Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: SATB2[original query] |
---|
Medical sequencing of candidate genes for nonsyndromic cleft lip and palate. PLoS genetics 2005 Dec 1 (6): e64. Vieira Alexandre R, Avila Joseph R, Daack-Hirsch Sandra, Dragan Ecaterina, Félix Têmis M, Rahimov Fedik, Harrington Jill, Schultz Rebecca R, Watanabe Yoriko, Johnson Marla, Fang Jennifer, O'Brien Sarah E, Orioli Iêda M, Castilla Eduardo E, Fitzpatrick David R, Jiang Rulang, Marazita Mary L, Murray Jeffrey |
Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations. Human genetics 2006 Nov 120 (4): 501-18. Beaty T H, Hetmanski J B, Fallin M D, Park J W, Sull J W, McIntosh I, Liang K Y, Vanderkolk C A, Redett R J, Boyadjiev S A, Jabs E W, Chong S S, Cheah F S H, Wu-Chou Y H, Chen P K, Chiu Y F, Yeow V, Ng I S L, Cheng J, Huang S, Ye X, Wang H, Ingersoll R, Scott A |
Testing reported associations of genetic risk factors for oral clefts in a large Irish study population. Birth defects research. Part A, Clinical and molecular teratology 2010 Feb 88 (2): 84-93. Carter Tonia C, Molloy Anne M, Pangilinan Faith, Troendle James F, Kirke Peadar N, Conley Mary R, Orr David J A, Earley Michael, McKiernan Eamon, Lynn Ena C, Doyle Anne, Scott John M, Brody Lawrence C, Mills James |
The clinical significance of small copy number variants in neurodevelopmental disorders. Journal of medical genetics 2014 Oct 51 (10): 677-88. Asadollahi Reza, Oneda Beatrice, Joset Pascal, Azzarello-Burri Silvia, Bartholdi Deborah, Steindl Katharina, Vincent Marie, Cobilanschi Joana, Sticht Heinrich, Baldinger Rosa, Reissmann Regina, Sudholt Irene, Thiel Christian T, Ekici Arif B, Reis André, Bijlsma Emilia K, Andrieux Joris, Dieux Anne, FitzPatrick David, Ritter Susanne, Baumer Alessandra, Latal Beatrice, Plecko Barbara, Jenni Oskar G, Rauch Ani |
Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation. Journal of human genetics 2015 Jan 60 (1): 17-25. Simioni Milena, Araujo Tânia Kawasaki, Monlleo Isabella Lopes, Maurer-Morelli Cláudia Vianna, Gil-da-Silva-Lopes Vera Lúc |
SATB2 gene variants in non-syndromic cleft lip with or without cleft palate in Indian population. Journal of oral biology and craniofacial research 0 5 (3): 161-164. Gurramkonda Venkatesh Babu, Syed Altaf Hussain, Murthy Jyotsna, Lakkakula Bhaskar V K |
Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts. Human genetics 2015 Nov . Conte Federica, Oti Martin, Dixon Jill, Carels Carine E L, Rubini Michele, Zhou Huiqi |
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis.
The Lancet. Oncology 2016 Aug . Gharahkhani Puya, Fitzgerald Rebecca C, Vaughan Thomas L, Palles Claire, Gockel Ines, Tomlinson Ian, Buas Matthew F, May Andrea, Gerges Christian, Anders Mario, Becker Jessica, Kreuser Nicole, Noder Tania, Venerito Marino, Veits Lothar, Schmidt Thomas, Manner Hendrik, Schmidt Claudia, Hess Timo, Böhmer Anne C, Izbicki Jakob R, Hölscher Arnulf H, Lang Hauke, Lorenz Dietmar, Schumacher Brigitte, Hackelsberger Andreas, Mayershofer Rupert, Pech Oliver, Vashist Yogesh, Ott Katja, Vieth Michael, Weismüller Josef, Nöthen Markus M, , , , Attwood Stephen, Barr Hugh, Chegwidden Laura, de Caestecker John, Harrison Rebecca, Love Sharon B, MacDonald David, Moayyedi Paul, Prenen Hans, Watson R G Peter, Iyer Prasad G, Anderson Lesley A, Bernstein Leslie, Chow Wong-Ho, Hardie Laura J, Lagergren Jesper, Liu Geoffrey, Risch Harvey A, Wu Anna H, Ye Weimin, Bird Nigel C, Shaheen Nicholas J, Gammon Marilie D, Corley Douglas A, Caldas Carlos, Moebus Susanne, Knapp Michael, Peters Wilbert H M, Neuhaus Horst, Rösch Thomas, Ell Christian, MacGregor Stuart, Pharoah Paul, Whiteman David C, Jankowski Janusz, Schumacher Johann |
Genetic Interactions in Nonsyndromic Orofacial Clefts in Europe-EUROCRAN Study. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2016 Dec . Mossey Peter A, Little Julian, Steegers-Theunissen Regine, Molloy Anne, Peterlin Borut, Shaw William C, Johnson Candice, FitzPatrick David R, Franceschelli Paola, Rubini Miche |
Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2016 Oct . Whitton Laura, Cosgrove Donna, Clarkson Christopher, Harold Denise, Kendall Kimberley, Richards Alex, Mantripragada Kiran, Owen Michael J, O'Donovan Michael C, Walters James, Hartmann Annette, Konte Betina, Rujescu Dan, , Gill Michael, Corvin Aiden, Rea Stephen, Donohoe Gary, Morris Derek |
Candidate gene analyses of 3-dimensional dentoalveolar phenotypes in subjects with malocclusion. American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics 2017 Mar 151 (3): 539-558. Weaver Cole A, Miller Steven F, da Fontoura Clarissa S G, Wehby George L, Amendt Brad A, Holton Nathan E, Allareddy Veeratrishul, Southard Thomas E, Moreno Uribe Lina |
Genes regulated by SATB2 during neurodevelopment contribute to schizophrenia and educational attainment. PLoS genetics 2018 7 14 (7): e1007515. Whitton Laura, Apostolova Galina, Rieder Dietmar, Dechant Georg, Rea Stephen, Donohoe Gary, Morris Derek |
High-throughput identification of noncoding functional SNPs via type IIS enzyme restriction. Nature genetics 2018 7 50 (8): 1180-1188. Li Gang, Martínez-Bonet Marta, Wu Di, Yang Yu, Cui Jing, Nguyen Hung N, Cunin Pierre, Levescot Anaïs, Bai Ming, Westra Harm-Jan, Okada Yukinori, Brenner Michael B, Raychaudhuri Soumya, Hendrickson Eric A, Maas Richard L, Nigrovic Peter |
Association between SATB2 gene polymorphism and cleft palate only risk in eastern Guangdong population and a meta-analysis. Cellular and molecular biology (Noisy-le-Grand, France) 2018 Nov 64 (14): 101-107. Zhang Wancong, Tan Linwang, Xing Yue, Zhao Hanxing, Shi Lungang, Zhou Jianda, Lang Xing, Cai Jianxiong, Tang Shij |
Exploring different impaired speed of genetic-related brain function and structures in schizophrenic progress using multimodal analysis. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference 2018 11 2018 4126-4129. Luo Na, Tian Lin, Calhoun Vince D, Chen Jiayu, Lin Dongdong, Vergara Victor M, Rao Shuquan, Zhang Fuquan, Sui Ji |
Common variants in SATB2 are associated with schizophrenia in Uygur Chinese population. Psychiatric genetics 2019 May . Zhou Juan, Chen Jianhua, Xu Wei, Liu Yahui, Song Zhijian, Wen Zujia, Jian Xuemin, Yu Jiezhong, Ma Xiaojun, Wang Zhuo, Pan Dun, Yi Qizhong, Shi Yongyo |
Two types of primary mucinous ovarian tumors can be distinguished based on their origin. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2019 Nov . Simons Michiel, Simmer Femke, Bulten Johan, Ligtenberg Marjolijn J, Hollema Harry, van Vliet Shannon, de Voer Richarda M, Kamping Eveline J, van Essen Dirk F, Ylstra Bauke, Schwartz Lauren E, Wang Yihong, Massuger Leon F, Nagtegaal Iris D, Kurman Robert |
Metastatic colorectal carcinomas with high SATB2 expression are associated with better prognosis and response to chemotherapy: a population-based Scandinavian study. Acta oncologica (Stockholm, Sweden) 2019 11 59 (3): 284-290. Mezheyeuski Artur, Ponten Fredrik, Edqvist Per-Henrik, Sundström Magnus, Thunberg Ulf, Qvortrup Camilla, Pfeiffer Per, Sorbye Halfdan, Glimelius Bengt, Dragomir An |
Looking for Sunshine: Genetic Predisposition to Sun Seeking in 265,000 Individuals of European Ancestry.
The Journal of investigative dermatology 2020 (4): 779-786. Sanna Marianna, Li Xin, Visconti Alessia, Freidin Maxim B, Sacco Chiara, Ribero Simone, Hysi Pirro, Bataille Veronique, Han Jiali, Falchi Mar |
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2. Clinical genetics 2020 12 99 (4): 547-557. Zarate Yuri A, Bosanko Katherine A, Thomas Mary Ann, Miller David T, Cusmano-Ozog Kristina, Martinez-Monseny Antonio, Curry Cynthia J, Graham John M, Velsher Lea, Bekheirnia Mir Reza, Seidel Veronica, Dedousis Demitrios, Mitchell Anna L, DiMarino Amy M, Riess Angelika, Balasubramanian Meena, Fish Jennifer L, Caffrey Aisling R, Fleischer Nicole, Pierson Tyler Mark, Lacro Ronald |
Whole genome sequencing of 45 Japanese patients with intellectual disability. American journal of medical genetics. Part A 2021 2 185 (5): 1468-1480. Abe-Hatano Chihiro, Iida Aritoshi, Kosugi Shunichi, Momozawa Yukihide, Terao Chikashi, Ishikawa Keiko, Okubo Mariko, Hachiya Yasuo, Nishida Hiroya, Nakamura Kazuyuki, Miyata Rie, Murakami Chie, Takahashi Kan, Hoshino Kyoko, Sakamoto Haruko, Ohta Sayaka, Kubota Masaya, Takeshita Eri, Ishiyama Akihiko, Nakagawa Eiji, Sasaki Masayuki, Kato Mitsuhiro, Matsumoto Naomichi, Kamatani Yoichiro, Kubo Michiaki, Takahashi Yoshiyuki, Natsume Jun, Inoue Ken, Goto Yu-Ic |
New genes involved in Angelman syndrome-like: Expanding the genetic spectrum. PloS one 2021 16 (10): e0258766. Aguilera Cinthia, Gabau Elisabeth, Ramirez-Mallafré Ariadna, Brun-Gasca Carme, Dominguez-Carral Jana, Delgadillo Veronica, Laurie Steve, Derdak Sophia, Padilla Natàlia, de la Cruz Xavier, Capdevila Núria, Spataro Nino, Baena Neus, Guitart Miriam, Ruiz An |
Associations of cognitive impairment in patients with schizophrenia with genetic features and with schizophrenia-related structural and functional brain changes. Frontiers in genetics 2022 13 880027. Zhuo Chuanjun, Tian Hongjun, Chen Jiayue, Li Qianchen, Yang Lei, Zhang Qiuyu, Chen Guangdong, Cheng Langlang, Zhou Chunhua, Song Xueq |
A shared genetic architecture between adhesive capsulitis and Dupuytren disease. Journal of shoulder and elbow surgery 2022 Aug . Kim Stuart K, Khan Condor, Ladd Amy L, Tashjian Robert |
Identification of novel susceptibility genes for non-syndromic cleft lip with or without cleft palate using NGS-based multigene panel testing. Molecular genetics and genomics : MGG 2022 Jul . D?browska Justyna, Biedziak Barbara, Szponar-?urowska Anna, Budner Margareta, Jagodzi?ski Pawe? P, P?oski Rafa?, Mostowska Adrian |
Mendelian etiologies identified with whole exome sequencing in cerebral palsy. Annals of clinical and translational neurology 2022 1 9 (2): 193-205. Chopra Maya, Gable Dustin L, Love-Nichols Jamie, Tsao Alexa, Rockowitz Shira, Sliz Piotr, Barkoudah Elizabeth, Bastianelli Lucia, Coulter David, Davidson Emily, DeGusmao Claudio, Fogelman David, Huth Kathleen, Marshall Paige, Nimec Donna, Sanders Jessica Solomon, Shore Benjamin J, Snyder Brian, Stone Scellig S D, Ubeda Ana, Watkins Colyn, Berde Charles, Bolton Jeffrey, Brownstein Catherine, Costigan Michael, Ebrahimi-Fakhari Darius, Lai Abbe, O'Donnell-Luria Anne, Paciorkowski Alex R, Pinto Anna, Pugh John, Rodan Lance, Roe Eugene, Swanson Lindsay, Zhang Bo, Kruer Michael C, Sahin Mustafa, Poduri Annapurna, Srivastava Siddhar |
Comprehensive clinicopathologic, molecular, and immunologic characterization of colorectal carcinomas with loss of three intestinal markers, CDX2, SATB2, and KRT20. Virchows Archiv : an international journal of pathology 2022 1 480 (3): 543-555. Lee Ji Ae, Seo Mi-Kyoung, Yoo Seung-Yeon, Cho Nam-Yun, Kwak Yoonjin, Lee Kyoungbun, Kim Jung Ho, Kang Gyeong Ho |
SATB2 organizes the 3D genome architecture of cognition in cortical neurons. Molecular cell 2024 1 . Nico Wahl, Sergio Espeso-Gil, Paola Chietera, Amelie Nagel, Aodán Laighneach, Derek W Morris, Prashanth Rajarajan, Schahram Akbarian, Georg Dechant, Galina Apostolo |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: