Evaluation of Susceptibility Genes/Loci Associated with Male Androgenetic Alopecia (MAGA) for Female-Pattern Hair Loss in a Chinese Han Population and a Brief Literature Review.
Medical Science Monitor : International Medical Journal Of Experimental And Clinical Research
Liang, Bo B; Ding, Yantao Y; Zhou, Yi Y; Yang, Chunjun C; Cheng, Zhixiang Z
Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness.
Plos One
Hochfeld, Lara M LM; Bertolini, Marta M; Broadley, David D; Botchkareva, Natalia V NV; Betz, Regina C RC; Schoch, Susanne S; Nöthen, Markus M MM; Heilmann-Heimbach, Stefanie S
Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data.
Bmc Genomics
Pośpiech, Ewelina E; Kukla-Bartoszek, Magdalena M; Karłowska-Pik, Joanna J; Zieliński, Piotr P; Woźniak, Anna A; Boroń, Michał M; Dąbrowski, Michał M; Zubańska, Magdalena M; Jarosz, Agata A; Grzybowski, Tomasz T; Płoski, Rafał R; Spólnicka, Magdalena M; Branicki, Wojciech W
Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair.
Human Molecular Genetics
Liu, Fan F; Chen, Yan Y; Zhu, Gu G; Hysi, Pirro G PG; Wu, Sijie S; Adhikari, Kaustubh K; Breslin, Krystal K; Pospiech, Ewelina E; Hamer, Merel A MA; Peng, Fuduan F; Muralidharan, Charanya C; Acuna-Alonzo, Victor V; Canizales-Quinteros, Samuel S; Bedoya, Gabriel G; Gallo, Carla C; Poletti, Giovanni G; Rothhammer, Francisco F; Bortolini, Maria Catira MC; Gonzalez-Jose, Rolando R; Zeng, Changqing C; Xu, Shuhua S; Jin, Li L; Uitterlinden, André G AG; Ikram, M Arfan MA; van Duijn, Cornelia M CM; Nijsten, Tamar T; Walsh, Susan S; Branicki, Wojciech W; Wang, Sijia S; Ruiz-Linares, Andrés A; Spector, Timothy D TD; Martin, Nicholas G NG; Medland, Sarah E SE; Kayser, Manfred M
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
Nature Communications
Pirastu, Nicola N; Joshi, Peter K PK; de Vries, Paul S PS; Cornelis, Marilyn C MC; McKeigue, Paul M PM; Keum, NaNa N; Franceschini, Nora N; Colombo, Marco M; Giovannucci, Edward L EL; Spiliopoulou, Athina A; Franke, Lude L; North, Kari E KE; Kraft, Peter P; Morrison, Alanna C AC; Esko, Tõnu T; Wilson, James F JF
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.
Nature Communications
Heilmann-Heimbach, Stefanie S; Herold, Christine C; Hochfeld, Lara M LM; Hillmer, Axel M AM; Nyholt, Dale R DR; Hecker, Julian J; Javed, Asif A; Chew, Elaine G Y EG; Pechlivanis, Sonali S; Drichel, Dmitriy D; Heng, Xiu Ting XT; Del Rosario, Ricardo C-H RC; Fier, Heide L HL; Paus, Ralf R; Rueedi, Rico R; Galesloot, Tessel E TE; Moebus, Susanne S; Anhalt, Thomas T; Prabhakar, Shyam S; Li, Rui R; Kanoni, Stavroula S; Papanikolaou, George G; Kutalik, Zoltán Z; Deloukas, Panos P; Philpott, Michael P MP; Waeber, Gérard G; Spector, Tim D TD; Vollenweider, Peter P; Kiemeney, Lambertus A L M LA; Dedoussis, George G; Richards, J Brent JB; Nothnagel, Michael M; Martin, Nicholas G NG; Becker, Tim T; Hinds, David A DA; Nöthen, Markus M MM
Expression profiling and bioinformatic analyses suggest new target genes and pathways for human hair follicle related microRNAs.
Bmc Dermatology
Hochfeld, Lara M LM; Anhalt, Thomas T; Reinbold, Céline S CS; Herrera-Rivero, Marisol M; Fricker, Nadine N; Nöthen, Markus M MM; Heilmann-Heimbach, Stefanie S
Prediction of male-pattern baldness from genotypes.
European Journal Of Human Genetics : Ejhg
Liu, Fan F; Hamer, Merel A MA; Heilmann, Stefanie S; Herold, Christine C; Moebus, Susanne S; Hofman, Albert A; Uitterlinden, André G AG; Nöthen, Markus M MM; van Duijn, Cornelia M CM; Nijsten, Tamar Ec TE; Kayser, Manfred M
Evaluation of DNA variants associated with androgenetic alopecia and their potential to predict male pattern baldness.
Plos One
Marcińska, Magdalena M; Pośpiech, Ewelina E; Abidi, Sarah S; Andersen, Jeppe Dyrberg JD; van den Berge, Margreet M; Carracedo, Ángel Á; Eduardoff, Mayra M; Marczakiewicz-Lustig, Anna A; Morling, Niels N; Sijen, Titia T; Skowron, Małgorzata M; Söchtig, Jens J; Syndercombe-Court, Denise D; Weiler, Natalie N; , ; Schneider, Peter M PM; Ballard, David D; Børsting, Claus C; Parson, Walther W; Phillips, Chris C; Branicki, Wojciech W
Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.
Plos One
Arte, Sirpa S; Parmanen, Satu S; Pirinen, Sinikka S; Alaluusua, Satu S; Nieminen, Pekka P
Haplotype association analysis of genes within the WNT signalling pathways in diabetic nephropathy.
Bmc Nephrology
Kavanagh, David H DH; Savage, David A DA; Patterson, Christopher C CC; McKnight, Amy Jayne AJ; Crean, John K JK; Maxwell, Alexander P AP; McKay, Gareth J GJ; ,
Polymorphisms in WNT6 and WNT10A and colorectal adenoma risk.
Nutrition And Cancer
Galbraith, Rachel L RL; Poole, Elizabeth M EM; Duggan, David D; Muehling, Jill J; Hsu, Li L; Makar, Karen K; Xiao, Liren L; Potter, John D JD; Ulrich, Cornelia M CM
Web-based, participant-driven studies yield novel genetic associations for common traits.
Plos Genetics
Eriksson, Nicholas N; Macpherson, J Michael JM; Tung, Joyce Y JY; Hon, Lawrence S LS; Naughton, Brian B; Saxonov, Serge S; Avey, Linda L; Wojcicki, Anne A; Pe'er, Itsik I; Mountain, Joanna J
Common variants in the trichohyalin gene are associated with straight hair in Europeans.
American Journal Of Human Genetics
Medland, Sarah E SE; Nyholt, Dale R DR; Painter, Jodie N JN; McEvoy, Brian P BP; McRae, Allan F AF; Zhu, Gu G; Gordon, Scott D SD; Ferreira, Manuel A R MA; Wright, Margaret J MJ; Henders, Anjali K AK; Campbell, Megan J MJ; Duffy, David L DL; Hansell, Narelle K NK; Macgregor, Stuart S; Slutske, Wendy S WS; Heath, Andrew C AC; Montgomery, Grant W GW; Martin, Nicholas G NG