Works matching DE "HUMAN variation (Biology)"

Results: 113

Genetic variability of micro RNA regulome in human.

Published in:

Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 1, p. 30, doi. 10.1002/mgg3.110

By:

Obsteter, Jana;
Dovc, Peter;
Kunej, Tanja

Publication type:

Article

No Association Between General Cognitive Ability and Rare Copy Number Variation.

Published in:

Behavior Genetics, 2013, v. 43, n. 3, p. 202, doi. 10.1007/s10519-013-9587-9

By:

McRae, Allan;
Wright, Margaret;
Hansell, Narelle;
Montgomery, Grant;
Martin, Nicholas

Publication type:

Article

THE NEED TO REIMAGINE DISABILITY RIGHTS LAW BECAUSE THE MEDICAL MODEL OF DISABILITY FAILS US ALL.

Published in:

Wisconsin Law Review, 2021, v. 2021, n. 2, p. 269

By:

GUEVARA, ANGÉLICA

Publication type:

Article

Human Genomic Deletions Generated by SVA-Associated Events.

Published in:

Comparative & Functional Genomics, 2012, p. 1, doi. 10.1155/2012/807270

By:

Jungnam Lee;
Jungsu Ha;
Son, Seung-Yeol;
Kyudong Han

Publication type:

Article

VARIATION IN HEIGHT AND BMI OF ADULT INDIANS.

Published in:

Journal of Biosocial Science, 2014, v. 46, n. 1, p. 47, doi. 10.1017/S002193201300014X

By:

SOM, SUPARNA;
ULIJASZEK, STANLEY;
PAL, MANORANJAN;
BHARATI, SUSMITA;
BHARATI, PREMANANDA

Publication type:

Article

ATTITUDES OF SERBIAN BIOLOGICAL ANTHROPOLOGISTS TOWARD THE CONCEPT OF RACE.

Published in:

Anthropologie, 2019, v. 57, n. 3, p. 287, doi. 10.26720/anthro.19.08.29.1

By:

ŠTRKALJ, GORAN;
BOŠKOVIĆ, ALEKSANDAR;
BUTUROVIĆ, ŽELJKA

Publication type:

Article

An integrated Asian human SNV and indel benchmark established using multiple sequencing methods.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66605-6

By:

Huang, Chuanfeng;
Shao, Libin;
Qu, Shoufang;
Rao, Junhua;
Cheng, Tao;
Cao, Zhisheng;
Liu, Sanyang;
Hu, Jie;
Liang, Xinming;
Shang, Ling;
Chen, Yangyi;
Liang, Zhikun;
Zhang, Jiezhong;
Chen, Peipei;
Luo, Donghong;
Zhu, Anna;
Yu, Ting;
Zhang, Wenxin;
Fan, Guangyi;
Chen, Fang

Publication type:

Article

Human evolutionary biology.

Published in:

2012

By:

Bowman, John

Publication type:

Book Review

Biological variation database: structure and criteria used for generation and update.

Published in:

Clinical Chemistry & Laboratory Medicine, 2015, v. 53, n. 2, p. 299, doi. 10.1515/cclm-2014-0739

By:

Perich, Carmen;
Minchinela, Joana;
Ricós, Carmen;
Fernández-Calle, Pilar;
Alvarez, Virtudes;
Doménech, María Vicenta;
Simón, Margarita;
Biosca, Carmen;
Boned, Beatriz;
García-Lario, José Vicente;
Cava, Fernando;
Fernández-Fernández, Pilar;
Fraser, Callum G.

Publication type:

Article

Gene bionetworks involved in the epigenetic transgenerational inheritance of altered mate preference: environmental epigenetics and evolutionary biology.

Published in:

BMC Genomics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2164-15-377

By:

Skinner, Michael K.;
Savenkova, Marina I.;
Bin Zhang;
Gore, Andrea C.;
Crews, David

Publication type:

Article

On the association of common and rare genetic variation influencing body mass index: a combined SNP and CNV analysis.

Published in:

BMC Genomics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2164-15-368

By:

Peterson, Roseann E.;
Maes, Hermine H.;
Peng Lin;
Kramer, John R.;
Hesselbrock, Victor M.;
Bauer, Lance O.;
Nurnberger Jr., John I.;
Edenberg, Howard J.;
Dick, Danielle M.;
Webb, Bradley T.

Publication type:

Article

Life Reveals Unkind Truths on its long Voyage.

Published in:

Poetcrit, 2023, v. 36, n. 2, p. 63, doi. 10.32381/POET.2023.36.02.8

By:

Prem, P. C. K.

Publication type:

Article

The accessible chromatin landscape of the human genome.

Published in:

Nature, 2012, v. 489, n. 7414, p. 75, doi. 10.1038/nature11232

By:

Thurman, Robert E.;
Rynes, Eric;
Humbert, Richard;
Vierstra, Jeff;
Maurano, Matthew T.;
Haugen, Eric;
Sheffield, Nathan C.;
Stergachis, Andrew B.;
Wang, Hao;
Vernot, Benjamin;
Garg, Kavita;
John, Sam;
Sandstrom, Richard;
Bates, Daniel;
Boatman, Lisa;
Canfield, Theresa K.;
Diegel, Morgan;
Dunn, Douglas;
Ebersol, Abigail K.;
Frum, Tristan

Publication type:

Article

Validated context-dependent associations of coronary heart disease risk with genotype variation in the chromosome 9p21 region: the Atherosclerosis Risk in Communities study.

Published in:

Human Genetics, 2014, v. 133, n. 9, p. 1105, doi. 10.1007/s00439-014-1451-3

By:

Lusk, Christine;
Dyson, Greg;
Clark, Andrew;
Ballantyne, Christie;
Frikke-Schmidt, Ruth;
Tybjærg-Hansen, Anne;
Boerwinkle, Eric;
Sing, Charles

Publication type:

Article

Recombination networks as genetic markers in a human variation study of the Old World.

Published in:

Human Genetics, 2012, v. 131, n. 4, p. 601, doi. 10.1007/s00439-011-1104-8

By:

Javed, Asif;
Melé, Marta;
Pybus, Marc;
Zalloua, Pierre;
Haber, Marc;
Comas, David;
Netea, Mihai;
Balanovsky, Oleg;
Balanovska, Elena;
Jin, Li;
Yang, Yajun;
ArunKumar, GaneshPrasad;
Pitchappan, Ramasamy;
Bertranpetit, Jaume;
Calafell, Francesc;
Parida, Laxmi

Publication type:

Article

Genetic variants in microRNA genes: impact on microRNA expression, function, and disease.

Published in:

Frontiers in Genetics, 2015, p. 1, doi. 10.3389/fgene.2015.00186

By:

Cammaerts, Sophia;
Strazisar, Mojca;
De Rijk, Peter;
Del Favero, Jurgen

Publication type:

Article

Genetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformation in hereditary hemorrhagic telangiectasia 1 (HHT1) and may influence expression of PTPN14.

Published in:

Frontiers in Genetics, 2015, v. 6, p. 1, doi. 10.3389/fgene.2015.00067

By:

Letteboer, Tom G. W.;
Benzinou, Michael;
Merrick, Christopher B.;
Quigley, David A.;
Kechen Zhau;
Kim, Il-Jin;
To, Minh D.;
Jablons, David M.;
van Amstel, Johannes K. P.;
Westermann, Cornelius J. J.;
Giraud, Sophie;
Dupuis-Girod, Sophie;
Lesca, Gaetan;
Berg, Jonathan H.;
Balmain, Allan;
Akhurst, Rosemary J.

Publication type:

Article

A symbiotic liaison between the genetic and epigenetic code.

Published in:

Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00113

By:

Heyn, Holger

Publication type:

Article

The advantages and challenges of neurodiversity employment in organizations.

Published in:

2019

By:

Krzeminska, Anna;
Austin, Robert D.;
Bruyère, Susanne M.;
Hedley, Darren

Publication type:

Editorial

Neural Dynamics Associated with Biological Variation in Normal Human Brain Regions.

Published in:

Entropy, 2024, v. 26, n. 10, p. 828, doi. 10.3390/e26100828

By:

Guisande, Natalí;
Rosso, Osvaldo A.;
Montani, Fernando

Publication type:

Article

Variations in DEPDC5 gene and its association with chronic hepatitis C virus infection in Saudi Arabia.

Published in:

BMC Infectious Diseases, 2014, v. 14, n. 1, p. 1, doi. 10.1186/s12879-014-0632-y

By:

Al-Anazi, Mashael R.;
Matou-Nasri, Sabine;
Abdo, Ayman A.;
Sanai, Faisal M.;
Khan, Mohammed Q.;
Albenmousa, Ali;
Al-Ashgar, Hamad I.;
Khalaf, Nisreen Z.;
Al-Ahdal, Mohammed N.;
Al-Qahtani, Ahmed A.

Publication type:

Article

Understanding Difference amid Superdiversity: Space, ‘Race’ and Granular Essentialisms at an Inner-City Football Club.

Published in:

Sociology, 2018, v. 52, n. 4, p. 639, doi. 10.1177/0038038516660039

By:

Rosbrook-Thompson, James

Publication type:

Article

The Littleness of Little Dorrit.

Published in:

Review of English Studies, 2023, v. 74, n. 316, p. 697, doi. 10.1093/res/hgad061

By:

Weltman, Sharon Aronofsky

Publication type:

Article

Identifying adaptive alleles in the human genome: from selection mapping to functional validation.

Published in:

Human Genetics, 2021, v. 140, n. 2, p. 241, doi. 10.1007/s00439-020-02206-7

By:

Werren, Elizabeth A.;
Garcia, Obed;
Bigham, Abigail W.

Publication type:

Article

Genome-wide scans reveal variants at EDAR predominantly affecting hair straightness in Han Chinese and Uyghur populations.

Published in:

Human Genetics, 2016, v. 135, n. 11, p. 1279, doi. 10.1007/s00439-016-1718-y

By:

Wu, Sijie;
Tan, Jingze;
Yang, Yajun;
Peng, Qianqian;
Zhang, Manfei;
Li, Jinxi;
Lu, Dongsheng;
Liu, Yu;
Lou, Haiyi;
Feng, Qidi;
Lu, Yan;
Guan, Yaqun;
Zhang, Zhaoxia;
Jiao, Yi;
Sabeti, Pardis;
Krutmann, Jean;
Tang, Kun;
Jin, Li;
Xu, Shuhua;
Wang, Sijia

Publication type:

Article

Discovery of mutations for Mendelian disorders.

Published in:

Human Genetics, 2016, v. 135, n. 6, p. 615, doi. 10.1007/s00439-016-1664-8

By:

Alkuraya, Fowzan

Publication type:

Article

Clinical genomics: from a truly personal genome viewpoint.

Published in:

Human Genetics, 2016, v. 135, n. 6, p. 591, doi. 10.1007/s00439-016-1682-6

By:

Lupski, James

Publication type:

Article

Admixture, Population Structure, and F-Statistics.

Published in:

Genetics, 2016, v. 202, n. 4, p. 1485, doi. 10.1534/genetics.115.183913

By:

Peter, Benjamin M.

Publication type:

Article

The Dynamics of Genetic Draft in Rapidly Adapting Populations.

Published in:

Genetics, 2013, v. 195, n. 3, p. 1007, doi. 10.1534/genetics.113.156430

By:

Kosheleva, Katya;
Desai, Michael M.

Publication type:

Article

Genetics and developmental biology of cooperation.

Published in:

Molecular Ecology, 2017, v. 26, n. 17, p. 4364, doi. 10.1111/mec.14208

By:

Kasper, Claudia;
Vierbuchen, Maddalena;
Ernst, Ulrich;
Fischer, Stefan;
Radersma, Reinder;
Raulo, Aura;
Cunha‐Saraiva, Filipa;
Wu, Min;
Mobley, Kenyon B.;
Taborsky, Barbara

Publication type:

Article

Using genetic variation to infer associations with climate in the common frog, Rana temporaria.

Published in:

Molecular Ecology, 2013, v. 22, n. 14, p. 3737, doi. 10.1111/mec.12334

By:

Muir, A. P.;
Thomas, R.;
Biek, R.;
Mable, B. K.

Publication type:

Article

Commentary on: Andrews SE, Roberts G, set P, Warburton F, Gilbert FJ. Third molar development in a London population of White British and black British or other Black ethnicity. J Forensic Sci. 2022;67(1):229–42. doi: 10.1111/1556‐4029.14928.

Published in:

Journal of Forensic Sciences, 2022, v. 67, n. 5, p. 2138, doi. 10.1111/1556-4029.15076

By:

Cervantes, Marianna;
Cardoso, Hugo F. V.

Publication type:

Article

The Devout and the Disabled: Religious and Cultural Accommodation‐as‐Human‐Variation.

Published in:

Journal of Applied Philosophy, 2018, v. 35, n. 4, p. 809, doi. 10.1111/japp.12267

By:

Zala, Miklos I.

Publication type:

Article

The sequencing and interpretation of the genome obtained from a Serbian individual.

Published in:

PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0208901

By:

Mohammed Ismail, Wazim;
Pagel, Kymberleigh A.;
Pejaver, Vikas;
Zhang, Simo V.;
Casasa, Sofia;
Mort, Matthew;
Cooper, David N.;
Hahn, Matthew W.;
Radivojac, Predrag

Publication type:

Article

Is Science Racist?

Published in:

2017

By:

Mncube, Zinhle

Publication type:

Book Review

Should a BRCA2 stop codon human variant, usually considered a polymorphism, be classified as a predisposing mutation?

Published in:

Cancer (0008543X), 2014, v. 120, n. 10, p. 1594, doi. 10.1002/cncr.28605

By:

D'Argenio, Valeria;
Esposito, Maria Valeria;
Gilder, Jean Ann;
Frisso, Giulia;
Salvatore, Francesco

Publication type:

Article

Next-generation-based targeted sequencing as an efficient tool for the study of the genetic background in Hirschsprung patients.

Published in:

BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0235-5

By:

Luzón-Toro, Berta;
Espino-Paisán, Laura;
Fernández, Raquel Ma.;
Martín-Sánchez, Marta;
Antiñolo, Guillermo;
Borrego, Salud

Publication type:

Article

Eye-color and Type-2 diabetes phenotype prediction from genotype data using deep learning methods.

Published in:

BMC Bioinformatics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12859-021-04077-9

By:

Muneeb, Muhammad;
Henschel, Andreas

Publication type:

Article

Eye-color and Type-2 diabetes phenotype prediction from genotype data using deep learning methods.

Published in:

BMC Bioinformatics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12859-021-04077-9

By:

Muneeb, Muhammad;
Henschel, Andreas

Publication type:

Article

Distinguishing functional polymorphism from random variation in the sequences of >10,000 HLA-A, -B and -C alleles.

Published in:

PLoS Genetics, 2017, v. 13, n. 6, p. 1, doi. 10.1371/journal.pgen.1006862

By:

Robinson, James;
Guethlein, Lisbeth A.;
Cereb, Nezih;
Yang, Soo Young;
Norman, Paul J.;
Marsh, Steven G. E.;
Parham, Peter

Publication type:

Article

Population genetic analysis of the DARC locus (Duffy) reveals adaptation from standing variation associated with malaria resistance in humans.

Published in:

PLoS Genetics, 2017, v. 13, n. 3, p. 1, doi. 10.1371/journal.pgen.1006560

By:

McManus, Kimberly F.;
Taravella, Angela M.;
Henn, Brenna M.;
Bustamante, Carlos D.;
Sikora, Martin;
Cornejo, Omar E.

Publication type:

Article

Alpha Helices Are More Robust to Mutations than Beta Strands.

Published in:

PLoS Computational Biology, 2016, v. 12, n. 12, p. 1, doi. 10.1371/journal.pcbi.1005242

By:

Abrusán, György;
Marsh, Joseph A.

Publication type:

Article

Geneticization in MIM/OMIM®? Exploring Historic and Epistemic Drivers of Contemporary Understandings of Genetic Disease.

Published in:

2017

By:

ANKENY, RACHEL A.

Publication type:

journal article

A Homogenizing Process of Selection Has Maintained an "Ultra-Slow" Acetylation NAT2 Variant in Humans.

Published in:

Human Biology, 2014, v. 86, n. 3, p. 185, doi. 10.13110/humanbiology.86.3.0185

By:

Patillon, B.;
Luisi, P.;
Poloni, E. S.;
Boukouvala, S.;
Darlu, P.;
Genin, E.;
Sabbagh, A.

Publication type:

Article

HLA Class II Alleles in the Otomi Population of the Mezquital Valley: A Genetic Approach to the History of Interethnic Migrations in the Mexican Central Plateau.

Published in:

Human Biology, 2014, v. 86, n. 3, p. 167, doi. 10.13110/humanbiology.86.3.0167

By:

Juárez-Martín, Ana Itzel;
González-Sobrino, Blanca Zoila;
Camarena Olvera, Ángel Eduardo;
Falfán-Valencia, Ramcés

Publication type:

Article

Interpreting polygenic scores, polygenic adaptation, and human phenotypic differences.

Published in:

Evolution, Medicine & Public Health, 2019, v. 2019, n. 1, p. 26, doi. 10.1093/emph/eoy036

By:

Rosenberg, Noah A;
Edge, Michael D;
Pritchard, Jonathan K;
Feldman, Marcus W

Publication type:

Article

Genomics Are Transforming Our Understanding of Responses to Climate Change.

Published in:

BioScience, 2015, v. 65, n. 3, p. 237, doi. 10.1093/biosci/biu219

By:

Stillman, Jonathon H.;
Armstrong, Eric

Publication type:

Article

Genetic variations of the FCER2 gene and asthma susceptibility in north Indian children: a case-control study.

Published in:

Biomarkers, 2013, v. 18, n. 8, p. 660, doi. 10.3109/1354750X.2013.840802

By:

Sharma, Neeraj;
Dixit, Pratibha;
Awasthi, Shally;
Phadke, Shubha R.

Publication type:

Article

Biological variation of high sensitivity cardiac troponin-T in stable dialysis patients: implications for clinical practice.

Published in:

Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 5, p. e147, doi. 10.1515/cclm-2015-0885

By:

Mbagaya, Wycliffe;
Luvai, Ahai

Publication type:

Article

The Body as a Substrate of Differentiation: Shifting the Focus from Race Science to Life Scientists' Research on Human Variation.

Published in:

Varia História, 2017, v. 33, n. 61, p. 109, doi. 10.1590/0104-87752017000100006

By:

Lipphardt, Veronika

Publication type:

Article