Human Genome Epidemiology Literature Finder
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Records 1 - 26 (of 26 Records) |
| Query Trace: NOG[original query] |
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Genetics implicates overactive osteogenesis in the development of diffuse idiopathic skeletal hyperostosis.
Nature communications 2023 5 14 (1): 2644. Sethi Anurag, Ruby J Graham, Veras Matthew A, Telis Natalie, Melamud Euge |
| Evaluation of BMP4 and its specific inhibitor NOG as candidates in human neural tube defects (NTDs). European journal of human genetics : EJHG 2002 Nov 10 (11): 753-6. Felder Bärbel, Stegmann Karolin, Schultealbert Almut, Geller Frank, Strehl Elisabeth, Ermert August, Koch Manuela |
| Identification and association analysis of single nucleotide polymorphisms in the human noggin (NOG) gene and osteoporosis phenotypes. Bone 2009 May 44 (5): 999-1002. Moffett Susan P, Dillon Katie A, Yerges Laura M, Goodrich Louis J, Nestlerode Cara, Bunker Clareann H, Wheeler Victor W, Patrick Alan L, Zmuda Joseph |
| Mutational analysis of NOG in esophageal atresia and tracheoesophageal fistula patients. Pediatric surgery international 2012 Apr 28 (4): 335-40. Murphy Andrew J, Li Yina, Pietsch Joshua B, Chiang Chin, Lovvorn Harold |
| Peripheral blood gene expression as a novel genomic biomarker in complicated sarcoidosis. PloS one 2012 7 (9): e44818. Zhou Tong, Zhang Wei, Sweiss Nadera J, Chen Edward S, Moller David R, Knox Kenneth S, Ma Shwu-Fan, Wade Michael S, Noth Imre, Machado Roberto F, Garcia Joe G |
| Chiari malformation type I: a case-control association study of 58 developmental genes. PloS one 2013 8 (2): e57241. Urbizu Aintzane, Toma Claudio, Poca Maria A, Sahuquillo Juan, Cuenca-León Ester, Cormand Bru, Macaya Alfo |
| Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians. American journal of medical genetics. Part A 2014 Oct 164A (10): 2572-80. Figueiredo Jane C, Ly Stephanie, Raimondi Haley, Magee Kathy, Baurley James W, Sanchez-Lara Pedro A, Ihenacho Ugonna, Yao Caroline, Edlund Christopher K, van den Berg David, Casey Graham, DeClerk Yves A, Samet Jonathan M, Magee Willi |
| Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathway. Birth defects research. Part A, Clinical and molecular teratology 2014 Jun 100 (6): 493-8. Al Chawa Taofik, Ludwig Kerstin U, Fier Heide, Pötzsch Bernd, Reich Rudolf H, Schmidt Gül, Braumann Bert, Daratsianos Nikolaos, Böhmer Anne C, Schuencke Hannah, Alblas Margrieta, Fricker Nadine, Hoffmann Per, Knapp Michael, Lange Christoph, Nöthen Markus M, Mangold Elisabe |
| Association between NOGGIN and SPRY2 polymorphisms and nonsyndromic cleft lip with or without cleft palate. American journal of medical genetics. Part A 2015 Jan 167A (1): 137-41. Song Tao, Shi Jinna, Guo Qiang, Lv Kewen, Jiao Xiaohui, Hu Tenglong, Sun Xiangyu, Fu Songb |
| Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci. American journal of human genetics 2015 Mar 96 (3): 397-411. Leslie Elizabeth J, Taub Margaret A, Liu Huan, Steinberg Karyn Meltz, Koboldt Daniel C, Zhang Qunyuan, Carlson Jenna C, Hetmanski Jacqueline B, Wang Hang, Larson David E, Fulton Robert S, Kousa Youssef A, Fakhouri Walid D, Naji Ali, Ruczinski Ingo, Begum Ferdouse, Parker Margaret M, Busch Tamara, Standley Jennifer, Rigdon Jennifer, Hecht Jacqueline T, Scott Alan F, Wehby George L, Christensen Kaare, Czeizel Andrew E, Deleyiannis Frederic W-B, Schutte Brian C, Wilson Richard K, Cornell Robert A, Lidral Andrew C, Weinstock George M, Beaty Terri H, Marazita Mary L, Murray Jeffrey |
| Rare copy number variants identified in prune belly syndrome. European journal of medical genetics 2017 11 61 (3): 145-151. Boghossian Nansi S, Sicko Robert J, Giannakou Andreas, Dimopoulos Aggeliki, Caggana Michele, Tsai Michael Y, Yeung Edwina H, Pankratz Nathan, Cole Benjamin R, Romitti Paul A, Browne Marilyn L, Fan Ruzong, Liu Aiyi, Kay Denise M, Mills James |
| NTN1 gene was risk to non-syndromic cleft lip only among Han Chinese population. Oral diseases 2019 Mar 25 (2): 535-542. Jiang ShuYuan, Shi Jia-Yu, Lin Yan-Song, Duan Shi-Jun, Chen Xieli, Jiao Jian-Jun, Shen Wei, Jin Xiaoju, You Miao, Wang Moyao, Shi Bing, Jia Zhong-L |
| Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation. Frontiers in genetics 2018 11 9 502. Indencleef Karlijne, Roosenboom Jasmien, Hoskens Hanne, White Julie D, Shriver Mark D, Richmond Stephen, Peeters Hilde, Feingold Eleanor, Marazita Mary L, Shaffer John R, Weinberg Seth M, Hens Greet, Claes Pet |
| SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis. Genetics in medicine : official journal of the American College of Medical Genetics 2019 May . Yang Yongjia, Zheng Yu, Li Wangming, Li Liping, Tu Ming, Zhao Liu, Mei Haibo, Zhu Guanghui, Zhu Yim |
| The SLAMF3 rs509749 polymorphism correlates with malignant potential in multiple myeloma. Experimental hematology 2020 Aug . Ishibashi Mariko, Sunakawa-Kii Mika, Kaito Yuta, Kinoshita Ryosuke, Asayama Toshio, Kuribayashi Yasuko, Inokuchi Koiti, Morita Rimpei, Tamura Hide |
| Genetic determinants of fracture non-union: A systematic review from the literature. Gene 2020 5 751 144766. Yan Ting, Li Jin, Zhou Xindie, Yang Zhicheng, Zhang Yi, Zhang Junjie, Xu Nanwei, Huang Yong, Yang Hao |
| Association Between Nonsyndromic Cleft Lip and Palate and 2 Polymorphic Loci: A Meta-Analysis. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2020 10 58 (6): 763-772. Wang Yusi, Jia Xueyuan, Qiao Yuandong, Xu Lidan, Zhang Xuelong, Li Qiuyan, Wang Ping, Sun Wenjing, Wu J |
| Preliminary study of genome-wide association identified novel susceptibility genes for thyroid-related hormones in Chinese population. Genes & genomics 2021 Sep . Huang Liang, Bai Fenghua, Zhang Yutian, Zhang Shanshan, Jin Tianbo, Wei Xingwei, Zhou Xiaoli, Lin Mei, Xie Yufei, He Chanyi, Lin Qi, Xie Tian, Ding Yipe |
| Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity.
International journal of obesity (2005) 2021 . Liu Yaowu, Zhang Xiaoyu, Lee Jiwon, Smelser Diane, Cade Brian, Chen Han, Zhou Hufeng, Kirchner H Lester, Lin Xihong, Mukherjee Sutapa, Hillman David, Liu Ching-Ti, Redline Susan, Sofer Tam |
| Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.
PLoS genetics 2021 7 17 (7): e1009584. Ray Debashree, Venkataraghavan Sowmya, Zhang Wanying, Leslie Elizabeth J, Hetmanski Jacqueline B, Weinberg Seth M, Murray Jeffrey C, Marazita Mary L, Ruczinski Ingo, Taub Margaret A, Beaty Terri |
| Association of genetic polymorphisms of VAX1, MAFB, and NTN1 with nonsyndromic cleft lip with or without cleft palate in Chinese population. Molecular genetics and genomics : MGG 2022 Feb . Peng Li, Niu Zhenmin, Chen Jiapei, Wan Teng, Wu Dandan, Yang Yusheng, Wang Guomin, Yang Lin, Huang Wei, Chen Zhen |
| In silico identification of the specific pathways in each stage of colorectal cancer and the association of their top genes with drug resistance and sensitivity. Medical oncology (Northwood, London, England) 2022 2 39 (5): 57. Hashemi Reza, Peymani Maryam, Ghaedi Kamran, Saffar Ha |
| Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis. Scientific reports 2022 1 12 (1): 1214. Slavec Lara, Karas Kuželi?ki Nataša, Locatelli Igor, Geršak Kseni |
| Ethnic Differences in the Brazilian Population Influence the Impact of BMP4 Genetic Variants on Susceptibility of Nonsyndromic Orofacial Clefts. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2023 6 10556656231180086. Lilianny Querino Rocha de Oliveira, Hellen Carolliny de Souza Nicolau, Daniella Reis Barbosa Martelli, Hercílio Martelli-Júnior, Rafaela Scariot, Ana Lúcia Carrinho Ayroza Rangel, Silvia Regina de Almeida Reis, Ricardo D Coletta, Renato Assis Macha |
| Genetic Influence of Fracture Nonunion (FNU): A Systematic Review. Pharmacogenomics and personalized medicine 2023 6 16 569-575. Mir Sadat-Ali, Hussain K Al-Omar, Khalid W AlTabash, Ammar K AlOmran, Dakheel A AlDakheel, Hasan N AlSay |
| Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia. Croatian medical journal 2024 6 65 (3): 198-208. Ivona Sansovi?, Ana-Maria Meaši?, Adriana Bobinec, Leona Morožin Pohovski, Ljubica Odak, Katarina Vulin, Bernarda Lozi?, Mijana Kero, Sanda Huljev Frkovi?, Silvija Pušelj |
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