Literature DB >> 27898081

Understanding unspecific complaints through genetics.

Eli Sprecher1.   

Abstract

Unspecific and unexplained medical complaints can be frustrating to both patients and clinicians. A cause for these complex symptoms and signs may now have been identified.

Entities:  

Year:  2016        PMID： 27898081     DOI： 10.1038/ng.3730

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


  9 in total

Review 1.  Spectrum of mast cell activation disorders.

Authors:  Anastasia I Petra; Smaro Panagiotidou; Julia M Stewart; Pio Conti; Theoharis C Theoharides
Journal:  Expert Rev Clin Immunol       Date:  2014-05-01       Impact factor: 4.473

Review 2.  A systematic review and meta-analysis of the percentage of revised diagnoses in functional somatic symptoms.

Authors:  E M Eikelboom; L M Tak; A M Roest; J G M Rosmalen
Journal:  J Psychosom Res       Date:  2016-07-25       Impact factor: 3.006

Review 3.  Human mast cell tryptase in biology and medicine.

Authors:  Joana Vitte
Journal:  Mol Immunol       Date:  2014-05-03       Impact factor: 4.407

4.  Serotonin transporter gene (SLC6A4) polymorphism in patients with irritable bowel syndrome and healthy controls.

Authors:  Sunil Kumar; Prabhat Ranjan; Balraj Mittal; Uday C Ghoshal
Journal:  J Gastrointestin Liver Dis       Date:  2012-03       Impact factor: 2.008

5.  First evidence for an association of a functional variant in the microRNA-510 target site of the serotonin receptor-type 3E gene with diarrhea predominant irritable bowel syndrome.

Authors:  Johannes Kapeller; Lesley A Houghton; Hubert Mönnikes; Jutta Walstab; Dorothee Möller; Heinz Bönisch; Barbara Burwinkel; Frank Autschbach; Benjamin Funke; Felix Lasitschka; Nikolaus Gassler; Christine Fischer; Peter J Whorwell; Wendy Atkinson; Catherine Fell; Karl J Büchner; Marco Schmidtmann; Ivo van der Voort; Anna-Sophia Wisser; Thomas Berg; Gudrun Rappold; Beate Niesler
Journal:  Hum Mol Genet       Date:  2008-07-09       Impact factor: 6.150

6.  Mendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities.

Authors:  Jonathan J Lyons; Guangping Sun; Kelly D Stone; Celeste Nelson; Laura Wisch; Michelle O'Brien; Nina Jones; Andrew Lindsley; Hirsh D Komarow; Yun Bai; Linda M Scott; Daly Cantave; Irina Maric; J Pablo Abonia; Marc E Rothenberg; Lawrence B Schwartz; Joshua D Milner; Todd M Wilson
Journal:  J Allergy Clin Immunol       Date:  2014-01-25       Impact factor: 10.793

7.  Mutation in cytochrome b gene of mitochondrial DNA in a family with fibromyalgia is associated with NLRP3-inflammasome activation.

Authors:  Mario D Cordero; Elísabet Alcocer-Gómez; Fabiola Marín-Aguilar; Tatyana Rybkina; David Cotán; Antonio Pérez-Pulido; José Miguel Alvarez-Suarez; Maurizio Battino; José Antonio Sánchez-Alcazar; Angel M Carrión; Ognjen Culic; José M Navarro-Pando; Pedro Bullón
Journal:  J Med Genet       Date:  2015-11-13       Impact factor: 6.318

Review 8.  Ion channelopathies in functional GI disorders.

Authors:  Arthur Beyder; Gianrico Farrugia
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2016-08-11       Impact factor: 4.052

9.  Discovery of potential new gene variants and inflammatory cytokine associations with fibromyalgia syndrome by whole exome sequencing.

Authors:  Jinong Feng; Zhifang Zhang; Xiwei Wu; Allen Mao; Frances Chang; Xutao Deng; Harry Gao; Ching Ouyang; Kenneth J Dery; Keith Le; Jeffrey Longmate; Claudia Marek; R Paul St Amand; Theodore G Krontiris; John E Shively
Journal:  PLoS One       Date:  2013-06-10       Impact factor: 3.240
  9 in total

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