Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
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Glutathione S-transferase M1 or T1 null genotype as a risk factor for developing multiple primary neoplasms in the upper aero-digestive tract, in Indian males using tobacco. Oral oncology 2004 Jan 40 (1): 84-91. Jhavar Sameer, Sarin Rajiv, Mulherkar Rita, Benner Axel, Agarwal Jai Prakash, Dinshaw Ketay |
Variants of the SLC6A3 (DAT1) polymorphism affect performance monitoring-related cortical evoked potentials that are associated with ADHD. Biological psychology 2010 Sep 85 (1): 19-32. Althaus Monika, Groen Yvonne, Wijers Albertus A, Minderaa Ruud B, Kema Ido P, Dijck Janneke D A, Hoekstra Pieter |
[Association between Tbx20 gene polymorphism and congenital atrial septal defects]. Zhonghua nei ke za zhi 2015 Oct 54 (10): 860-4. Ma Yulong, Xiang Yang, Li Xiaomei, Yang Yining, Ma Yitong, Xie Xiang, Liu F |
Genome-wide association meta-analyses identified 1q43 and 2q32.2 for hip Ward's triangle areal bone mineral density.
Bone 2016 Oct 91 1-10. Pei Yu-Fang, Hu Wen-Zhu, Hai Rong, Wang Xiu-Yan, Ran Shu, Lin Yong, Shen Hui, Tian Qing, , , , Lei Shu-Feng, Zhang Yong-Hong, Papasian Christopher J, Deng Hong-Wen, Zhang L |
Clinical significance of type 2 iodothyronine deiodinase polymorphism. Expert review of endocrinology & metabolism 2018 9 13 (5): 273-277. Maino Fabio, Cantara Silvia, Forleo Raffaella, Pilli Tania, Castagna Maria Graz |
Toll-Interleukin 1 Receptor Domain-Containing Adaptor Protein 180L Single-Nucleotide Polymorphism Is Associated With Susceptibility to Recurrent Pneumococcal Lower Respiratory Tract Infections in Children. Frontiers in immunology 2018 9 1780. Siebert Johan N, Hamann Lutz, Verolet Charlotte M, Gameiro Cécile, Grillet Stéphane, Siegrist Claire-Anne, Posfay-Barbe Klara |
Molecular alterations associated with metastases of solid pseudopapillary neoplasms of the pancreas. The Journal of pathology 2018 10 247 (1): 123-134. Amato Eliana, Mafficini Andrea, Hirabayashi Kenichi, Lawlor Rita T, Fassan Matteo, Vicentini Caterina, Barbi Stefano, Delfino Pietro, Sikora Katarzyna, Rusev Borislav, Simbolo Michele, Esposito Irene, Antonello Davide, Pea Antonio, Sereni Elisabetta, Ballotta Maria, Maggino Laura, Marchegiani Giovanni, Ohike Nobuyuki, Wood Laura D, Salvia Roberto, Klöppel Günter, Zamboni Giuseppe, Scarpa Aldo, Corbo Vincen |
Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes. Genome medicine 2021 Oct 13 (1): 172. Vysotskiy Mikhail, Zhong Xue, Miller-Fleming Tyne W, Zhou Dan, , , , Cox Nancy J, Weiss Lauren |
Bilateral atrophy of the extensor digitorum brevis muscle might be a useful sign for diagnosing diabetic polyneuropathy in Japanese men who do not sit in the traditional "seiza" style. Journal of diabetes investigation 2021 1 12 (3): 398-408. Kishimoto Shohei, Sasaki Hideyuki, Kurisu Seigo, Ogawa Kenichi, Matsuno Shohei, Furuta Hiroto, Arita Mikio, Naka Keigo, Nanjo Kishio, Akamizu Takas |
Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts. NPJ genomic medicine 2022 Jun 7 (1): 38. Giannuzzi Giuliana, Chatron Nicolas, Mannik Katrin, Auwerx Chiara, Pradervand Sylvain, Willemin Gilles, Hoekzema Kendra, Nuttle Xander, Chrast Jacqueline, Sadler Marie C, Porcu Eleonora, , Herault Yann, Isidor Bertrand, Gilbert-Dussardier Brigitte, Eichler Evan E, Kutalik Zoltan, Reymond Alexand |
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