Literature DB >> 34478655

Response to Biesecker et al.

Ada Hamosh1, Joanna S Amberger2, Carol A Bocchini2, Joann Bodurtha2, Carol J Bult3, Christopher G Chute4, Garry R Cutting2, Harry C Dietz2, Helen V Firth5, Richard A Gibbs6, Wayne W Grody7, Melissa A Haendel8, James R Lupski9, Jennifer E Posey10, Peter N Robinson11, Lynn M Schriml12, Alan F Scott2, Nara L Sobreira2, David Valle2, Nan Wu13, Sonja A Rasmussen14.   

Abstract

Entities:  

Mesh:

Year:  2021        PMID: 34478655      PMCID: PMC8456153          DOI: 10.1016/j.ajhg.2021.07.004

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


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  9 in total

1.  TBX6 null variants and a common hypomorphic allele in congenital scoliosis.

Authors:  N Wu; X Ming; J Xiao; Z Wu; X Chen; M Shinawi; Y Shen; G Yu; J Liu; H Xie; Z S Gucev; S Liu; N Yang; H Al-Kateb; J Chen; J Zhang; N Hauser; T Zhang; V Tasic; P Liu; X Su; X Pan; C Liu; L Wang; J Shen; J Shen; Y Chen; T Zhang; J Zhang; K W Choy; J Wang; Q Wang; S Li; W Zhou; J Guo; Y Wang; C Zhang; Hong Zhao; Yu An; Yu Zhao; J Wang; Z Liu; Y Zuo; Y Tian; X Weng; V R Sutton; H Wang; Y Ming; S Kulkarni; T P Zhong; P F Giampietro; S L Dunwoodie; S W Cheung; X Zhang; L Jin; J R Lupski; G Qiu; F Zhang
Journal:  N Engl J Med       Date:  2015-01-07       Impact factor: 91.245

Review 2.  A dyadic approach to the delineation of diagnostic entities in clinical genomics.

Authors:  Leslie G Biesecker; Margaret P Adam; Fowzan S Alkuraya; Anne R Amemiya; Michael J Bamshad; Anita E Beck; James T Bennett; Lynne M Bird; John C Carey; Brian Chung; Robin D Clark; Timothy C Cox; Cynthia Curry; Mary Beth Palko Dinulos; William B Dobyns; Philip F Giampietro; Katta M Girisha; Ian A Glass; John M Graham; Karen W Gripp; Chad R Haldeman-Englert; Bryan D Hall; A Micheil Innes; Jennifer M Kalish; Kim M Keppler-Noreuil; Kenjiro Kosaki; Beth A Kozel; Ghayda M Mirzaa; John J Mulvihill; Malgorzata J M Nowaczyk; Roberta A Pagon; Kyle Retterer; Alan F Rope; Pedro A Sanchez-Lara; Laurie H Seaver; Joseph T Shieh; Anne M Slavotinek; Andrew K Sobering; Cathy A Stevens; David A Stevenson; Tiong Yang Tan; Wen-Hann Tan; Anne C Tsai; David D Weaver; Marc S Williams; Elaine Zackai; Yuri A Zarate
Journal:  Am J Hum Genet       Date:  2021-01-07       Impact factor: 11.025

3.  Annotating DNA variants is the next major goal for human genetics.

Authors:  Garry R Cutting
Journal:  Am J Hum Genet       Date:  2014-01-02       Impact factor: 11.025

Review 4.  Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice.

Authors:  C Castellani; H Cuppens; M Macek; J J Cassiman; E Kerem; P Durie; E Tullis; B M Assael; C Bombieri; A Brown; T Casals; M Claustres; G R Cutting; E Dequeker; J Dodge; I Doull; P Farrell; C Ferec; E Girodon; M Johannesson; B Kerem; M Knowles; A Munck; P F Pignatti; D Radojkovic; P Rizzotti; M Schwarz; M Stuhrmann; M Tzetis; J Zielenski; J S Elborn
Journal:  J Cyst Fibros       Date:  2008-05       Impact factor: 5.482

5.  Guidelines for human gene nomenclature.

Authors:  Elspeth A Bruford; Bryony Braschi; Paul Denny; Tamsin E M Jones; Ruth L Seal; Susan Tweedie
Journal:  Nat Genet       Date:  2020-08       Impact factor: 38.330

6.  Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation.

Authors:  Jennifer E Posey; Tamar Harel; Pengfei Liu; Jill A Rosenfeld; Regis A James; Zeynep H Coban Akdemir; Magdalena Walkiewicz; Weimin Bi; Rui Xiao; Yan Ding; Fan Xia; Arthur L Beaudet; Donna M Muzny; Richard A Gibbs; Eric Boerwinkle; Christine M Eng; V Reid Sutton; Chad A Shaw; Sharon E Plon; Yaping Yang; James R Lupski
Journal:  N Engl J Med       Date:  2016-12-07       Impact factor: 91.245

Review 7.  Insights into genetics, human biology and disease gleaned from family based genomic studies.

Authors:  Jennifer E Posey; Anne H O'Donnell-Luria; Jessica X Chong; Tamar Harel; Shalini N Jhangiani; Zeynep H Coban Akdemir; Steven Buyske; Davut Pehlivan; Claudia M B Carvalho; Samantha Baxter; Nara Sobreira; Pengfei Liu; Nan Wu; Jill A Rosenfeld; Sushant Kumar; Dimitri Avramopoulos; Janson J White; Kimberly F Doheny; P Dane Witmer; Corinne Boehm; V Reid Sutton; Donna M Muzny; Eric Boerwinkle; Murat Günel; Deborah A Nickerson; Shrikant Mane; Daniel G MacArthur; Richard A Gibbs; Ada Hamosh; Richard P Lifton; Tara C Matise; Heidi L Rehm; Mark Gerstein; Michael J Bamshad; David Valle; James R Lupski
Journal:  Genet Med       Date:  2019-01-18       Impact factor: 8.822

8.  Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Authors:  Sue Richards; Nazneen Aziz; Sherri Bale; David Bick; Soma Das; Julie Gastier-Foster; Wayne W Grody; Madhuri Hegde; Elaine Lyon; Elaine Spector; Karl Voelkerding; Heidi L Rehm
Journal:  Genet Med       Date:  2015-03-05       Impact factor: 8.822

9.  What's in a name? Issues to consider when naming Mendelian disorders.

Authors:  Sonja A Rasmussen; Ada Hamosh
Journal:  Genet Med       Date:  2020-06-18       Impact factor: 8.822

  9 in total
  1 in total

Review 1.  [Rare-disease data standards].

Authors:  Peter N Robinson; Holm Graessner
Journal:  Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz       Date:  2022-09-23       Impact factor: 1.595

  1 in total

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