PCSK1 c.661A>G ;(p.N221D)

Variant ID: 5-95751785-T-C

NM_000439.4(PCSK1):c.661A>G;(p.N221D)

This variant was identified in 77 publications

View GRCh38 version.




Publications:


Workflow enabling deepscale immunopeptidome, proteome, ubiquitylome, phosphoproteome, and acetylome analyses of sample-limited tissues.

Nature Communications
Abelin, Jennifer G JG; Bergstrom, Erik J EJ; Rivera, Keith D KD; Taylor, Hannah B HB; Klaeger, Susan S; Xu, Charles C; Verzani, Eva K EK; Jackson White, C C; Woldemichael, Hilina B HB; Virshup, Maya M; Olive, Meagan E ME; Maynard, Myranda M; Vartany, Stephanie A SA; Allen, Joseph D JD; Phulphagar, Kshiti K; Harry Kane, M M; Rachimi, Suzanna S; Mani, D R DR; Gillette, Michael A MA; Satpathy, Shankha S; Clauser, Karl R KR; Udeshi, Namrata D ND; Carr, Steven A SA
Publication Date: 2023-04-03

Variant appearance in text: PCSK1: N221D
PubMed Link: 37012232
Variant Present in the following documents:
  • 41467_2023_37547_MOESM12_ESM.xlsx, sheet 3
  • 41467_2023_37547_MOESM12_ESM.xlsx, sheet 2
View BVdb publication page



Clinical assessment for diet prescription.

Journal Of Preventive Medicine And Hygiene
Kiani, Aysha Karim AK; Medori, Maria Chiara MC; Dhuli, Kristjana K; Donato, Kevin K; Caruso, Paola P; Fioretti, Francesco F; Perrone, Marco Alfonso MA; Ceccarini, Maria Rachele MR; Manganotti, Paolo P; Nodari, Savina S; Codini, Michela M; Beccari, Tommaso T; Bertelli, Matteo M
Publication Date: 2022-06

Variant appearance in text: rs6232
PubMed Link: 36479490
Variant Present in the following documents:
  • Main text
  • jpmh-2022-02-e102.pdf
View BVdb publication page



Modulation of PC1/3 activity by a rare double-site homozygous mutation.

Frontiers In Pediatrics
Ni, Yanyan Y; Chen, Xiangxiang X; Sun, Yi Y; Pan, Jiarong J; Tang, Chao C; Yuan, Tianming T
Publication Date: 2022

Variant appearance in text: rs6232
PubMed Link: 36389395
Variant Present in the following documents:
  • Main text
  • fped-10-1026707.pdf
View BVdb publication page



Association between SNPs in Leptin Pathway Genes and Anthropometric, Biochemical, and Dietary Markers Related to Obesity.

Genes
Cadena-López, Ricardo Omar RO; Hernández-Rodríguez, Lourdes Vanessa LV; Aguilar-Galarza, Adriana A; García-Muñoz, Willebaldo W; Haddad-Talancón, Lorenza L; Anzures-Cortes, Ma de Lourdes ML; Velázquez-Sánchez, Claudia C; Flores-Viveros, Karla Lucero KL; Anaya-Loyola, Miriam Aracely MA; García-Gasca, Teresa T; Rodríguez-García, Víctor Manuel VM; Moreno-Celis, Ulisses U
Publication Date: 2022-05-25

Variant appearance in text: rs6232
PubMed Link: 35741707
Variant Present in the following documents:
  • Main text
  • genes-13-00945.pdf
View BVdb publication page



Testing for rare genetic causes of obesity: findings and experiences from a pediatric weight management program.

International Journal Of Obesity (2005)
Roberts, Karyn J KJ; Ariza, Adolfo J AJ; Selvaraj, Kavitha K; Quadri, Maheen M; Mangarelli, Caren C; Neault, Sarah S; Davis, Erica E EE; Binns, Helen J HJ
Publication Date: 2022-08

Variant appearance in text: rs6232
PubMed Link: 35562395
Variant Present in the following documents:
  • 41366_2022_Article_1139.pdf
View BVdb publication page



Comparative Analyses of Turkish Variome and Widely Used Genomic Variation Databases for the Evaluation of Rare Sequence Variants in Turkish Individuals: Idiopathic Hypogonadotropic Hypogonadism as a Disease Model

Journal Of Clinical Research In Pediatric Endocrinology
Kotan, Leman Damla LD
Publication Date: 2022-08-25

Variant appearance in text: rs6232
PubMed Link: 35438269
Variant Present in the following documents:
  • JCRPE-14-293.pdf
View BVdb publication page



Obesity, POMC, and POMC-processing Enzymes: Surprising Results From Animal Models.

Endocrinology
Lindberg, Iris I; Fricker, Lloyd D LD
Publication Date: 2021-12-01

Variant appearance in text: PC1/3: N221D
PubMed Link: 34333593
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of Genetic Variants in 65 Obesity Related Genes in a Cohort of Portuguese Obese Individuals.

Genes
Ginete, Catarina C; Serrasqueiro, Bernardo B; Silva-Nunes, José J; Veiga, Luísa L; Brito, Miguel M
Publication Date: 2021-04-19

Variant appearance in text: rs6232
PubMed Link: 33921825
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mouse Models of Human Proprotein Convertase Insufficiency.

Endocrine Reviews
Shakya, Manita M; Lindberg, Iris I
Publication Date: 2021-05-25

Variant appearance in text: PC1/3: N221D; rs6232
PubMed Link: 33382413
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic test for the prescription of diets in support of physical activity.

Acta Bio-Medica : Atenei Parmensis
Naureen, Zakira Z; Miggiano, Giacinto Abele Donato GAD; Aquilanti, Barbara B; Velluti, Valeria V; Matera, Giuseppina G; Gagliardi, Lucilla L; Zulian, Alessandra A; Romanelli, Roberta R; Bertelli, Matteo M
Publication Date: 2020-11-09

Variant appearance in text: rs6232
PubMed Link: 33170161
Variant Present in the following documents:
  • Main text
  • ACTA-91-11.pdf
View BVdb publication page



Reduced Stability and pH-Dependent Activity of a Common Obesity-Linked PCSK1 Polymorphism, N221D.

Endocrinology
Jarvela, Timothy S TS; Shakya, Manita M; Bachor, Tomas T; White, Anne A; Low, Malcolm J MJ; Lindberg, Iris I
Publication Date: 2019-11-01

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 31504391
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sexual Dimorphism of a Genetic Risk Score for Obesity and Related Traits among Chinese Patients with Type 2 Diabetes.

Obesity Facts
Kong, Xiaomu X; Xing, Xiaoyan X; Zhang, Xuelian X; Hong, Jing J; Yang, Wenying W
Publication Date: 2019

Variant appearance in text: rs6232
PubMed Link: 31167208
Variant Present in the following documents:
  • Main text
View BVdb publication page



Congenital Leptin Deficiency and Leptin Gene Missense Mutation Found in Two Colombian Sisters with Severe Obesity.

Genes
Yupanqui-Lozno, Hernan H; Bastarrachea, Raul A RA; Yupanqui-Velazco, Maria E ME; Alvarez-Jaramillo, Monica M; Medina-Méndez, Esteban E; Giraldo-Peña, Aida P AP; Arias-Serrano, Alexandra A; Torres-Forero, Carolina C; Garcia-Ordoñez, Angelica M AM; Mastronardi, Claudio A CA; Restrepo, Carlos M CM; Rodriguez-Ayala, Ernesto E; Nava-Gonzalez, Edna J EJ; Arcos-Burgos, Mauricio M; Kent, Jack W JW; Cole, Shelley A SA; Licinio, Julio J; Celis-Regalado, Luis G LG
Publication Date: 2019-05-07

Variant appearance in text: PCSK1: 661A>G
PubMed Link: 31067764
Variant Present in the following documents:
  • Main text
  • genes-10-00342.pdf
View BVdb publication page



Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics.

Scientific Reports
John, Sumi Elsa SE; Antony, Dinu D; Eaaswarkhanth, Muthukrishnan M; Hebbar, Prashantha P; Channanath, Arshad Mohamed AM; Thomas, Daisy D; Devarajan, Sriraman S; Tuomilehto, Jaakko J; Al-Mulla, Fahd F; Alsmadi, Osama O; Thanaraj, Thangavel Alphonse TA
Publication Date: 2018-11-08

Variant appearance in text: rs6232
PubMed Link: 30409984
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_34815.pdf
View BVdb publication page



Melanocortin 4 Receptor Pathway Dysfunction in Obesity: Patient Stratification Aimed at MC4R Agonist Treatment.

The Journal Of Clinical Endocrinology And Metabolism
Ayers, Kristin L KL; Glicksberg, Benjamin S BS; Garfield, Alastair S AS; Longerich, Simonne S; White, Joseph A JA; Yang, Pengwei P; Du, Lei L; Chittenden, Thomas W TW; Gulcher, Jeffery R JR; Roy, Sophie S; Fiedorek, Fred F; Gottesdiener, Keith K; Cohen, Sarah S; North, Kari E KE; Schadt, Eric E EE; Li, Shuyu D SD; Chen, Rong R; Van der Ploeg, Lex H T LHT
Publication Date: 2018-07-01

Variant appearance in text: PC1: 661A>G; rs6232
PubMed Link: 29726959
Variant Present in the following documents:
  • Main text
  • jc.2018-00258.st1.xlsx, sheet 4
  • jc.2018-00258.st1.xlsx, sheet 3
  • jc.2018-00258.sd1.pdf
View BVdb publication page



Interactions between Genetics and Sugar-Sweetened Beverage Consumption on Health Outcomes: A Review of Gene-Diet Interaction Studies.

Frontiers In Endocrinology
Haslam, Danielle E DE; McKeown, Nicola M NM; Herman, Mark A MA; Lichtenstein, Alice H AH; Dashti, Hassan S HS
Publication Date: 2017

Variant appearance in text: rs6232
PubMed Link: 29375475
Variant Present in the following documents:
  • Main text
  • fendo-08-00368.pdf
View BVdb publication page



Role of MMP-1 (-519A/G, -1607 1G/2G), MMP-3 (Lys45Glu), MMP-7 (-181A/G), and MMP-12 (-82A/G) Variants and Plasma MMP Levels on Obesity-Related Phenotypes and Microvascular Reactivity in a Tunisian Population.

Disease Markers
Boumiza, Soumaya S; Bchir, Sarra S; Ben Nasr, Hela H; Abbassi, Ammar A; Jacob, Marie-Paule MP; Norel, Xavier X; Tabka, Zouhair Z; Chahed, Karim K
Publication Date: 2017

Variant appearance in text: rs6232
PubMed Link: 29317790
Variant Present in the following documents:
  • Main text
  • DM2017-6198526.pdf
View BVdb publication page



Development and validation of a targeted next generation DNA sequencing panel outperforming whole exome sequencing for the identification of clinically relevant genetic variants.

Oncotarget
Miller, Eirwen M EM; Patterson, Nicole E NE; Zechmeister, Jenna Marcus JM; Bejerano-Sagie, Michal M; Delio, Maria M; Patel, Kunjan K; Ravi, Nivedita N; Quispe-Tintaya, Wilber W; Maslov, Alexander A; Simmons, Nichelle N; Castaldi, Maria M; Vijg, Jan J; Karabakhtsian, Rouzan G RG; Greally, John M JM; Kuo, Dennis Y S DYS; Montagna, Cristina C
Publication Date: 2017-11-24

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 29254223
Variant Present in the following documents:
  • oncotarget-08-102033-s003.xlsx, sheet 1
View BVdb publication page



Penetrance of Polygenic Obesity Susceptibility Loci across the Body Mass Index Distribution.

American Journal Of Human Genetics
Abadi, Arkan A; Alyass, Akram A; Robiou du Pont, Sebastien S; Bolker, Ben B; Singh, Pardeep P; Mohan, Viswanathan V; Diaz, Rafael R; Engert, James C JC; Yusuf, Salim S; Gerstein, Hertzel C HC; Anand, Sonia S SS; Meyre, David D
Publication Date: 2017-12-07

Variant appearance in text: rs6232
PubMed Link: 29220676
Variant Present in the following documents:
  • Main text
View BVdb publication page



Functional analysis of PCSK2 coding variants: A founder effect in the Old Order Amish population.

Diabetes Research And Clinical Practice
Winters, Alexandra A; Ramos-Molina, Bruno B; Jarvela, Timothy S TS; Yerges-Armstrong, Laura L; Pollin, Toni I TI; Lindberg, Iris I
Publication Date: 2017-09

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 28719828
Variant Present in the following documents:
  • Main text
View BVdb publication page



Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.

Scientific Reports
Chen, Xiaowei Sylvia XS; Reader, Rose H RH; Hoischen, Alexander A; Veltman, Joris A JA; Simpson, Nuala H NH; Francks, Clyde C; Newbury, Dianne F DF; Fisher, Simon E SE
Publication Date: 2017-04-25

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 28440294
Variant Present in the following documents:
  • srep46105-s2.xls, sheet 9
View BVdb publication page



Functional and clinical relevance of novel and known PCSK1 variants for childhood obesity and glucose metabolism.

Molecular Metabolism
Löffler, Dennis D; Behrendt, Susanne S; Creemers, John W M JWM; Klammt, Jürgen J; Aust, Gabriela G; Stanik, Juraj J; Kiess, Wieland W; Kovacs, Peter P; Körner, Antje A
Publication Date: 2017-03

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 28271036
Variant Present in the following documents:
  • Main text
View BVdb publication page



The New Immortalized Uroepithelial Cell Line HBLAK Contains Defined Genetic Aberrations Typical of Early Stage Urothelial Tumors.

Bladder Cancer (Amsterdam, Netherlands)
Hoffmann, Michèle J MJ; Koutsogiannouli, Evangelia E; Skowron, Margaretha A MA; Pinkerneil, Maria M; Niegisch, Günter G; Brandt, Artur A; Stepanow, Stefanie S; Rieder, Harald H; Schulz, Wolfgang A WA
Publication Date: 2016-10-27

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 28035326
Variant Present in the following documents:
  • blc-2-blc160065-s001.xlsx, sheet 2
View BVdb publication page



Association of genetic variants of the incretin-related genes with quantitative traits and occurrence of type 2 diabetes in Japanese.

Molecular Genetics And Metabolism Reports
Enya, Mayumi M; Horikawa, Yukio Y; Iizuka, Katsumi K; Takeda, Jun J
Publication Date: 2014

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 27896108
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



The importance of gene-environment interactions in human obesity.

Clinical Science (London, England : 1979)
Reddon, Hudson H; Guéant, Jean-Louis JL; Meyre, David D
Publication Date: 2016-09-01

Variant appearance in text: rs6232
PubMed Link: 27503943
Variant Present in the following documents:
  • Main text
View BVdb publication page



Longitudinal relationships between glycemic status and body mass index in a multiethnic study: evidence from observational and genetic epidemiology.

Scientific Reports
Ishola, Adeola F AF; Gerstein, Hertzel C HC; Engert, James C JC; Mohan, Viswanathan V; Diaz, Rafael R; Anand, Sonia S SS; Meyre, David D
Publication Date: 2016-08-02

Variant appearance in text: rs6232
PubMed Link: 27480816
Variant Present in the following documents:
  • Main text
  • srep30744.pdf
View BVdb publication page



PCSK1 Variants and Human Obesity.

Progress In Molecular Biology And Translational Science
Ramos-Molina, B B; Martin, M G MG; Lindberg, I I
Publication Date: 2016

Variant appearance in text: PC1/3: N221D; rs6232
PubMed Link: 27288825
Variant Present in the following documents:
  • Main text
View BVdb publication page



Molecular analysis of urothelial cancer cell lines for modeling tumor biology and drug response.

Oncogene
Nickerson, M L ML; Witte, N N; Im, K M KM; Turan, S S; Owens, C C; Misner, K K; Tsang, S X SX; Cai, Z Z; Wu, S S; Dean, M M; Costello, J C JC; Theodorescu, D D
Publication Date: 2017-01-05

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 27270441
Variant Present in the following documents:
  • onc2016172x3.xls, sheet 3
View BVdb publication page



Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study.

Scientific Reports
Reddon, Hudson H; Gerstein, Hertzel C HC; Engert, James C JC; Mohan, Viswanathan V; Bosch, Jackie J; Desai, Dipika D; Bailey, Swneke D SD; Diaz, Rafael R; Yusuf, Salim S; Anand, Sonia S SS; Meyre, David D
Publication Date: 2016-01-04

Variant appearance in text: rs6232
PubMed Link: 26727462
Variant Present in the following documents:
  • Main text
  • srep18672.pdf
View BVdb publication page



Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015

Variant appearance in text: PC1: N221D; rs6232
PubMed Link: 26659599
Variant Present in the following documents:
  • pone.0144692.s002.xlsx, sheet 1
View BVdb publication page



Revisiting PC1/3 Mutants: Dominant-Negative Effect of Endoplasmic Reticulum-Retained Mutants.

Endocrinology
Blanco, Elias H EH; Ramos-Molina, Bruno B; Lindberg, Iris I
Publication Date: 2015-10

Variant appearance in text: PC1/3: N221D; rs6232
PubMed Link: 26207343
Variant Present in the following documents:
  • Main text
View BVdb publication page



GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25

Variant appearance in text: PCSK1: N221D
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 3
View BVdb publication page



Whole-exome sequencing of primary plasma cell leukemia discloses heterogeneous mutational patterns.

Oncotarget
Cifola, Ingrid I; Lionetti, Marta M; Pinatel, Eva E; Todoerti, Katia K; Mangano, Eleonora E; Pietrelli, Alessandro A; Fabris, Sonia S; Mosca, Laura L; Simeon, Vittorio V; Petrucci, Maria Teresa MT; Morabito, Fortunato F; Offidani, Massimo M; Di Raimondo, Francesco F; Falcone, Antonietta A; Caravita, Tommaso T; Battaglia, Cristina C; De Bellis, Gianluca G; Palumbo, Antonio A; Musto, Pellegrino P; Neri, Antonino A
Publication Date: 2015-07-10

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 26046463
Variant Present in the following documents:
  • oncotarget-06-17543-s002.xls, sheet 1
View BVdb publication page



22nd European Congress on Obesity (ECO2015), Prague, Czech Republic, May 6-9, 2015: Abstracts.

Obesity Facts
Publication Date: 2015

Variant appearance in text: rs6232
PubMed Link: 25969149
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphisms of the peroxisome proliferator-activated receptor-γ (rs1801282) and its coactivator-1 (rs8192673) are associated with obesity indexes in subjects with type 2 diabetes mellitus.

Cardiovascular Diabetology
Kruzliak, Peter P; Haley, Andreana P AP; Starcevic, Jovana Nikolajevic JN; Gaspar, Ludovit L; Petrovic, Daniel D
Publication Date: 2015-04-28

Variant appearance in text: rs6232
PubMed Link: 25928419
Variant Present in the following documents:
  • Main text
  • 12933_2015_Article_197.pdf
View BVdb publication page



Whole-exome sequencing of pancreatic cancer defines genetic diversity and therapeutic targets.

Nature Communications
Witkiewicz, Agnieszka K AK; McMillan, Elizabeth A EA; Balaji, Uthra U; Baek, GuemHee G; Lin, Wan-Chi WC; Mansour, John J; Mollaee, Mehri M; Wagner, Kay-Uwe KU; Koduru, Prasad P; Yopp, Adam A; Choti, Michael A MA; Yeo, Charles J CJ; McCue, Peter P; White, Michael A MA; Knudsen, Erik S ES
Publication Date: 2015-04-09

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 25855536
Variant Present in the following documents:
  • ncomms7744-s2.xlsx, sheet 1
View BVdb publication page



Obesity genetics in mouse and human: back and forth, and back again.

Peerj
Yazdi, Fereshteh T FT; Clee, Susanne M SM; Meyre, David D
Publication Date: 2015

Variant appearance in text: rs6232
PubMed Link: 25825681
Variant Present in the following documents:
  • Main text
View BVdb publication page



Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals.

Human Molecular Genetics
Nead, Kevin T KT; Li, Aihua A; Wehner, Mackenzie R MR; Neupane, Binod B; Gustafsson, Stefan S; Butterworth, Adam A; Engert, James C JC; Davis, A Darlene AD; Hegele, Robert A RA; Miller, Ruby R; den Hoed, Marcel M; Khaw, Kay-Tee KT; Kilpeläinen, Tuomas O TO; Wareham, Nick N; Edwards, Todd L TL; Hallmans, Göran G; Varga, Tibor V TV; Kardia, Sharon L R SL; Smith, Jennifer A JA; Zhao, Wei W; Faul, Jessica D JD; Weir, David D; Mi, Jie J; Xi, Bo B; Quinteros, Samuel Canizales SC; Cooper, Cyrus C; Sayer, Avan Aihie AA; Jameson, Karen K; Grøntved, Anders A; Fornage, Myriam M; Sidney, Stephen S; Hanis, Craig L CL; Highland, Heather M HM; Häring, Hans-Ulrich HU; Heni, Martin M; Lasky-Su, Jessica J; Weiss, Scott T ST; Gerhard, Glenn S GS; Still, Christopher C; Melka, Melkaey M MM; Pausova, Zdenka Z; Paus, Tomáš T; Grant, Struan F A SF; Hakonarson, Hakon H; Price, R Arlen RA; Wang, Kai K; Scherag, Andre A; Hebebrand, Johannes J; Hinney, Anke A; , ; Franks, Paul W PW; Frayling, Timothy M TM; McCarthy, Mark I MI; Hirschhorn, Joel N JN; Loos, Ruth J RJ; Ingelsson, Erik E; Gerstein, Hertzel C HC; Yusuf, Salim S; Beyene, Joseph J; Anand, Sonia S SS; Meyre, David D
Publication Date: 2015-06-15

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 25784503
Variant Present in the following documents:
  • Main text
View BVdb publication page



Whole exome sequencing of a single osteosarcoma case--integrative analysis with whole transcriptome RNA-seq data.

Human Genomics
Reimann, Ene E; Kõks, Sulev S; Ho, Xuan Dung XD; Maasalu, Katre K; Märtson, Aare A
Publication Date: 2014-12-11

Variant appearance in text: PCSK1: N221D
PubMed Link: 25496518
Variant Present in the following documents:
  • 40246_2014_20_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Replication of obesity and diabetes-related SNP associations in individuals from Yucatán, México.

Frontiers In Genetics
Hernandez-Escalante, Victor M VM; Nava-Gonzalez, Edna J EJ; Voruganti, V Saroja VS; Kent, Jack W JW; Haack, Karin K; Laviada-Molina, Hugo A HA; Molina-Segui, Fernanda F; Gallegos-Cabriales, Esther C EC; Lopez-Alvarenga, Juan Carlos JC; Cole, Shelley A SA; Mezzles, Marguerite J MJ; Comuzzie, Anthony G AG; Bastarrachea, Raul A RA
Publication Date: 2014

Variant appearance in text: rs6232
PubMed Link: 25477898
Variant Present in the following documents:
  • Main text
  • fgene-05-00380.pdf
View BVdb publication page



Whole-genome sequencing of the world's oldest people.

Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 25390934
Variant Present in the following documents:
  • pone.0112430.s004.xlsx, sheet 1
View BVdb publication page



Obesity-related genomic loci are associated with type 2 diabetes in a Han Chinese population.

Plos One
Kong, Xiaomu X; Zhang, Xuelian X; Zhao, Qi Q; He, Jiang J; Chen, Li L; Zhao, Zhigang Z; Li, Qiang Q; Ge, Jiapu J; Chen, Gang G; Guo, Xiaohui X; Lu, Juming J; Weng, Jianping J; Jia, Weiping W; Ji, Linong L; Xiao, Jianzhong J; Shan, Zhongyan Z; Liu, Jie J; Tian, Haoming H; Ji, Qiuhe Q; Zhu, Dalong D; Zhou, Zhiguang Z; Shan, Guangliang G; Yang, Wenying W
Publication Date: 2014

Variant appearance in text: rs6232
PubMed Link: 25093408
Variant Present in the following documents:
  • Main text
View BVdb publication page



NCI-60 whole exome sequencing and pharmacological CellMiner analyses.

Plos One
Reinhold, William C WC; Varma, Sudhir S; Sousa, Fabricio F; Sunshine, Margot M; Abaan, Ogan D OD; Davis, Sean R SR; Reinhold, Spencer W SW; Kohn, Kurt W KW; Morris, Joel J; Meltzer, Paul S PS; Doroshow, James H JH; Pommier, Yves Y
Publication Date: 2014

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 25032700
Variant Present in the following documents:
  • pone.0101670.s004.xlsx, sheet 1
View BVdb publication page



Abstracts of the 21th European Congress on Obesity (ECO2014), May 28-31, 2014, Sofia, Bulgaria.

Obesity Facts
Publication Date: 2014

Variant appearance in text: rs6232
PubMed Link: 24860936
Variant Present in the following documents:
  • Main text
  • ofa-0007-0001.pdf
View BVdb publication page



Defective transport of the obesity mutant PC1/3 N222D contributes to loss of function.

Endocrinology
Prabhu, Yogikala Y; Blanco, Elias H EH; Liu, Ming M; Peinado, Juan R JR; Wheeler, Matthew C MC; Gekakis, Nicholas N; Arvan, Peter P; Lindberg, Iris I
Publication Date: 2014-07

Variant appearance in text: PC1/3: N221D; rs6232
PubMed Link: 24828610
Variant Present in the following documents:
  • Main text
View BVdb publication page



Meta-analyses between 18 candidate genetic markers and overweight/obesity.

Diagnostic Pathology
Tang, Linlin L; Ye, Huadan H; Hong, Qingxiao Q; Chen, Fei F; Wang, Qinwen Q; Xu, Leiting L; Bu, Shizhong S; Liu, Qiong Q; Ye, Meng M; Wang, Dao Wen DW; Mai, Yifeng Y; Duan, Shiwei S
Publication Date: 2014-03-12

Variant appearance in text: rs6232
PubMed Link: 24621099
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variants in PCSK1 gene are associated with the risk of coronary artery disease in type 2 diabetes in a Chinese Han population: a case control study.

Plos One
Wei, Xiaowei X; Ma, Xiaowei X; Lu, Ran R; Bai, Ge G; Zhang, Jianwei J; Deng, Ruifen R; Gu, Nan N; Feng, Nan N; Guo, Xiaohui X
Publication Date: 2014

Variant appearance in text: rs6232
PubMed Link: 24489861
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Genetics of the first seven proprotein convertase enzymes in health and disease.

Current Genomics
Turpeinen, Hannu H; Ortutay, Zsuzsanna Z; Pesu, Marko M
Publication Date: 2013-11

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 24396277
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Exome sequencing finds a novel PCSK1 mutation in a child with generalized malabsorptive diarrhea and diabetes insipidus.

Journal Of Pediatric Gastroenterology And Nutrition
Yourshaw, Michael M; Solorzano-Vargas, R Sergio RS; Pickett, Lindsay A LA; Lindberg, Iris I; Wang, Jiafang J; Cortina, Galen G; Pawlikowska-Haddal, Anna A; Baron, Howard H; Venick, Robert S RS; Nelson, Stanley F SF; Martín, Martín G MG
Publication Date: 2013-12

Variant appearance in text: PCSK1: N221D
PubMed Link: 24280991
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Proprotein convertases in high-density lipoprotein metabolism.

Biomarker Research
Choi, Seungbum S; Korstanje, Ron R
Publication Date: 2013-09-18

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 24252756
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  • Main text
  • 2050-7771-1-27.pdf
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From diarrhea to obesity in prohormone convertase 1/3 deficiency: age-dependent clinical, pathologic, and enteroendocrine characteristics.

Journal Of Clinical Gastroenterology
Bandsma, Robert H J RH; Sokollik, Christiane C; Chami, Rose R; Cutz, Ernest E; Brubaker, Patricia L PL; Hamilton, Jill K JK; Perlman, Kusiel K; Zlotkin, Stanley S; Sigalet, David L DL; Sherman, Philip M PM; Martin, Martin G MG; Avitzur, Yaron Y
Publication Date: 2013

Variant appearance in text: rs6232
PubMed Link: 24135795
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The regulated secretory pathway and human disease: insights from gene variants and single nucleotide polymorphisms.

Frontiers In Endocrinology
Lin, Wei-Jye WJ; Salton, Stephen R SR
Publication Date: 2013

Variant appearance in text: rs6232
PubMed Link: 23964269
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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.

Nature Genetics
Berndt, Sonja I SI; Gustafsson, Stefan S; Mägi, Reedik R; Ganna, Andrea A; Wheeler, Eleanor E; Feitosa, Mary F MF; Justice, Anne E AE; Monda, Keri L KL; Croteau-Chonka, Damien C DC; Day, Felix R FR; Esko, Tõnu T; Fall, Tove T; Ferreira, Teresa T; Gentilini, Davide D; Jackson, Anne U AU; Luan, Jian'an J; Randall, Joshua C JC; Vedantam, Sailaja S; Willer, Cristen J CJ; Winkler, Thomas W TW; Wood, Andrew R AR; Workalemahu, Tsegaselassie T; Hu, Yi-Juan YJ; Lee, Sang Hong SH; Liang, Liming L; Lin, Dan-Yu DY; Min, Josine L JL; Neale, Benjamin M BM; Thorleifsson, Gudmar G; Yang, Jian J; Albrecht, Eva E; Amin, Najaf N; Bragg-Gresham, Jennifer L JL; Cadby, Gemma G; den Heijer, Martin M; Eklund, Niina N; Fischer, Krista K; Goel, Anuj A; Hottenga, Jouke-Jan JJ; Huffman, Jennifer E JE; Jarick, Ivonne I; Johansson, Åsa Å; Johnson, Toby T; Kanoni, Stavroula S; Kleber, Marcus E ME; König, Inke R IR; Kristiansson, Kati K; Kutalik, Zoltán Z; Lamina, Claudia C; Lecoeur, Cecile C; Li, Guo G; Mangino, Massimo M; McArdle, Wendy L WL; Medina-Gomez, Carolina C; Müller-Nurasyid, Martina M; Ngwa, Julius S JS; Nolte, Ilja M IM; Paternoster, Lavinia L; Pechlivanis, Sonali S; Perola, Markus M; Peters, Marjolein J MJ; Preuss, Michael M; Rose, Lynda M LM; Shi, Jianxin J; Shungin, Dmitry D; Smith, Albert Vernon AV; Strawbridge, Rona J RJ; Surakka, Ida I; Teumer, Alexander A; Trip, Mieke D MD; Tyrer, Jonathan J; Van Vliet-Ostaptchouk, Jana V JV; Vandenput, Liesbeth L; Waite, Lindsay L LL; Zhao, Jing Hua JH; Absher, Devin D; Asselbergs, Folkert W FW; Atalay, Mustafa M; Attwood, Antony P AP; Balmforth, Anthony J AJ; Basart, Hanneke H; Beilby, John J; Bonnycastle, Lori L LL; Brambilla, Paolo P; Bruinenberg, Marcel M; Campbell, Harry H; Chasman, Daniel I DI; Chines, Peter S PS; Collins, Francis S FS; Connell, John M JM; Cookson, William O WO; de Faire, Ulf U; de Vegt, Femmie F; Dei, Mariano M; Dimitriou, Maria M; Edkins, Sarah S; Estrada, Karol K; Evans, David M DM; Farrall, Martin M; Ferrario, Marco M MM; Ferrières, Jean J; Franke, Lude L; Frau, Francesca F; Gejman, Pablo V PV; Grallert, Harald H; Grönberg, Henrik H; Gudnason, Vilmundur V; Hall, Alistair S AS; Hall, Per P; Hartikainen, Anna-Liisa AL; Hayward, Caroline C; Heard-Costa, Nancy L NL; Heath, Andrew C AC; Hebebrand, Johannes J; Homuth, Georg G; Hu, Frank B FB; Hunt, Sarah E SE; Hyppönen, Elina E; Iribarren, Carlos C; Jacobs, Kevin B KB; Jansson, John-Olov JO; Jula, Antti A; Kähönen, Mika M; Kathiresan, Sekar S; Kee, Frank F; Khaw, Kay-Tee KT; Kivimäki, Mika M; Koenig, Wolfgang W; Kraja, Aldi T AT; Kumari, Meena M; Kuulasmaa, Kari K; Kuusisto, Johanna J; Laitinen, Jaana H JH; Lakka, Timo A TA; Langenberg, Claudia C; Launer, Lenore J LJ; Lind, Lars L; Lindström, Jaana J; Liu, Jianjun J; Liuzzi, Antonio A; Lokki, Marja-Liisa ML; Lorentzon, Mattias M; Madden, Pamela A PA; Magnusson, Patrik K PK; Manunta, Paolo P; Marek, Diana D; März, Winfried W; Mateo Leach, Irene I; McKnight, Barbara B; Medland, Sarah E SE; Mihailov, Evelin E; Milani, Lili L; Montgomery, Grant W GW; Mooser, Vincent V; Mühleisen, Thomas W TW; Munroe, Patricia B PB; Musk, Arthur W AW; Narisu, Narisu N; Navis, Gerjan G; Nicholson, George G; Nohr, Ellen A EA; Ong, Ken K KK; Oostra, Ben A BA; Palmer, Colin N A CN; Palotie, Aarno A; Peden, John F JF; Pedersen, Nancy N; Peters, Annette A; Polasek, Ozren O; Pouta, Anneli A; Pramstaller, Peter P PP; Prokopenko, Inga I; Pütter, Carolin C; Radhakrishnan, Aparna A; Raitakari, Olli O; Rendon, Augusto A; Rivadeneira, Fernando F; Rudan, Igor I; Saaristo, Timo E TE; Sambrook, Jennifer G JG; Sanders, Alan R AR; Sanna, Serena S; Saramies, Jouko J; Schipf, Sabine S; Schreiber, Stefan S; Schunkert, Heribert H; Shin, So-Youn SY; Signorini, Stefano S; Sinisalo, Juha J; Skrobek, Boris B; Soranzo, Nicole N; Stančáková, Alena A; Stark, Klaus K; Stephens, Jonathan C JC; Stirrups, Kathleen K; Stolk, Ronald P RP; Stumvoll, Michael M; Swift, Amy J AJ; Theodoraki, Eirini V EV; Thorand, Barbara B; Tregouet, David-Alexandre DA; Tremoli, Elena E; Van der Klauw, Melanie M MM; van Meurs, Joyce B J JB; Vermeulen, Sita H SH; Viikari, Jorma J; Virtamo, Jarmo J; Vitart, Veronique V; Waeber, Gérard G; Wang, Zhaoming Z; Widén, Elisabeth E; Wild, Sarah H SH; Willemsen, Gonneke G; Winkelmann, Bernhard R BR; Witteman, Jacqueline C M JC; Wolffenbuttel, Bruce H R BH; Wong, Andrew A; Wright, Alan F AF; Zillikens, M Carola MC; Amouyel, Philippe P; Boehm, Bernhard O BO; Boerwinkle, Eric E; Boomsma, Dorret I DI; Caulfield, Mark J MJ; Chanock, Stephen J SJ; Cupples, L Adrienne LA; Cusi, Daniele D; Dedoussis, George V GV; Erdmann, Jeanette J; Eriksson, Johan G JG; Franks, Paul W PW; Froguel, Philippe P; Gieger, Christian C; Gyllensten, Ulf U; Hamsten, Anders A; Harris, Tamara B TB; Hengstenberg, Christian C; Hicks, Andrew A AA; Hingorani, Aroon A; Hinney, Anke A; Hofman, Albert A; Hovingh, Kees G KG; Hveem, Kristian K; Illig, Thomas T; Jarvelin, Marjo-Riitta MR; Jöckel, Karl-Heinz KH; Keinanen-Kiukaanniemi, Sirkka M SM; Kiemeney, Lambertus A LA; Kuh, Diana D; Laakso, Markku M; Lehtimäki, Terho T; Levinson, Douglas F DF; Martin, Nicholas G NG; Metspalu, Andres A; Morris, Andrew D AD; Nieminen, Markku S MS; Njølstad, Inger I; Ohlsson, Claes C; Oldehinkel, Albertine J AJ; Ouwehand, Willem H WH; Palmer, Lyle J LJ; Penninx, Brenda B; Power, Chris C; Province, Michael A MA; Psaty, Bruce M BM; Qi, Lu L; Rauramaa, Rainer R; Ridker, Paul M PM; Ripatti, Samuli S; Salomaa, Veikko V; Samani, Nilesh J NJ; Snieder, Harold H; Sørensen, Thorkild I A TI; Spector, Timothy D TD; Stefansson, Kari K; Tönjes, Anke A; Tuomilehto, Jaakko J; Uitterlinden, André G AG; Uusitupa, Matti M; van der Harst, Pim P; Vollenweider, Peter P; Wallaschofski, Henri H; Wareham, Nicholas J NJ; Watkins, Hugh H; Wichmann, H-Erich HE; Wilson, James F JF; Abecasis, Goncalo R GR; Assimes, Themistocles L TL; Barroso, Inês I; Boehnke, Michael M; Borecki, Ingrid B IB; Deloukas, Panos P; Fox, Caroline S CS; Frayling, Timothy T; Groop, Leif C LC; Haritunian, Talin T; Heid, Iris M IM; Hunter, David D; Kaplan, Robert C RC; Karpe, Fredrik F; Moffatt, Miriam F MF; Mohlke, Karen L KL; O'Connell, Jeffrey R JR; Pawitan, Yudi Y; Schadt, Eric E EE; Schlessinger, David D; Steinthorsdottir, Valgerdur V; Strachan, David P DP; Thorsteinsdottir, Unnur U; van Duijn, Cornelia M CM; Visscher, Peter M PM; Di Blasio, Anna Maria AM; Hirschhorn, Joel N JN; Lindgren, Cecilia M CM; Morris, Andrew P AP; Meyre, David D; Scherag, André A; McCarthy, Mark I MI; Speliotes, Elizabeth K EK; North, Kari E KE; Loos, Ruth J F RJ; Ingelsson, Erik E
Publication Date: 2013-05

Variant appearance in text: rs6232
PubMed Link: 23563607
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Contribution of common PCSK1 genetic variants to obesity in 8,359 subjects from multi-ethnic American population.

Plos One
Choquet, Hélène H; Kasberger, Jay J; Hamidovic, Ajna A; Jorgenson, Eric E
Publication Date: 2013

Variant appearance in text: rs6232
PubMed Link: 23451278
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Functional consequences of a novel variant of PCSK1.

Plos One
Pickett, Lindsay A LA; Yourshaw, Michael M; Albornoz, Valeria V; Chen, Zijun Z; Solorzano-Vargas, R Sergio RS; Nelson, Stanley F SF; Martín, Martín G MG; Lindberg, Iris I
Publication Date: 2013

Variant appearance in text: PC1/3: N221D; rs6232
PubMed Link: 23383060
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The genetics of human obesity.

Annals Of The New York Academy Of Sciences
Xia, Qianghua Q; Grant, Struan F A SF
Publication Date: 2013-04

Variant appearance in text: PCSK1: N221D
PubMed Link: 23360386
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Developmental origins of genotype-phenotype correlations in chronic diseases of old age.

Aging And Disease
McCormack, Shana S; Xia, Qianghua Q; Grant, Struan F A SF
Publication Date: 2012-10

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 23185719
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Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases.

Bmc Medical Genetics
Huhn, Stefanie S; Bevier, Melanie M; Rudolph, Anja A; Pardini, Barbara B; Naccarati, Alessio A; Hein, Rebecca R; Hoffmeister, Michael M; Vodickova, Ludmila L; Novotny, Jan J; Brenner, Hermann H; Chang-Claude, Jenny J; Hemminki, Kari K; Vodicka, Pavel P; Försti, Asta A
Publication Date: 2012-10-05

Variant appearance in text: rs6232
PubMed Link: 23036011
Variant Present in the following documents:
  • 1471-2350-13-94-S1.pdf
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PCSK1 rs6232 is associated with childhood and adult class III obesity in the Mexican population.

Plos One
Villalobos-Comparán, Marisela M; Villamil-Ramírez, Hugo H; Villarreal-Molina, Teresa T; Larrieta-Carrasco, Elena E; León-Mimila, Paola P; Romero-Hidalgo, Sandra S; Jacobo-Albavera, Leonor L; Liceaga-Fuentes, Adriana E AE; Campos-Pérez, Francisco J FJ; López-Contreras, Blanca E BE; Tusié-Luna, Teresa T; Del Río-Navarro, Blanca E BE; Aguilar-Salinas, Carlos A CA; Canizales-Quinteros, Samuel S
Publication Date: 2012

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 22737226
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A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.

Nature Genetics
Manning, Alisa K AK; Hivert, Marie-France MF; Scott, Robert A RA; Grimsby, Jonna L JL; Bouatia-Naji, Nabila N; Chen, Han H; Rybin, Denis D; Liu, Ching-Ti CT; Bielak, Lawrence F LF; Prokopenko, Inga I; Amin, Najaf N; Barnes, Daniel D; Cadby, Gemma G; Hottenga, Jouke-Jan JJ; Ingelsson, Erik E; Jackson, Anne U AU; Johnson, Toby T; Kanoni, Stavroula S; Ladenvall, Claes C; Lagou, Vasiliki V; Lahti, Jari J; Lecoeur, Cecile C; Liu, Yongmei Y; Martinez-Larrad, Maria Teresa MT; Montasser, May E ME; Navarro, Pau P; Perry, John R B JR; Rasmussen-Torvik, Laura J LJ; Salo, Perttu P; Sattar, Naveed N; Shungin, Dmitry D; Strawbridge, Rona J RJ; Tanaka, Toshiko T; van Duijn, Cornelia M CM; An, Ping P; de Andrade, Mariza M; Andrews, Jeanette S JS; Aspelund, Thor T; Atalay, Mustafa M; Aulchenko, Yurii Y; Balkau, Beverley B; Bandinelli, Stefania S; Beckmann, Jacques S JS; Beilby, John P JP; Bellis, Claire C; Bergman, Richard N RN; Blangero, John J; Boban, Mladen M; Boehnke, Michael M; Boerwinkle, Eric E; Bonnycastle, Lori L LL; Boomsma, Dorret I DI; Borecki, Ingrid B IB; Böttcher, Yvonne Y; Bouchard, Claude C; Brunner, Eric E; Budimir, Danijela D; Campbell, Harry H; Carlson, Olga O; Chines, Peter S PS; Clarke, Robert R; Collins, Francis S FS; Corbatón-Anchuelo, Arturo A; Couper, David D; de Faire, Ulf U; Dedoussis, George V GV; Deloukas, Panos P; Dimitriou, Maria M; Egan, Josephine M JM; Eiriksdottir, Gudny G; Erdos, Michael R MR; Eriksson, Johan G JG; Eury, Elodie E; Ferrucci, Luigi L; Ford, Ian I; Forouhi, Nita G NG; Fox, Caroline S CS; Franzosi, Maria Grazia MG; Franks, Paul W PW; Frayling, Timothy M TM; Froguel, Philippe P; Galan, Pilar P; de Geus, Eco E; Gigante, Bruna B; Glazer, Nicole L NL; Goel, Anuj A; Groop, Leif L; Gudnason, Vilmundur V; Hallmans, Göran G; Hamsten, Anders A; Hansson, Ola O; Harris, Tamara B TB; Hayward, Caroline C; Heath, Simon S; Hercberg, Serge S; Hicks, Andrew A AA; Hingorani, Aroon A; Hofman, Albert A; Hui, Jennie J; Hung, Joseph J; Jarvelin, Marjo-Riitta MR; Jhun, Min A MA; Johnson, Paul C D PC; Jukema, J Wouter JW; Jula, Antti A; Kao, W H WH; Kaprio, Jaakko J; Kardia, Sharon L R SL; Keinanen-Kiukaanniemi, Sirkka S; Kivimaki, Mika M; Kolcic, Ivana I; Kovacs, Peter P; Kumari, Meena M; Kuusisto, Johanna J; Kyvik, Kirsten Ohm KO; Laakso, Markku M; Lakka, Timo T; Lannfelt, Lars L; Lathrop, G Mark GM; Launer, Lenore J LJ; Leander, Karin K; Li, Guo G; Lind, Lars L; Lindstrom, Jaana J; Lobbens, Stéphane S; Loos, Ruth J F RJ; Luan, Jian'an J; Lyssenko, Valeriya V; Mägi, Reedik R; Magnusson, Patrik K E PK; Marmot, Michael M; Meneton, Pierre P; Mohlke, Karen L KL; Mooser, Vincent V; Morken, Mario A MA; Miljkovic, Iva I; Narisu, Narisu N; O'Connell, Jeff J; Ong, Ken K KK; Oostra, Ben A BA; Palmer, Lyle J LJ; Palotie, Aarno A; Pankow, James S JS; Peden, John F JF; Pedersen, Nancy L NL; Pehlic, Marina M; Peltonen, Leena L; Penninx, Brenda B; Pericic, Marijana M; Perola, Markus M; Perusse, Louis L; Peyser, Patricia A PA; Polasek, Ozren O; Pramstaller, Peter P PP; Province, Michael A MA; Räikkönen, Katri K; Rauramaa, Rainer R; Rehnberg, Emil E; Rice, Ken K; Rotter, Jerome I JI; Rudan, Igor I; Ruokonen, Aimo A; Saaristo, Timo T; Sabater-Lleal, Maria M; Salomaa, Veikko V; Savage, David B DB; Saxena, Richa R; Schwarz, Peter P; Seedorf, Udo U; Sennblad, Bengt B; Serrano-Rios, Manuel M; Shuldiner, Alan R AR; Sijbrands, Eric J G EJ; Siscovick, David S DS; Smit, Johannes H JH; Small, Kerrin S KS; Smith, Nicholas L NL; Smith, Albert Vernon AV; Stančáková, Alena A; Stirrups, Kathleen K; Stumvoll, Michael M; Sun, Yan V YV; Swift, Amy J AJ; Tönjes, Anke A; Tuomilehto, Jaakko J; Trompet, Stella S; Uitterlinden, Andre G AG; Uusitupa, Matti M; Vikström, Max M; Vitart, Veronique V; Vohl, Marie-Claude MC; Voight, Benjamin F BF; Vollenweider, Peter P; Waeber, Gerard G; Waterworth, Dawn M DM; Watkins, Hugh H; Wheeler, Eleanor E; Widen, Elisabeth E; Wild, Sarah H SH; Willems, Sara M SM; Willemsen, Gonneke G; Wilson, James F JF; Witteman, Jacqueline C M JC; Wright, Alan F AF; Yaghootkar, Hanieh H; Zelenika, Diana D; Zemunik, Tatijana T; Zgaga, Lina L; , ; , ; Wareham, Nicholas J NJ; McCarthy, Mark I MI; Barroso, Ines I; Watanabe, Richard M RM; Florez, Jose C JC; Dupuis, Josée J; Meigs, James B JB; Langenberg, Claudia C
Publication Date: 2012-05-13

Variant appearance in text: PCSK1: N221D; rs6232
PubMed Link: 22581228
Variant Present in the following documents:
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