Genetic variation in CCDC93 is associated with elevated central systolic blood pressure, impaired arterial relaxation, and mitochondrial dysfunction.

Authors: Kumar, Nitin^1,2 (AUTHOR), Yang, Min-Lee^1,2,3 (AUTHOR), Sun, Pengfei^4,5 (AUTHOR), Hunker, Kristina L.^1,2 (AUTHOR), Li, Jianping⁴ (AUTHOR), Jia, Jia⁴ (AUTHOR), Fan, Fangfang⁴ (AUTHOR), Wang, Jinghua^6,7 (AUTHOR), Ning, Xianjia^6,7 (AUTHOR), Gao, Wei⁸ (AUTHOR), Xu, Ming⁸ (AUTHOR), Zhang, Jifeng¹ (AUTHOR), Chang, Lin¹ (AUTHOR), Chen, Yuqing E.¹ (AUTHOR), Huo, Yong⁴ (AUTHOR), Zhang, Yan^4,9,10 (AUTHOR) drzhy1108@163.com, Ganesh, Santhi K.^1,2 (AUTHOR) drzhy1108@163.com

Source: PLoS Genetics. 9/9/2024, Vol. 20 Issue 9, p1-28. 28p.

Subject Terms: *FREE fatty acids, *CHINESE people, *THORACIC aorta, *GENETIC variation, *GENETIC regulation, *BLOOD pressure, *SYSTOLIC blood pressure

Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility

Authors: Murad, Andrea M., Hill, Hannah L., Wang, Yu, Ghannam, Michael, Yang, Min‐Lee, Pugh, Norma L., Asch, Federico M., Hornsby, Whitney, Driscoll, Anisa, McNamara, Jennifer, Willer, Cristen J., Regalado, Ellen S., Milewicz, Dianna M., Eagle, Kim A., Ganesh, Santhi K.

Source: American journal of medical genetics.Part A. 188(5):1448-1456

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100146658770.0x000001&indx=1&recIds=ETOCvdc_100146658770.0x000001

An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population

Authors: Sun, Pengfei, Zhou, Wei, Fu, Yi, Cheung, Chloe Y Y, Dong, Yujun, Yang, Min-Lee, Zhang, He, Jia, Jia, Huo, Yong, Willer, Cristen J, Chen, Y Eugene, Tang, Clara S, Tse, Hung-Fat, Lam, Karen S L, Gao, Wei, Xu, Ming, Yu, Haiyi, Sham, Pak Chung, Zhang, Yan, Ganesh, Santhi K

Source: Human molecular genetics. 30(9):836-842

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100132704058.0x000001&indx=1&recIds=ETOCvdc_100132704058.0x000001

Epidemiologic and Genetic Associations of Erythropoietin With Blood Pressure, Hypertension, and Coronary Artery Disease

Authors: Sun, Pengfei, Kumar, Nitin, Tin, Adrienne, Zhao, Jing, Brown, Michael R., Lin, Zesen, Yang, Min-Lee, Zheng, Qiwen, Jia, Jia, Bielak, Lawrence F., Yu, Bing, Boerwinkle, Eric, Hunker, Kristina L., Coresh, Josef, Chen, Y. Eugene, Huo, Yong, Kardia, Sharon L.R., Khoriaty, Rami, Zhou, Xiang, Morrison, Alanna C., Zhang, Yan, Ganesh, Santhi K.

Source: Hypertension. 78(5):1555-1566

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100176825166.0x000001&indx=1&recIds=ETOCvdc_100176825166.0x000001

Molecular genetic evaluation of pediatric renovascular hypertension due to renal artery stenosis and abdominal aortic coarctation in neurofibromatosis type 1

Authors: Coleman, Dawn M, Wang, Yu, Yang, Min-Lee, Hunker, Kristina L, Birt, Isabelle, Bergin, Ingrid L, Li, Jun Z, Stanley, James C, Ganesh, Santhi K

Source: Human molecular genetics. 31(3):334-346

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100141070732.0x000001&indx=1&recIds=ETOCvdc_100141070732.0x000001

A Novel Recurrent COL5A1 Genetic Variant Is Associated With a Dysplasia-Associated Arterial Disease Exhibiting Dissections and Fibromuscular Dysplasia

Authors: Richer, Julie, Hill, Hannah L., Wang, Yu, Yang, Min-Lee, Hunker, Kristina L., Lane, Jamie, Blackburn, Susan, Coleman, Dawn M., Eliason, Jonathan, Sillon, Guillaume, D'Agostino, Maria-Daniela, Jetty, Prasad, Mongeon, François-Pierre, Laberge, Anne-Marie, Ryan, Stephen E., Fendrikova-Mahlay, Natalia, Coutinho, Thais, Mathis, Michael R., Zawistowski, Matthew, Hazen, Stanley L., Katz, Alexander E., Gornik, Heather L., Brummett, Chad M., Abecasis, Goncalo, Bergin, Ingrid L., Stanley, James C., Li, Jun Z., Ganesh, Santhi K.

Source: Arteriosclerosis, thrombosis, and vascular biology. 40(11):2686-2699

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100180890498.0x000001&indx=1&recIds=ETOCvdc_100180890498.0x000001

Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia

Authors: Georges, Adrien, Albuisson, Juliette, Berrandou, Takiy, Dupré, Délia, Lorthioir, Aurélien, D'Escamard, Valentina, Di Narzo, Antonio F, Kadian-Dodov, Daniella, Olin, Jeffrey W, Warchol-Celinska, Ewa, Prejbisz, Aleksander, Januszewicz, Andrzej, Bruneval, Patrick, Baranowska, Anna A, Webb, Tom R, Hamby, Stephen E, Samani, Nilesh J, Adlam, David, Fendrikova-Mahlay, Natalia, Hazen, Stanley, Wang, Yu, Yang, Min-Lee, Hunker, Kristina, Combaret, Nicolas, Motreff, Pascal, Chédid, Antoine, Fiquet, Béatrice, Plouin, Pierre-François, Mousseaux, Elie, Azarine, Arshid, Amar, Laurence, Azizi, Michel, Gornik, Heather L, Ganesh, Santhi K, Kovacic, Jason C, Jeunemaitre, Xavier, Bouatia-Naji, Nabila

Source: Cardiovascular research. 117(4):1154-1165

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100130287126.0x000001&indx=1&recIds=ETOCvdc_100130287126.0x000001

Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis

Authors: van Rooij, Frank J.A., Qayyum, Rehan, Smith, Albert V., Zhou, Yi, Trompet, Stella, Tanaka, Toshiko, Keller, Margaux F., Chang, Li-Ching, Schmidt, Helena, Yang, Min-Lee, Chen, Ming-Huei, Hayes, James, Johnson, Andrew D., Yanek, Lisa R., Mueller, Christian, Lange, Leslie, Floyd, James S., Ghanbari, Mohsen, Zonderman, Alan B., Jukema, J. Wouter, Hofman, Albert, van Duijn, Cornelia M., Desch, Karl C., Saba, Yasaman, Ozel, Ayse B., Snively, Beverly M., Wu, Jer-Yuarn, Schmidt, Reinhold, Fornage, Myriam, Klein, Robert J., Fox, Caroline S., Matsuda, Koichi, Kamatani, Naoyuki, Wild, Philipp S., Stott, David J., Ford, Ian, Slagboom, P. Eline, Yang, Jaden, Chu, Audrey Y., Lambert, Amy J., Uitterlinden, André G., Franco, Oscar H., Hofer, Edith, Ginsburg, David, Hu, Bella, Keating, Brendan, Schick, Ursula M., Brody, Jennifer A., Li, Jun Z., Chen, Zhao, Zeller, Tanja, Guralnik, Jack M., Chasman, Daniel I., Peters, Luanne L., Kubo, Michiaki, Becker, Diane M., Li, Jin, Eiriksdottir, Gudny, Rotter, Jerome I., Levy, Daniel, Grossmann, Vera, Patel, Kushang V., Chen, Chien-Hsiun, Ridker, Paul M., Tang, Hua, Launer, Lenore J., Rice, Kenneth M., Li-Gao, Ruifang, Ferrucci, Luigi, Evans, Michelle K., Choudhuri, Avik, Trompouki, Eirini, Abraham, Brian J., Yang, Song, Takahashi, Atsushi, Kamatani, Yoichiro, Kooperberg, Charles, Harris, Tamara B., Jee, Sun Ha, Coresh, Josef, Tsai, Fuu-Jen, Longo, Dan L., Chen, Yuan-Tsong, Felix, Janine F., Yang, Qiong, Psaty, Bruce M., Boerwinkle, Eric, Becker, Lewis C., Mook-Kanamori, Dennis O., Wilson, James G., Gudnason, Vilmundur, O'Donnell, Christopher J., Dehghan, Abbas, Cupples, L. Adrienne, Nalls, Michael A., Morris, Andrew P., Okada, Yukinori, Reiner, Alexander P., Zon, Leonard I., Ganesh, Santhi K.

Source: In The American Journal of Human Genetics 5 January 2017 100(1):51-63

Loss-of-Function Mutations in YY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like Vascular Disease

Authors: Guo, Dong-chuan, Duan, Xue-Yan, Regalado, Ellen S., Mellor-Crummey, Lauren, Kwartler, Callie S., Kim, Dong, Lieberman, Kenneth, de Vries, Bert B.A., Pfundt, Rolph, Schinzel, Albert, Kotzot, Dieter, Shen, Xuetong, Yang, Min-Lee, Bamshad, Michael J., Nickerson, Deborah A., Gornik, Heather L., Ganesh, Santhi K., Braverman, Alan C., Grange, Dorothy K., Milewicz, Dianna M.

Source: In The American Journal of Human Genetics 5 January 2017 100(1):21-30

Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations

Authors: Newton-Cheh, Christopher, Johnson, Toby, Gateva, Vesela, Tobin, Martin D., Bochud, Murielle, Coin, Lachlan, Najjar, Samer S., Zhao, Jing Hua, Heath, Simon C., Eyheramendy, Susana, Papadakis, Konstantinos, Voight, Benjamin F., Scott, Laura J., Zhang, Feng, Farrall, Martin, Tanaka, Toshiko, Wallace, Chris, Chambers, John C., Khaw, Kay-Tee, Nilsson, Peter, van der Harst, Pim, Polidoro, Silvia, Grobbee, Diederick E., Onland-Moret, N. Charlotte, Bots, Michiel L., Wain, Louise V., Elliott, Katherine S., Teumer, Alexander, Luan, Jian’an, Lucas, Gavin, Kuusisto, Johanna, Burton, Paul R., Hadley, David, McArdle, Wendy L., Brown, Morris, Dominiczak, Anna, Newhouse, Stephen J., Samani, Nilesh J., Webster, John, Zeggini, Eleftheria, Beckmann, Jacques S., Bergmann, Sven, Lim, Noha, Song, Kijoung, Vollenweider, Peter, Waeber, Gerard, Waterworth, Dawn M., Yuan, Xin, Groop, Leif, Orho-Melander, Marju, Allione, Alessandra, Di Gregorio, Alessandra, Guarrera, Simonetta, Panico, Salvatore, Ricceri, Fulvio, Romanazzi, Valeria, Sacerdote, Carlotta, Vineis, Paolo, Barroso, Inês, Sandhu, Manjinder S., Luben, Robert N., Crawford, Gabriel J., Jousilahti, Pekka, Perola, Markus, Boehnke, Michael, Bonnycastle, Lori L., Collins, Francis S., Jackson, Anne U., Mohlke, Karen L., Stringham, Heather M., Valle, Timo T., Willer, Cristen J., Bergman, Richard N., Morken, Mario A., Döring, Angela, Gieger, Christian, Illig, Thomas, Meitinger, Thomas, Org, Elin, Pfeufer, Arne, Wichmann, H. Erich, Kathiresan, Sekar, Marrugat, Jaume, O’Donnell, Christopher J., Schwartz, Stephen M., Siscovick, David S., Subirana, Isaac, Freimer, Nelson B., Hartikainen, Anna-Liisa, McCarthy, Mark I., O’Reilly, Paul F., Peltonen, Leena, Pouta, Anneli, de Jong, Paul E., Snieder, Harold, van Gilst, Wiek H., Clarke, Robert, Goel, Anuj, Hamsten, Anders, Peden, John F., Seedorf, Udo, Syvänen, Ann-Christine, Tognoni, Giovanni, Lakatta, Edward G., Sanna, Serena, Scheet, Paul, Schlessinger, David, Scuteri, Angelo, Dörr, Marcus, Ernst, Florian, Felix, Stephan B., Homuth, Georg, Lorbeer, Roberto, Reffelmann, Thorsten, Rettig, Rainer, Völker, Uwe, Galan, Pilar, Gut, Ivo G., Hercberg, Serge, Lathrop, G. Mark, Zeleneka, Diana, Deloukas, Panos, Soranzo, Nicole, Williams, Frances M., Zhai, Guangju, Salomaa, Veikko, Laakso, Markku, Elosua, Roberto, Forouhi, Nita G., Völzke, Henry, Uiterwaal, Cuno S., van der Schouw, Yvonne T, Numans, Mattijs E., Matullo, Giuseppe, Navis, Gerjan, Berglund, Göran, Bingham, Sheila A., Kooner, Jaspal S., Paterson, Andrew D., Connell, John M., Bandinelli, Stefania, Ferrucci, Luigi, Watkins, Hugh, Spector, Tim D., Tuomilehto, Jaakko, Altshuler, David, Strachan, David P., Laan, Maris, Meneton, Pierre, Wareham, Nicholas J., Uda, Manuela, Jarvelin, Marjo-Riitta, Mooser, Vincent, Melander, Olle, Loos, Ruth J.F., Elliott, Paul, Abecasis, Gonçalo R., Caulfield, Mark, Munroe, Patricia B., Ganesh, Santhi K., Chasman, Daniel I., Larson, Martin G., Guo, Xiuqing, Verwoert, Germain, Bis, Joshua C., Gu, Xiangjun, Smith, Albert V., Yang, Min-Lee, Zhang, Yan, Ehret, Georg, Rose, Lynda M., Hwang, Shih-Jen, Papanicolau, George J., Sijbrands, Eric J., Rice, Kenneth, Eiriksdottir, Gudny, Pihur, Vasyl, Ridker, Paul M., Vasan, Ramachandran S., Raffel, Leslie J., Amin, Najaf, Rotter, Jerome I., Liu, Kiang, Launer, Lenore J., Xu, Ming, Morrison, Alanna C., Johnson, Andrew D., Vaidya, Dhananjay, Dehghan, Abbas, Li, Guo, Bouchard, Claude, Harris, Tamara B., Zhang, He, Boerwinkle, Eric, Gao, Wei, Uitterlinden, Andre G., Rivadeneira, Fernando, Hofman, Albert, Franco, Oscar H., Huo, Yong, Witteman, Jacqueline C.M., Gudnason, Vilmundur, Palmas, Walter, van Duijn, Cornelia, Fornage, Myriam, Levy, Daniel, Psaty, Bruce M., Chakravarti, Aravinda

Source: In The American Journal of Human Genetics 3 July 2014 95(1):49-65

Sex-specific genetic architecture of blood pressure

Authors: Yang, Min-Lee, Xu, Chang, Gupte, Trisha, Hoffmann, Thomas J., Iribarren, Carlos, Zhou, Xiang, Ganesh, Santhi K.

Source: Nature Medicine; March 2024, Vol. 30 Issue: 3 p818-828, 11p

Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction

Authors: Saw, Jacqueline, Yang, Min-Lee, Trinder, Mark, Tcheandjieu, Catherine, Xu, Chang, Starovoytov, Andrew, Birt, Isabelle, Mathis, Michael R., Hunker, Kristina L., Schmidt, Ellen M., Jackson, Linda, Fendrikova-Mahlay, Natalia, Zawistowski, Matthew, Brummett, Chad M., Zoellner, Sebastian, Katz, Alexander, Coleman, Dawn M., Swan, Kirby, O'Donnell, Christopher J., Zhou, Xiang, Li, Jun Z., Gornik, Heather L., Assimes, Themistocles L., Stanley, James C., Brunham, Liam R., Ganesh, Santhi K.

Source: Nature communications. 11(1)

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100174555396.0x000001&indx=1&recIds=ETOCvdc_100174555396.0x000001

Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture

Authors: Katz, Alexander E., Yang, Min-Lee, Levin, Michael G., Tcheandjieu, Catherine, Mathis, Michael, Hunker, Kristina, Blackburn, Susan, Eliason, Jonathan L., Coleman, Dawn M., Fendrikova-Mahlay, Natalia, Gornik, Heather L., Karmakar, Monita, Hill, Hannah, Xu, Chang, Zawistowski, Matthew, Brummett, Chad M., Zoellner, Sebastian, Zhou, Xiang, O'Donnell, Christopher J., Douglas, Julie A., Assimes, Themistocles L., Tsao, Phillip S., Li, Jun Z., Damrauer, Scott M., Stanley, James C., Ganesh, Santhi K.

Source: Circulation.Genomic and precision medicine. 15(6):e003496-e003496

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100177064521.0x000001&indx=1&recIds=ETOCvdc_100177064521.0x000001

Genome-wide Association Study Reveals Multiple Nasopharyngeal Carcinoma-Associated Loci within the HLA Region at Chromosome 6p21.3

Authors: Tse, Ka-Po, Su, Wen-Hui, Chang, Kai-Ping, Tsang, Ngan-Ming, Yu, Chia-Jung, Tang, Petrus, See, Lee-Chu, Hsueh, Chuen, Yang, Min-Lee, Hao, Sheng-Po, Li, Hong-Yi, Wang, Ming-Hsi, Liao, Li-Ping, Chen, Lih-Chyang, Lin, Sheue-Rong, Jorgensen, Timothy J., Chang, Yu-Sun, Shugart, Yin Yao

Source: In The American Journal of Human Genetics 14 August 2009 85(2):194-203

Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation

Authors: Adlam, David, Berrandou, Takiy-Eddine, Georges, Adrien, Nelson, Christopher P., Giannoulatou, Eleni, Henry, Joséphine, Ma, Lijiang, Blencowe, Montgomery, Turley, Tamiel N., Yang, Min-Lee, Chopade, Sandesh, Finan, Chris, Braund, Peter S., Sadeg-Sayoud, Ines, Iismaa, Siiri E., Kosel, Matthew L., Zhou, Xiang, Hamby, Stephen E., Cheng, Jenny, Liu, Lu, Tarr, Ingrid, Muller, David W. M., d’Escamard, Valentina, King, Annette, Brunham, Liam R., Baranowska-Clarke, Ania A., Debette, Stéphanie, Amouyel, Philippe, Olin, Jeffrey W., Patil, Snehal, Hesselson, Stephanie E., Junday, Keerat, Kanoni, Stavroula, Aragam, Krishna G., Butterworth, Adam S., Tweet, Marysia S., Gulati, Rajiv, Combaret, Nicolas, Kadian-Dodov, Daniella, Kalman, Jonathan M., Fatkin, Diane, Hingorani, Aroon D., Saw, Jacqueline, Webb, Tom R., Hayes, Sharonne N., Yang, Xia, Ganesh, Santhi K., Olson, Timothy M., Kovacic, Jason C., Graham, Robert M., Samani, Nilesh J., Bouatia-Naji, Nabila

Source: Nature Genetics; June 2023, Vol. 55 Issue: 6 p964-972, 9p

Defining B Cell Epitopes of Ovalbumin for the C57BL/6 Mice Immunized with Recombinant Mycobacterium smegmatis

Authors: Hyo Joon Kim, Yang Min Lee, Joon Sung Hwang, Hoshik Won, Bok Hwan Kim

Source: JOURNAL OF BIOCHEMISTRY AND MOLECULAR BIOLOGY. 32(5):461-467

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN068137019&indx=1&recIds=ETOCRN068137019

GENETIC ASSOCIATION STUDIES OF FIBROMUSCULAR DYSPLASIA IDENTIFY NEW RISK LOCI AND SHARED GENETIC BASIS WITH MORE COMMON VASCULAR DISEASES

Authors: Georges, Adrien, Yang, Min-Lee, Berrandou, Takiy-Eddine, Bakker, Mark, Dikilitas, Ozan, Ma, Lijiang, Satterfield, Benjamin A., Sengupta, Sebanti, Hunker, Kristina L., Amar, Laurence, Lorthioir, Aurélien, Prejbisz, Aleksander, Pappaccogli, Marco, Ruigrok, Ynte, Olin, Jeffrey W., Gornik, Heather L., Rietzschel, Ernst R., Celinska, Ewa Warchol, Januszewicz, Andrzej, Kullo, Iftikhar J., Azizi, Michel, Jeunemaitre, Xavier, Persu, Alexandre, Kovacic, Jason C., Ganesh, Santhi K., Bouatia-Naji, Nabila

Source: Journal of hypertension. 39(1):e267-e267

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100185186843.0x000001&indx=1&recIds=ETOCvdc_100185186843.0x000001

Molecular genetic evaluation of pediatric renovascular hypertension due to renal artery stenosis and abdominal aortic coarctation in neurofibromatosis type 1.

Authors: Coleman, Dawn M, Wang, Yu, Yang, Min-Lee, Hunker, Kristina L, Birt, Isabelle, Bergin, Ingrid L, Li, Jun Z, Stanley, James C, Ganesh, Santhi K

Source: Human Molecular Genetics; Feb2022, Vol. 31 Issue 3, p334-346, 13p

Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.

Authors: Georges, Adrien, Yang, Min-Lee, Berrandou, Takiy-Eddine, Bakker, Mark K., Dikilitas, Ozan, Kiando, Soto Romuald, Ma, Lijiang, Satterfield, Benjamin A., Sengupta, Sebanti, Yu, Mengyao, Deleuze, Jean-François, Dupré, Delia, Hunker, Kristina L., Kyryachenko, Sergiy, Liu, Lu, Sayoud-Sadeg, Ines, Amar, Laurence, Brummett, Chad M., Coleman, Dawn M., d'Escamard, Valentina

Source: Nature Communications; 10/15/2021, Vol. 12 Issue 1, p1-16, 16p

Subject Terms: CARDIOVASCULAR diseases, CORONARY artery disease, DYSPLASIA, GENOME-wide association studies, CYTOSKELETON, NUTRITIONAL genomics, LOCUS (Genetics), ANATOMICAL variation

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