Works matching IS 00034800 AND DT 2018 AND VI 82 AND IP 2

Results: 11

Effectiveness of shrinkage and variable selection methods for the prediction of complex human traits using data from distantly related individuals.

Published in:: 2018
Publication type:: Correction Notice

Silenced DMBT1 promotes nasal mucosa epithelial cell growth.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 2, p. 102, doi. 10.1111/ahg.12230

By:

Lu, Xiaoqing;
Xu, Yaping;
Zhao, Yu;
Tao, Qilei;
Wu, Jian

Publication type:

Article

Fast permutation tests and related methods, for association between rare variants and binary outcomes.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 2, p. 93, doi. 10.1111/ahg.12229

By:

Sondhi, Arjun;
Rice, Kenneth Martin

Publication type:

Article

Recurrence of reported <italic>CDH23</italic> mutations causing DFNB12 in a special cohort of South Indian hearing impaired assortative mating families – an evaluation.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 2, p. 119, doi. 10.1111/ahg.12228

By:

Vanniya S, Paridhy;
Chandru, Jayasankaran;
Pavithra, Amritkumar;
Jeffrey, Justin Margret;
Kalaimathi, Murugesan;
Ramakrishnan, Rajagopalan;
Karthikeyen, Natarajan P.;
C. R. Srikumari, Srisailapathy

Publication type:

Article

The MOSAICC study: Assessing feasibility for biological sample collection in epidemiology studies and comparison of DNA yields from saliva and whole blood samples.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 2, p. 114, doi. 10.1111/ahg.12227

By:

James, Glen;
McMullin, Mary Frances;
Duncombe, Andrew S.;
Clarke, Mike;
Anderson, Lesley A.

Publication type:

Article

Exome sequence analysis and follow up genotyping implicates rare <italic>ULK1</italic> variants to be involved in susceptibility to schizophrenia.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 2, p. 88, doi. 10.1111/ahg.12226

By:

Al Eissa, Mariam M.;
Fiorentino, Alessia;
Sharp, Sally I.;
O'Brien, Niamh L.;
Wolfe, Kate;
Giaroli, Giovanni;
Curtis, David;
Bass, Nicholas J.;
McQuillin, Andrew

Publication type:

Article

A 3′ untranslated region polymorphism rs2304277 in the DNA repair pathway gene <italic>OGG1</italic> is a novel risk modulator for urothelial bladder carcinoma.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 2, p. 74, doi. 10.1111/ahg.12225

By:

Ahmed, Tayyaba;
Nawaz, Saira;
Noreen, Rabia;
Bangash, Kashif Sardar;
Rauf, Abdur;
Younis, Muhammad;
Anwar, Khursheed;
Khawaja, Muhammad Athar;
Azam, Maleeha;
Qureshi, Abid Ali;
Akhter, Saeed;
Kiemeney, Lambertus A.;
Qamar, Raheel;
Ali, Syeda Hafiza benish

Publication type:

Article

Parent‐of‐origin‐environment interactions in case‐parent triads with or without independent controls.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 2, p. 60, doi. 10.1111/ahg.12224

By:

Gjerdevik, Miriam;
Haaland, Øystein A.;
Romanowska, Julia;
Lie, Rolv T.;
Jugessur, Astanand;
Gjessing, Håkon K.

Publication type:

Article

Influence of <italic>Apolipoprotein E</italic> polymorphism on susceptibility of Wilson disease.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 2, p. 53, doi. 10.1111/ahg.12223

By:

Roy, Shubhrajit;
Ganguly, Kausik;
Pal, Prosenjit;
Ghosh, Sampurna;
Das, Shyamal K.;
Gangopadhyay, Prasanta K.;
Bavdekar, Ashish;
Ray, Kunal;
Sengupta, Mainak;
Ray, Jharna

Publication type:

Article

How many cases of disease in a pedigree imply familial disease?

Published in:

Annals of Human Genetics, 2018, v. 82, n. 2, p. 109, doi. 10.1111/ahg.12222

By:

Dudbridge, Frank;
Brown, Suzanne J.;
Ward, Lynley;
Wilson, Scott G.;
Walsh, John P.

Publication type:

Article

Issue Information.

Published in:: Annals of Human Genetics, 2018, v. 82, n. 2, p. 1, doi. 10.1111/ahg.12215
Publication type:: Article