Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
Willsey, A. Jeremy, Sanders, Stephan J., Li, Mingfeng, Dong, Shan, Tebbenkamp, Andrew T., Muhle, Rebecca A., Reilly, Steven K., Lin, Leon, Fertuzinhos, Sofia, Miller, Jeremy A., Murtha, Michael T., Bichsel, Candace, Niu, Wei, Cotney, Justin, Ercan-Sencicek, A. Gulhan, Gockley, Jake, Gupta, Abha R., Han, Wenqi, He, Xin, Hoffman, Ellen J., Klei, Lambertus, Lei, Jing, Liu, Wenzhong, Liu, Li, Lu, Cong, Xu, Xuming, Zhu, Ying, Mane, Shrikant M., Lein, Ed S., Wei, Liping, Noonan, James P., Roeder, Kathryn, Devlin, Bernie, Sestan, Nenad, State, Matthew W.
Published in Cell (21.11.2013)
Published in Cell (21.11.2013)
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Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary Microcephaly
Li, Hongda, Bielas, Stephanie L., Zaki, Maha S., Ismail, Samira, Farfara, Dorit, Um, Kyongmi, Rosti, Rasim O., Scott, Eric C., Tu, Shu, Chi, Neil C., Gabriel, Stacey, Erson-Omay, Emine Z., Ercan-Sencicek, A. Gulhan, Yasuno, Katsuhito, Çağlayan, Ahmet Okay, Kaymakçalan, Hande, Ekici, Barış, Bilguvar, Kaya, Gunel, Murat, Gleeson, Joseph G.
Published in American journal of human genetics (04.08.2016)
Published in American journal of human genetics (04.08.2016)
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Novel compound heterozygous mutations in GPT2 linked to microcephaly, and intellectual developmental disability with or without spastic paraplegia
Kaymakcalan, Hande, Yarman, Yanki, Goc, Nukte, Toy, Fatih, Meral, Cihan, Ercan‐Sencicek, A. Gulhan, Gunel, Murat
Published in American journal of medical genetics. Part A (01.02.2018)
Published in American journal of medical genetics. Part A (01.02.2018)
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Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE
Celestino-Soper, Patricia B.S., Shaw, Chad A., Sanders, Stephan J., Li, Jian, Murtha, Michael T., Ercan-Sencicek, A. Gulhan, Davis, Lea, Thomson, Susanne, Gambin, Tomasz, Chinault, A. Craig, Ou, Zhishuo, German, Jennifer R., Milosavljevic, Aleksandar, Sutcliffe, James S., Cook, Edwin H., Stankiewicz, Pawel, State, Matthew W., Beaudet, Arthur L.
Published in Human molecular genetics (15.11.2011)
Published in Human molecular genetics (15.11.2011)
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Mutation spectrum of congenital heart disease in a consanguineous Turkish population
Dong, Weilai, Kaymakcalan, Hande, Jin, Sheng Chih, Diab, Nicholas S., Tanıdır, Cansaran, Yalcin, Ali Seyfi Yalim, Ercan‐Sencicek, A. Gulhan, Mane, Shrikant, Gunel, Murat, Lifton, Richard P., Bilguvar, Kaya, Brueckner, Martina
Published in Molecular genetics & genomic medicine (01.06.2022)
Published in Molecular genetics & genomic medicine (01.06.2022)
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Mutations in BCKD-kinase Lead to a Potentially Treatable Form of Autism with Epilepsy
Novarino, Gaia, El-Fishawy, Paul, Kayserili, Hulya, Meguid, Nagwa A., Scott, Eric M., Schroth, Jana, Silhavy, Jennifer L., Kara, Majdi, Khalil, Rehab O., Ben-Omran, Tawfeg, Ercan-Sencicek, A. Gulhan, Hashish, Adel F., Sanders, Stephan J., Gupta, Abha R., Hashem, Hebatalla S., Matern, Dietrich, Gabriel, Stacey, Sweetman, Larry, Rahimi, Yasmeen, Harris, Robert A., State, Matthew W., Gleeson, Joseph G.
Published in Science (American Association for the Advancement of Science) (19.10.2012)
Published in Science (American Association for the Advancement of Science) (19.10.2012)
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Engineering spatial-organized cardiac organoids for developmental toxicity testing
Hoang, Plansky, Kowalczewski, Andrew, Sun, Shiyang, Winston, Tackla S., Archilla, Adriana M., Lemus, Stephanie M., Ercan-Sencicek, A. Gulhan, Gupta, Abha R., Liu, Wenzhong, Kontaridis, Maria I., Amack, Jeffrey D., Ma, Zhen
Published in Stem cell reports (11.05.2021)
Published in Stem cell reports (11.05.2021)
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Rare Copy Number Variants in Tourette Syndrome Disrupt Genes in Histaminergic Pathways and Overlap with Autism
Fernandez, Thomas V, Sanders, Stephan J, Yurkiewicz, Ilana R, Ercan-Sencicek, A. Gulhan, Kim, Young-Shin, Fishman, Daniel O, Raubeson, Melanie J, Song, Youeun, Yasuno, Katsuhito, Ho, Winson S.C, Bilguvar, Kaya, Glessner, Joseph, Chu, Su Hee, Leckman, James F, King, Robert A, Gilbert, Donald L, Heiman, Gary A, Tischfield, Jay A, Hoekstra, Pieter J, Devlin, Bernie, Hakonarson, Hakon, Mane, Shrikant M, Günel, Murat, State, Matthew W
Published in Biological psychiatry (1969) (01.03.2012)
Published in Biological psychiatry (1969) (01.03.2012)
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De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder
Dong, Shan, Walker, Michael F, Carriero, Nicholas J, DiCola, Michael, Willsey, A Jeremy, Ye, Adam Y, Waqar, Zainulabedin, Gonzalez, Luis E, Overton, John D, Frahm, Stephanie, Keaney, 3rd, John F, Teran, Nicole A, Dea, Jeanselle, Mandell, Jeffrey D, Hus Bal, Vanessa, Sullivan, Catherine A, DiLullo, Nicholas M, Khalil, Rehab O, Gockley, Jake, Yuksel, Zafer, Sertel, Sinem M, Ercan-Sencicek, A Gulhan, Gupta, Abha R, Mane, Shrikant M, Sheldon, Michael, Brooks, Andrew I, Roeder, Kathryn, Devlin, Bernie, State, Matthew W, Wei, Liping, Sanders, Stephan J
Published in Cell reports (Cambridge) (09.10.2014)
Published in Cell reports (Cambridge) (09.10.2014)
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Searching for Potocki–Lupski syndrome phenotype: A patient with language impairment and no autism
Gulhan Ercan-Sencicek, A, Davis Wright, Nicole R, Frost, Stephen J, Fulbright, Robert K, Felsenfeld, Susan, Hart, Lesley, Landi, Nicole, Einar Mencl, W, Sanders, Stephan J, Pugh, Kenneth R, State, Matthew W, Grigorenko, Elena L
Published in Brain & development (Tokyo. 1979) (01.09.2012)
Published in Brain & development (Tokyo. 1979) (01.09.2012)
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Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans
Ercan-Sencicek, A Gulhan, Jambi, Samira, Franjic, Daniel, Nishimura, Sayoko, Li, Mingfeng, El-Fishawy, Paul, Morgan, Thomas M, Sanders, Stephan J, Bilguvar, Kaya, Suri, Mohnish, Johnson, Michele H, Gupta, Abha R, Yuksel, Zafer, Mane, Shrikant, Grigorenko, Elena, Picciotto, Marina, Alberts, Arthur S, Gunel, Murat, Šestan, Nenad, State, Matthew W
Published in European journal of human genetics : EJHG (01.02.2015)
Published in European journal of human genetics : EJHG (01.02.2015)
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Neurogenetic analysis of childhood disintegrative disorder
Gupta, Abha R, Westphal, Alexander, Yang, Daniel Y J, Sullivan, Catherine A W, Eilbott, Jeffrey, Zaidi, Samir, Voos, Avery, Vander Wyk, Brent C, Ventola, Pam, Waqar, Zainulabedin, Fernandez, Thomas V, Ercan-Sencicek, A Gulhan, Walker, Michael F, Choi, Murim, Schneider, Allison, Hedderly, Tammy, Baird, Gillian, Friedman, Hannah, Cordeaux, Cara, Ristow, Alexandra, Shic, Frederick, Volkmar, Fred R, Pelphrey, Kevin A
Published in Molecular autism (04.04.2017)
Published in Molecular autism (04.04.2017)
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Histidine Decarboxylase Deficiency Causes Tourette Syndrome: Parallel Findings in Humans and Mice
Castellan Baldan, Lissandra, Williams, Kyle A., Gallezot, Jean-Dominique, Pogorelov, Vladimir, Rapanelli, Maximiliano, Crowley, Michael, Anderson, George M., Loring, Erin, Gorczyca, Roxanne, Billingslea, Eileen, Wasylink, Suzanne, Panza, Kaitlyn E., Ercan-Sencicek, A. Gulhan, Krusong, Kuakarun, Leventhal, Bennett L., Ohtsu, Hiroshi, Bloch, Michael H., Hughes, Zoë A., Krystal, John H., Mayes, Linda, de Araujo, Ivan, Ding, Yu-Shin, State, Matthew W., Pittenger, Christopher
Published in Neuron (Cambridge, Mass.) (04.06.2014)
Published in Neuron (Cambridge, Mass.) (04.06.2014)
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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Sanders, Stephan J., He, Xin, Willsey, A. Jeremy, Ercan-Sencicek, A. Gulhan, Samocha, Kaitlin E., Cicek, A. Ercument, Murtha, Michael T., Bal, Vanessa H., Bishop, Somer L., Dong, Shan, Goldberg, Arthur P., Jinlu, Cai, Keaney, John F., Klei, Lambertus, Mandell, Jeffrey D., Moreno-De-Luca, Daniel, Poultney, Christopher S., Robinson, Elise B., Smith, Louw, Solli-Nowlan, Tor, Su, Mack Y., Teran, Nicole A., Walker, Michael F., Werling, Donna M., Beaudet, Arthur L., Cantor, Rita M., Fombonne, Eric, Geschwind, Daniel H., Grice, Dorothy E., Lord, Catherine, Lowe, Jennifer K., Mane, Shrikant M., Martin, Donna M., Morrow, Eric M., Talkowski, Michael E., Sutcliffe, James S., Walsh, Christopher A., Yu, Timothy W., Ledbetter, David H., Martin, Christa Lese, Cook, Edwin H., Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, State, Matthew W.
Published in Neuron (Cambridge, Mass.) (23.09.2015)
Published in Neuron (Cambridge, Mass.) (23.09.2015)
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De novo mutations revealed by whole-exome sequencing are strongly associated with autism
SANDERS, Stephan J, MURTHA, Michael T, WALKER, Michael F, OBER, Gordon T, TERAN, Nicole A, SONG, Youeun, EL-FISHAWY, Paul, MURTHA, Ryan C, CHOI, Murim, OVERTON, John D, BJORNSON, Robert D, CARRIERO, Nicholas J, GUPTA, Abha R, MEYER, Kyle A, BILGUVAR, Kaya, MANE, Shrikant M, SESTAN, Nenad, LIFTON, Richard P, GIINEL, Murat, ROEDER, Kathryn, GESCHWIND, Daniel H, DEVNN, Bernie, STATE, Matthew W, MURDOCH, John D, RAUBESON, Melanie J, WILLSEY, A. Jeremy, ERCAN-SENCICEK, A. Gulhan, DILULLO, Nicholas M, PARIKSHAK, Neelroop N, STEIN, Jason L
Published in Nature (London) (10.05.2012)
Published in Nature (London) (10.05.2012)
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Journal Article
Histidine decarboxylase deficiency causes tourette syndrome: parallel findings in humans and mice
Baldan, Lissandra Castellan, Williams, Kyle A, Gallezot, Jean-Dominique, Pogorelov, Vladimir, Rapanelli, Maximiliano, Crowley, Michael, Anderson, George M, Loring, Erin, Gorczyca, Roxanne, Billingslea, Eileen, Wasylink, Suzanne, Panza, Kaitlyn E, Ercan-Sencicek, A Gulhan, Krusong, Kuakarun, Leventhal, Bennett L, Ohtsu, Hiroshi, Bloch, Michael H, Hughes, Zoë A, Krystal, John H, Mayes, Linda, de Araujo, Ivan, Ding, Yu-Shin, State, Matthew W, Pittenger, Christopher
Published in Neuron (Cambridge, Mass.) (08.01.2014)
Published in Neuron (Cambridge, Mass.) (08.01.2014)
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Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease
Mishra-Gorur, Ketu, Barak, Tanyeri, Kaulen, Leon D, Henegariu, Octavian, Jin, Sheng Chih, Aguilera, Stephanie Marie, Yalbir, Ezgi, Goles, Gizem, Nishimura, Sayoko, Miyagishima, Danielle, Djenoune, Lydia, Altinok, Selin, Rai, Devendra K, Viviano, Stephen, Prendergast, Andrew, Zerillo, Cynthia, Ozcan, Kent, Baran, Burcin, Sencar, Leman, Goc, Nukte, Yarman, Yanki, Ercan-Sencicek, A Gulhan, Bilguvar, Kaya, Lifton, Richard P, Moliterno, Jennifer, Louvi, Angeliki, Yuan, Shiaulou, Deniz, Engin, Brueckner, Martina, Gunel, Murat
Published in Proceedings of the National Academy of Sciences - PNAS (18.04.2023)
Published in Proceedings of the National Academy of Sciences - PNAS (18.04.2023)
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