Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: MLC1[original query] |
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MLC1 gene is associated with schizophrenia and bipolar disorder in Southern India. Biological psychiatry 2005 Jul 58 (1): 16-22. Verma Ranjana, Mukerji Mitali, Grover Deepak, B-Rao Chandrika, Das Swapan Kumar, Kubendran Shobana, Jain Sanjeev, Brahmachari Samir |
MLC1 polymorphisms are specifically associated with periodic catatonia, a subgroup of chronic schizophrenia. Biological psychiatry 2007 May 61 (10): 1211-4. Selch Sandra, Strobel Alexander, Haderlein Julia, Meyer Jobst, Jacob Christian P, Schmitt Angelika, Lesch Klaus-Peter, Reif Andre |
Influence of differentially expressed genes from suicide post-mortem study on personality traits as endophenotypes on healthy subjects and suicide attempters. European archives of psychiatry and clinical neuroscience 2014 Aug 264 (5): 423-32. Calati Raffaella, Giegling Ina, Balestri Martina, Antypa Niki, Friedl Marion, Konte Bettina, Hartmann Annette M, Serretti Alessandro, Rujescu D |
Molecular Diagnosis of Hereditary Fructose Intolerance: Founder Mutation in a Community from India. JIMD reports 2015 1 19 85-93. Bijarnia-Mahay Sunita, Movva Sireesha, Gupta Neerja, Sharma Deepak, Puri Ratna D, Kotecha Udhaya, Saxena Renu, Kabra Madhulika, Mohan Neelam, Verma Ishwar |
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.
PLoS genetics 2017 Apr 13 (4): e1006719. Ng Maggie C Y, Graff Mariaelisa, Lu Yingchang, Justice Anne E, Mudgal Poorva, Liu Ching-Ti, Young Kristin, Yanek Lisa R, Feitosa Mary F, Wojczynski Mary K, Rand Kristin, Brody Jennifer A, Cade Brian E, Dimitrov Latchezar, Duan Qing, Guo Xiuqing, Lange Leslie A, Nalls Michael A, Okut Hayrettin, Tajuddin Salman M, Tayo Bamidele O, Vedantam Sailaja, Bradfield Jonathan P, Chen Guanjie, Chen Wei-Min, Chesi Alessandra, Irvin Marguerite R, Padhukasahasram Badri, Smith Jennifer A, Zheng Wei, Allison Matthew A, Ambrosone Christine B, Bandera Elisa V, Bartz Traci M, Berndt Sonja I, Bernstein Leslie, Blot William J, Bottinger Erwin P, Carpten John, Chanock Stephen J, Chen Yii-Der Ida, Conti David V, Cooper Richard S, Fornage Myriam, Freedman Barry I, Garcia Melissa, Goodman Phyllis J, Hsu Yu-Han H, Hu Jennifer, Huff Chad D, Ingles Sue A, John Esther M, Kittles Rick, Klein Eric, Li Jin, McKnight Barbara, Nayak Uma, Nemesure Barbara, Ogunniyi Adesola, Olshan Andrew, Press Michael F, Rohde Rebecca, Rybicki Benjamin A, Salako Babatunde, Sanderson Maureen, Shao Yaming, Siscovick David S, Stanford Janet L, Stevens Victoria L, Stram Alex, Strom Sara S, Vaidya Dhananjay, Witte John S, Yao Jie, Zhu Xiaofeng, Ziegler Regina G, Zonderman Alan B, Adeyemo Adebowale, Ambs Stefan, Cushman Mary, Faul Jessica D, Hakonarson Hakon, Levin Albert M, Nathanson Katherine L, Ware Erin B, Weir David R, Zhao Wei, Zhi Degui, , Arnett Donna K, Grant Struan F A, Kardia Sharon L R, Oloapde Olufunmilayo I, Rao D C, Rotimi Charles N, Sale Michele M, Williams L Keoki, Zemel Babette S, Becker Diane M, Borecki Ingrid B, Evans Michele K, Harris Tamara B, Hirschhorn Joel N, Li Yun, Patel Sanjay R, Psaty Bruce M, Rotter Jerome I, Wilson James G, Bowden Donald W, Cupples L Adrienne, Haiman Christopher A, Loos Ruth J F, North Kari |
Nine differentially expressed genes from a post mortem study and their association with suicidal status in a sample of suicide completers, attempters and controls. Journal of psychiatric research 2017 Mar 91 98-104. Balestri Martina, Crisafulli Concetta, Donato Luigi, Giegling Ina, Calati Raffaella, Antypa Niki, Schneider Barbara, Marusic Dragan, Tarozzi Maria Eugenia, Marusic Dorjan, Paragi Metka, Hartmann Annette M, Konte Bettina, Marsano Agnese, Serretti Alessandro, Rujescu D |
Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis. Annals of neurology 2018 Jun . Jia Xiaoming, Madireddy Lohith, Caillier Stacy, Santaniello Adam, Esposito Federica, Comi Giancarlo, Stuve Olaf, Zhou Yuan, Taylor Bruce, Kilpatrick Trevor, Martinelli-Boneschi Filippo, Cree Bruce A C, Oksenberg Jorge R, Hauser Stephen L, Baranzini Sergio |
Novel variants causing megalencephalic leukodystrophy in Sudanese families. Journal of human genetics 2021 Sep . Amin Mutaz, Vignal Cedric, Hamed Ahlam A A, Mohammed Inaam N, Elseed Maha A, Drunat Severine, Babai Arwa, Eltaraifee Esraa, Elbadi Iman, Abubaker Rayan, Mustafa Doaa, Yahia Ashraf, Koko Mahmoud, Osman Melka, Bakhit Yousuf, Elshafea Azza, Alsiddig Mohamed, Haroun Sahwah, Lelay Gurvan, Elsayed Liena E O, Ahmed Ammar E, Boespflug-Tanguy Odile, Dorboz Im |
Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families. Brain & development 2022 4 44 (7): 454-461. Khalaf-Nazzal Reham, Dweikat Imad, Maree Mosab, Alawneh Maysa, Barahmeh Myassar, Doulani Rasha T, Qrareya Mohammad, Qadi Mohammad, Dudin Anw |
Machine Learning Study of SNPs in Noncoding Regions to Predict Non-small Cell Lung Cancer Susceptibility. Clinical oncology (Royal College of Radiologists (Great Britain)) 2023 9 . Y Huang, T Bao, T Zhang, G Ji, Y Wang, Z Ling, W |
MLC1 Overexpression Inhibits Tumor Progression through PI3K/AKT Signal Pathway in Prostate Cancer. Advanced biology 2023 10 e2300060. Zonglin Wu, Jinliang Ni, Houliang Zhang, Yifan Zhang, Chengxun Lv, Yidi Wang, Keyi Wang, Bo Pe |
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- Page last updated:May 06, 2024
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