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

af Negron, Steven G., Ercan-Sencicek, A. Gulhan, Freed, Jessica, Walters, Madeline, Lin, Zhiqiang
Udgivet i Sci Rep (2020)

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

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

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

af 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.
Udgivet 2011

Engineering spatial-organized cardiac organoids for developmental toxicity testing

af 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
Udgivet i Stem Cell Reports (2021)

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

af 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.
Udgivet 2011

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

af 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.
Udgivet 2011

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

af 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
Udgivet i Eur J Hum Genet (2015)

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

af 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.
Udgivet 2008

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

af 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.
Udgivet i Am J Hum Genet (2016)

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

af 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.
Udgivet 2012

Neurogenetic analysis of childhood disintegrative disorder

af 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.
Udgivet i Mol Autism (2017)

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

af 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
Udgivet 2014

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

af 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
Udgivet 2011

Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas

af 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
Udgivet i Nat Genet (2016)

l-Histidine Decarboxylase and Tourette's Syndrome

af 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.
Udgivet 2010

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

af 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.
Udgivet 2012

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

af 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.
Udgivet 2013

Integrated genomic characterization of IDH1-mutant glioma malignant progression

af 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
Udgivet i Nat Genet (2015)

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

af 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.
Udgivet 2014

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

af 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.
Udgivet i Neuron (2015)