, Junhui Zhang, Kedous Y Mekbib, Evan Dennis, Neel H Mehta, Phan Q Duy, Hermela Shimelis, Lauren K Walsh, Arnaud Marlier, Engin Deniz, Evelyn M R Lake, R Todd Constable, Ellen J Hoffman, Richard P Lifton, Allan T Gulledge, Steven N Fiering, Andres Moreno-De-Luca, Shozeb M Haider, Seth L Alper, Sheng Chih Jin, Kristopher T Kahle, Bryan W Luikart
Pathogenic variants in autism gene KATNAL2 cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics. Proceedings of the National Academy of Sciences of the United States of America 121 (27) (2024)
Angelina Haesoo Kim, Irmak Sakin, Stephen Viviano, Gulten Tuncel, Stephanie Marie Aguilera, Gizem Goles, Lauren Jeffries, Weizhen Ji, Saquib A Lakhani, Canan Ceylan Kose, Fatma Silan, Sukru Sadik Oner, Oktay Ismail Kaplan, null null, Mahmut Çerkez Ergoren, Ketu Mishra-Gorur, Murat Gunel, Sebnem Ozemri Sag, Sehime Gulsun Temel, Engin Deniz
CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. Life science alliance 7 (10) (2024)
Tyrone DeSpenza, Amrita Singh, Garrett Allington, Shujuan Zhao, Junghoon Lee, Emre Kiziltug, Mackenzi L Prina, Nicole Desmet, Huy Q Dang, Jennifer Fields, Carol Nelson-Williams, Junhui Zhang, Kedous Y Mekbib, Evan Dennis, Neel H Mehta, Phan Q Duy, Hermela Shimelis, Lauren K Walsh, Arnaud Marlier, Engin Deniz, Evelyn M R Lake, R Todd Constable, Ellen J Hoffman, Richard P Lifton, Allan T Gulledge, Steven N Fiering, Andres Moreno-De-Luca, Shozeb M Haider, Seth L Alper, Sheng Chih Jin, Kristopher T Kahle, Bryan W Luikart
Pathogenic variants in autism gene KATNAL2 cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics. Proceedings of the National Academy of Sciences of the United States of America 121 (27) (2024)
Amrita K Singh, Garrett Allington, Stephen Viviano, Stephen McGee, Emre Kiziltug, Shaojie Ma, Shujuan Zhao, Kedous Y Mekbib, John P Shohfi, Phan Q Duy, Tyrone DeSpenza, Charuta G Furey, Benjamin C Reeves, Hannah Smith, André M M Sousa, Adriana Cherskov, August Allocco, Carol Nelson-Williams, Shozeb M Haider, Syed R A Rizvi, Seth L Alper, Nenad Sestan, Hermela Shimelis, Lauren K Walsh, Richard P Lifton, Andres Moreno-De-Luca, Sheng Chih Jin, Paul Kruszka, Engin Deniz, Kristopher T Kahle
A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus. Brain : a journal of neurology 147 (4) (2024)
Ketu Mishra-Gorur, Tanyeri Barak, Leon D Kaulen, Octavian Henegariu, Sheng Chih Jin, Stephanie Marie Aguilera, Ezgi Yalbir, Gizem Goles, Sayoko Nishimura, Danielle Miyagishima, Lydia Djenoune, Selin Altinok, Devendra K Rai, Stephen Viviano, Andrew Prendergast, Cynthia Zerillo, Kent Ozcan, Burcin Baran, Leman Sencar, Nukte Goc, Yanki Yarman, A Gulhan Ercan-Encicek, Kaya Bilguvar, Richard P Lifton, Jennifer Moliterno, Angeliki Louvi, Shiaulou Yuan, Engin Deniz, Martina Brueckner, Murat Gunel
Reply to Pisan et al.: Pathogenicity of inherited TRAF7 mutations in congenital heart disease. Proceedings of the National Academy of Sciences of the United States of America 121 (12) (2024)
Amrita K Singh, Garrett Allington, Stephen Viviano, Stephen McGee, Emre Kiziltug, Shaojie Ma, Shujuan Zhao, Kedous Y Mekbib, John P Shohfi, Phan Q Duy, Tyrone DeSpenza, Charuta G Furey, Benjamin C Reeves, Hannah Smith, André M M Sousa, Adriana Cherskov, August Allocco, Carol Nelson-Williams, Shozeb M Haider, Syed R A Rizvi, Seth L Alper, Nenad Sestan, Hermela Shimelis, Lauren K Walsh, Richard P Lifton, Andres Moreno-De-Luca, Sheng Chih Jin, Paul Kruszka, Engin Deniz, Kristopher T Kahle
A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus. Brain : a journal of neurology 147 (4) (2024)
Tyrone DeSpenza, Amrita Singh, Garrett Allington, Shujuan Zhao, Junghoon Lee, Emre Kiziltug, Mackenzi L Prina, Nicole Desmet, Huy Q Dang, Jennifer Fields, Carol Nelson-Williams, Junhui Zhang, Kedous Y Mekbib, Evan Dennis, Neel H Mehta, Phan Q Duy, Hermela Shimelis, Lauren K Walsh, Arnaud Marlier, Engin Deniz, Evelyn M R Lake, R Todd Constable, Ellen J Hoffman, Richard P Lifton, Allan T Gulledge, Steven N Fiering, Andres Moreno-De-Luca, Shozeb M Haider, Seth L Alper, Sheng Chih Jin, Kristopher T Kahle, Bryan W Luikart
Pathogenic variants in autism gene KATNAL2 cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics. Proceedings of the National Academy of Sciences of the United States of America 121 (27) (2024)
Tyrone DeSpenza, Amrita Singh, Garrett Allington, Shujuan Zhao, Junghoon Lee, Emre Kiziltug, Mackenzi L Prina, Nicole Desmet, Huy Q Dang, Jennifer Fields, Carol Nelson-Williams, Junhui Zhang, Kedous Y Mekbib, Evan Dennis, Neel H Mehta, Phan Q Duy, Hermela Shimelis, Lauren K Walsh, Arnaud Marlier, Engin Deniz, Evelyn M R Lake, R Todd Constable, Ellen J Hoffman, Richard P Lifton, Allan T Gulledge, Steven N Fiering, Andres Moreno-De-Luca, Shozeb M Haider, Seth L Alper, Sheng Chih Jin, Kristopher T Kahle, Bryan W Luikart
Pathogenic variants in autism gene KATNAL2 cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics. Proceedings of the National Academy of Sciences of the United States of America 121 (27) (2024)
Ketu Mishra-Gorur, Tanyeri Barak, Leon D Kaulen, Octavian Henegariu, Sheng Chih Jin, Stephanie Marie Aguilera, Ezgi Yalbir, Gizem Goles, Sayoko Nishimura, Danielle Miyagishima, Lydia Djenoune, Selin Altinok, Devendra K Rai, Stephen Viviano, Andrew Prendergast, Cynthia Zerillo, Kent Ozcan, Burcin Baran, Leman Sencar, Nukte Goc, Yanki Yarman, A Gulhan Ercan-Encicek, Kaya Bilguvar, Richard P Lifton, Jennifer Moliterno, Angeliki Louvi, Shiaulou Yuan, Engin Deniz, Martina Brueckner, Murat Gunel
Reply to Pisan et al.: Pathogenicity of inherited TRAF7 mutations in congenital heart disease. Proceedings of the National Academy of Sciences of the United States of America 121 (12) (2024)
Tyrone DeSpenza, Amrita Singh, Garrett Allington, Shujuan Zhao, Junghoon Lee, Emre Kiziltug, Mackenzi L Prina, Nicole Desmet, Huy Q Dang, Jennifer Fields, Carol Nelson-Williams, Junhui Zhang, Kedous Y Mekbib, Evan Dennis, Neel H Mehta, Phan Q Duy, Hermela Shimelis, Lauren K Walsh, Arnaud Marlier, Engin Deniz, Evelyn M R Lake, R Todd Constable, Ellen J Hoffman, Richard P Lifton, Allan T Gulledge, Steven N Fiering, Andres Moreno-De-Luca, Shozeb M Haider, Seth L Alper, Sheng Chih Jin, Kristopher T Kahle, Bryan W Luikart
Pathogenic variants in autism gene KATNAL2 cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics. Proceedings of the National Academy of Sciences of the United States of America 121 (27) (2024)
Angelina Haesoo Kim, Irmak Sakin, Stephen Viviano, Gulten Tuncel, Stephanie Marie Aguilera, Gizem Goles, Lauren Jeffries, Weizhen Ji, Saquib A Lakhani, Canan Ceylan Kose, Fatma Silan, Sukru Sadik Oner, Oktay Ismail Kaplan, null null, Mahmut Çerkez Ergoren, Ketu Mishra-Gorur, Murat Gunel, Sebnem Ozemri Sag, Sehime Gulsun Temel, Engin Deniz
CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. Life science alliance 7 (10) (2024)
Angelina Haesoo Kim, Irmak Sakin, Stephen Viviano, Gulten Tuncel, Stephanie Marie Aguilera, Gizem Goles, Lauren Jeffries, Weizhen Ji, Saquib A Lakhani, Canan Ceylan Kose, Fatma Silan, Sukru Sadik Oner, Oktay Ismail Kaplan, null null, Mahmut Çerkez Ergoren, Ketu Mishra-Gorur, Murat Gunel, Sebnem Ozemri Sag, Sehime Gulsun Temel, Engin Deniz
CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. Life science alliance 7 (10) (2024)
Ketu Mishra-Gorur, Tanyeri Barak, Leon D Kaulen, Octavian Henegariu, Sheng Chih Jin, Stephanie Marie Aguilera, Ezgi Yalbir, Gizem Goles, Sayoko Nishimura, Danielle Miyagishima, Lydia Djenoune, Selin Altinok, Devendra K Rai, Stephen Viviano, Andrew Prendergast, Cynthia Zerillo, Kent Ozcan, Burcin Baran, Leman Sencar, Nukte Goc, Yanki Yarman, A Gulhan Ercan-Encicek, Kaya Bilguvar, Richard P Lifton, Jennifer Moliterno, Angeliki Louvi, Shiaulou Yuan, Engin Deniz, Martina Brueckner, Murat Gunel
Reply to Pisan et al.: Pathogenicity of inherited TRAF7 mutations in congenital heart disease. Proceedings of the National Academy of Sciences of the United States of America 121 (12) (2024)
Ketu Mishra-Gorur, Tanyeri Barak, Leon D Kaulen, Octavian Henegariu, Sheng Chih Jin, Stephanie Marie Aguilera, Ezgi Yalbir, Gizem Goles, Sayoko Nishimura, Danielle Miyagishima, Lydia Djenoune, Selin Altinok, Devendra K Rai, Stephen Viviano, Andrew Prendergast, Cynthia Zerillo, Kent Ozcan, Burcin Baran, Leman Sencar, Nukte Goc, Yanki Yarman, A Gulhan Ercan-Encicek, Kaya Bilguvar, Richard P Lifton, Jennifer Moliterno, Angeliki Louvi, Shiaulou Yuan, Engin Deniz, Martina Brueckner, Murat Gunel
Reply to Pisan et al.: Pathogenicity of inherited TRAF7 mutations in congenital heart disease. Proceedings of the National Academy of Sciences of the United States of America 121 (12) (2024)
A H Dur, T Tang, S Viviano, A Sekuri, H R Willsey, H D Tagare, K T Kahle, Engin Deniz
In Xenopus ependymal cilia drive embryonic CSF circulation and brain development independently of cardiac pulsatile forces. Fluids and barriers of the CNS 17 (1) (2020)

Engin Deniz.css-eqlu8i{font-size:small;padding-left:4px;} (E Deniz)

Publication Activity (10 Years)

Top Topics

Top Venues

Engin Deniz (E Deniz)