Both proliferation and lipogenesis of brown adipocytes contribute to postnatal brown adipose tissue growth in mice

بواسطة Negron, Steven G., Ercan-Sencicek, A. Gulhan, Freed, Jessica, Walters, Madeline, Lin, Zhiqiang
الحاوية / القاعدة Sci Rep (2020)

High levels of histamine decarboxylase in the striatum of mice and rats

بواسطة Krusong, Kuakarun, Ercan-Sencicek, A. Gulhan, Xu, Meiyu, Ohtsu, Hiroshi, Anderson, George M., State, Matthew W., Pittenger, Christopher
منشور في 2011

A balanced t(10;15) translocation in a male patient with developmental language disorder

بواسطة Ercan-Sencicek, A. Gulhan, Davis Wright, Nicole R., Sanders, Stephan J., Oakman, Nicole, Valdes, Lianna, Bakkaloglu, Betul, Doyle, Niamh, Yrigollen, Carolyn M., Morgan, Thomas M., Grigorenko, Elena L.
منشور في 2011

Engineering spatial-organized cardiac organoids for developmental toxicity testing

بواسطة 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
الحاوية / القاعدة Stem Cell Reports (2021)

Searching for Potocki-Lupski syndrome Phenotype: A Patient with Language Impairment and no Autism

بواسطة Ercan-Sencicek, A. Gulhan, Wright, Nicole R. Davis, Frost, Stephen J., Fulbright, Robert K., Felsenfeld, Susan, Hart, Lesley, Landi, Nicole, Mencl, W. Einar, Sanders, Stephan J., Pugh, Kenneth R., State, Matthew W., Grigorenko, Elena L.
منشور في 2011

Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE

بواسطة 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.
منشور في 2011

Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans

بواسطة 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
الحاوية / القاعدة Eur J Hum Genet (2015)

Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders

بواسطة Bakkaloglu, Betul, O'Roak, Brian J., Louvi, Angeliki, Gupta, Abha R., Abelson, Jesse F., Morgan, Thomas M., Chawarska, Katarzyna, Klin, Ami, Ercan-Sencicek, A. Gulhan, Stillman, Althea A., Tanriover, Gamze, Abrahams, Brett S., Duvall, Jackie A., Robbins, Elissa M., Geschwind, Daniel H., Biederer, Thomas, Gunel, Murat, Lifton, Richard P., State, Matthew W.
منشور في 2008

Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary Microcephaly

بواسطة 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.
الحاوية / القاعدة Am J Hum Genet (2016)

Mutations in BCKD-kinase Lead to a Potentially Treatable Form of Autism with Epilepsy

بواسطة 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.
منشور في 2012

Neurogenetic analysis of childhood disintegrative disorder

بواسطة 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.
الحاوية / القاعدة Mol Autism (2017)

Histidine decarboxylase deficiency causes Tourette syndrome: parallel findings in humans and mice

بواسطة 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
منشور في 2014

Rare Copy Number Variants in Tourette Syndrome Disrupt Genes in Histaminergic Pathways and Overlap with Autism

بواسطة 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 SC, 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
منشور في 2011

Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas

بواسطة Clark, Victoria E, Harmancı, Akdes Serin, Bai, Hanwen, Youngblood, Mark W, Lee, Tong Ihn, Baranoski, Jacob F, Ercan-Sencicek, A Gulhan, Abraham, Brian J, Weintraub, Abraham S, Hnisz, Denes, Simon, Matthias, Krischek, Boris, Erson-Omay, E Zeynep, Henegariu, Octavian, Carrión-Grant, Geneive, Mishra-Gorur, Ketu, Durán, Daniel, Goldmann, Johanna E, Schramm, Johannes, Goldbrunner, Roland, Piepmeier, Joseph M, Vortmeyer, Alexander O, Günel, Jennifer Moliterno, Bilgüvar, Kaya, Yasuno, Katsuhito, Young, Richard A, Günel, Murat
الحاوية / القاعدة Nat Genet (2016)

l-Histidine Decarboxylase and Tourette's Syndrome

بواسطة Ercan-Sencicek, A. Gulhan, Stillman, Althea A., Ghosh, Ananda K., Bilguvar, Kaya, O'Roak, Brian J., Mason, Christopher E., Abbott, Thomas, Gupta, Abha, King, Robert A., Pauls, David L., Tischfield, Jay A., Heiman, Gary A., Singer, Harvey S., Gilbert, Donald L., Hoekstra, Pieter J., Morgan, Thomas M., Loring, Erin, Yasuno, Katsuhito, Fernandez, Thomas, Sanders, Stephan, Louvi, Angeliki, Cho, Judy H., Mane, Shrikant, Colangelo, Christopher M., Biederer, Thomas, Lifton, Richard P., Gunel, Murat, State, Matthew W.
منشور في 2010

De novo mutations revealed by whole exome sequencing are strongly associated with autism

بواسطة Sanders, Stephan J., Murtha, Michael T., Gupta, Abha R., Murdoch, John D., Raubeson, Melanie J., Willsey, A. Jeremy, Ercan-Sencicek, A. Gulhan, DiLullo, Nicholas M., Parikshak, Neelroop N., Stein, Jason L., 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., Meyer, Kyle A., Bilguvar, Kaya, Mane, Shrikant M., Šestan, Nenad, Lifton, Richard P., Günel, Murat, Roeder, Kathryn, Geschwind, Daniel H., Devlin, Bernie, State, Matthew W.
منشور في 2012

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

بواسطة 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, Han, Wenqi, He, Xin, Hoffman, Ellen, Klei, Lambertus, Lei, Jing, Liu, Wenzhong, Liu, Li, Lu, Cong, Xu, Xuming, Zhu, Ying, Mane, Shrikant M., Lein, Edward S., Wei, Liping, Noonan, James P., Roeder, Kathryn, Devlin, Bernie, Šestan, Nenad, State, Matthew W.
منشور في 2013

Integrated genomic characterization of IDH1-mutant glioma malignant progression

بواسطة Bai, Hanwen, Harmanci, Akdes Serin, Erson-Omay, E Zeynep, Li, Jie, Coşkun, Süleyman, Simon, Matthias, Krischek, Boris, Özduman, Koray, Omay, S Bülent, Sorensen, Eric A, Turcan, Şevin, Bakırcığlu, Mehmet, Carrión-Grant, Geneive, Murray, Phillip B, Clark, Victoria E, Ercan-Sencicek, A Gulhan, Knight, James, Sencar, Leman, Altınok, Selin, Kaulen, Leon D, Gülez, Burcu, Timmer, Marco, Schramm, Johannes, Mishra-Gorur, Ketu, Henegariu, Octavian, Moliterno, Jennifer, Louvi, Angeliki, Chan, Timothy A, Tannheimer, Stacey L, Pamir, M Necmettin, Vortmeyer, Alexander O, Bilguvar, Kaya, Yasuno, Katsuhito, Günel, Murat
الحاوية / القاعدة Nat Genet (2015)

De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder

بواسطة 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, John F., Teran, Nicole A., Dea, Jeanselle, Mandell, Jeffrey D., Bal, Vanessa Hus, 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.
منشور في 2014

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

بواسطة 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.
الحاوية / القاعدة Neuron (2015)