Bioethical issues of preventing hereditary diseases with late onset in the Sakha Republic (Yakutia)

por Kononova, Sardana K., Sidorova, Oksana G., Fedorova, Sardana A., Platonov, Fedor A., Izhevskaya, Vera L., Khusnutdinova, Elza K.
Publicado 2014

Ethylene-Cytokinin Interaction Determines Early Defense Response of Wheat against Stagonospora nodorum Berk.

por Veselova, Svetlana V., Nuzhnaya, Tatyana V., Burkhanova, Guzel F., Rumyantsev, Sergey D., Khusnutdinova, Elza K., Maksimov, Igor V.
Publicado 2021

Decreased Rate of Evolution in Y Chromosome STR Loci of Increased Size of the Repeat Unit

por Järve, Mari, Zhivotovsky, Lev A., Rootsi, Siiri, Help, Hela, Rogaev, Evgeny I., Khusnutdinova, Elza K., Kivisild, Toomas, Sanchez, Juan J.
Publicado 2009

A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia

por Romanov, Georgii P., Pshennikova, Vera G., Lashin, Sergey A., Solovyev, Aisen V., Teryutin, Fedor M., Cherdonova, Aleksandra M., Borisova, Tuyara V., Sazonov, Nikolay N., Khusnutdinova, Elza K., Posukh, Olga L., Fedorova, Sardana A., Barashkov, Nikolay A.
Publicado 2020

Y-chromosomal connection between Hungarians and geographically distant populations of the Ural Mountain region and West Siberia

por Post, Helen, Németh, Endre, Klima, László, Flores, Rodrigo, Fehér, Tibor, Türk, Attila, Székely, Gábor, Sahakyan, Hovhannes, Mondal, Mayukh, Montinaro, Francesco, Karmin, Monika, Saag, Lauri, Yunusbayev, Bayazit, Khusnutdinova, Elza K., Metspalu, Ene, Villems, Richard, Tambets, Kristiina, Rootsi, Siiri
Publicado 2019

A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C>T (p.Arg259*) in the MITF gene in Yakut patient from the Eastern Siberia (Sakha R...

por Barashkov, Nikolay A., Romanov, Georgii P., Borisova, Uigulaana P., Solovyev, Aisen V., Pshennikova, Vera G., Teryutin, Fedor M., Bondar, Alexander A., Morozov, Igor V., Khusnutdinova, Elza K., Posukh, Olga L., Burtseva, Tatiana E., Odland, Jon Øyvind, Fedorova, Sardana A.
Publicado 2019

Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia

por Fedorova, Sardana A, Reidla, Maere, Metspalu, Ene, Metspalu, Mait, Rootsi, Siiri, Tambets, Kristiina, Trofimova, Natalya, Zhadanov, Sergey I, Kashani, Baharak Hooshiar, Olivieri, Anna, Voevoda, Mikhail I, Osipova, Ludmila P, Platonov, Fedor A, Tomsky, Mikhail I, Khusnutdinova, Elza K, Torroni, Antonio, Villems, Richard
Publicado 2013

Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A)

por Pshennikova, Vera G., Barashkov, Nikolay A., Romanov, Georgii P., Teryutin, Fedor M., Solov'ev, Aisen V., Gotovtsev, Nyurgun N., Nikanorova, Alena A., Nakhodkin, Sergey S., Sazonov, Nikolay N., Morozov, Igor V., Bondar, Alexander A., Dzhemileva, Lilya U., Khusnutdinova, Elza K., Posukh, Olga L., Fedorova, Sardana A.
Publicado 2019

Origin and diffusion of human Y chromosome haplogroup J1-M267

por Sahakyan, Hovhannes, Margaryan, Ashot, Saag, Lauri, Karmin, Monika, Flores, Rodrigo, Haber, Marc, Kushniarevich, Alena, Khachatryan, Zaruhi, Bahmanimehr, Ardeshir, Parik, Jüri, Karafet, Tatiana, Yunusbayev, Bayazit, Reisberg, Tuuli, Solnik, Anu, Metspalu, Ene, Hovhannisyan, Anahit, Khusnutdinova, Elza K., Behar, Doron M., Metspalu, Mait, Yepiskoposyan, Levon, Rootsi, Siiri, Villems, Richard
Publicado 2021

Age-Related Hearing Impairment (ARHI) Associated with GJB2 Single Mutation IVS1+1G>A in the Yakut Population Isolate in Eastern Siberia

por Barashkov, Nikolay A., Teryutin, Fedor M., Pshennikova, Vera G., Solovyev, Aisen V., Klarov, Leonid A., Solovyeva, Natalya A., Kozhevnikov, Andrei A., Vasilyeva, Lena M., Fedotova, Elvira E., Pak, Maria V., Lekhanova, Sargylana N., Zakharova, Elena V., Savvinova, Kyunney E., Gotovtsev, Nyurgun N., Rafailo, Adyum M., Luginov, Nikolay V., Alexeev, Anatoliy N., Posukh, Olga L., Dzhemileva, Lilya U., Khusnutdinova, Elza K., Fedorova, Sardana A.
Publicado 2014

Between Lake Baikal and the Baltic Sea: genomic history of the gateway to Europe

por Triska, Petr, Chekanov, Nikolay, Stepanov, Vadim, Khusnutdinova, Elza K., Kumar, Ganesh Prasad Arun, Akhmetova, Vita, Babalyan, Konstantin, Boulygina, Eugenia, Kharkov, Vladimir, Gubina, Marina, Khidiyatova, Irina, Khitrinskaya, Irina, Khrameeva, Ekaterina E., Khusainova, Rita, Konovalova, Natalia, Litvinov, Sergey, Marusin, Andrey, Mazur, Alexandr M., Puzyrev, Valery, Ivanoshchuk, Dinara, Spiridonova, Maria, Teslyuk, Anton, Tsygankova, Svetlana, Triska, Martin, Trofimova, Natalya, Vajda, Edward, Balanovsky, Oleg, Baranova, Ancha, Skryabin, Konstantin, Tatarinova, Tatiana V., Prokhortchouk, Egor
Publicado 2017

Spectrum and Frequency of the GJB2 Gene Pathogenic Variants in a Large Cohort of Patients with Hearing Impairment Living in a Subarctic Region of Russia (the Sakha Republic)

por Barashkov, Nikolay A., Pshennikova, Vera G., Posukh, Olga L., Teryutin, Fedor M., Solovyev, Aisen V., Klarov, Leonid A., Romanov, Georgii P., Gotovtsev, Nyurgun N., Kozhevnikov, Andrey A., Kirillina, Elena V., Sidorova, Oksana G., Vasilyevа, Lena M., Fedotova, Elvira E., Morozov, Igor V., Bondar, Alexander A., Solovyevа, Natalya A., Kononova, Sardana K., Rafailov, Adyum M., Sazonov, Nikolay N., Alekseev, Anatoliy N., Tomsky, Mikhail I., Dzhemileva, Lilya U., Khusnutdinova, Elza K., Fedorova, Sardana A.
Publicado 2016

Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations

por Tambets, Kristiina, Yunusbayev, Bayazit, Hudjashov, Georgi, Ilumäe, Anne-Mai, Rootsi, Siiri, Honkola, Terhi, Vesakoski, Outi, Atkinson, Quentin, Skoglund, Pontus, Kushniarevich, Alena, Litvinov, Sergey, Reidla, Maere, Metspalu, Ene, Saag, Lehti, Rantanen, Timo, Karmin, Monika, Parik, Jüri, Zhadanov, Sergey I., Gubina, Marina, Damba, Larisa D., Bermisheva, Marina, Reisberg, Tuuli, Dibirova, Khadizhat, Evseeva, Irina, Nelis, Mari, Klovins, Janis, Metspalu, Andres, Esko, Tõnu, Balanovsky, Oleg, Balanovska, Elena, Khusnutdinova, Elza K., Osipova, Ludmila P., Voevoda, Mikhail, Villems, Richard, Kivisild, Toomas, Metspalu, Mait
Publicado 2018

Opening up new horizons for psychiatric genetics in the Russian Federation: moving toward a national consortium

por Fedorenko, Olga Yu., Golimbet, Vera E., Ivanova, Svetlana А., Levchenko, Аnastasia, Gainetdinov, Raul R., Semke, Arkady V., Simutkin, German G., Gareeva, Аnna E., Glotov, Аndrey S., Gryaznova, Anna, Iourov, Ivan Y., Krupitsky, Evgeny M., Lebedev, Igor N., Mazo, Galina E., Kaleda, Vasily G., Abramova, Lilia I., Oleichik, Igor V., Nasykhova, Yulia A., Nasyrova, Regina F., Nikolishin, Anton E., Kasyanov, Evgeny D., Rukavishnikov, Grigory V., Timerbulatov, Ilgiz F., Brodyansky, Vadim M., Vorsanova, Svetlana G., Yurov, Yury B., Zhilyaeva, Tatyana V., Sergeeva, Anzhelika V., Blokhina, Elena A., Zvartau, Edwin E., Blagonravova, Anna S., Aftanas, Lyubomir I., Bokhan, Nikolay А., Kekelidze, Zurab I., Klimenko, Tatyana V., Anokhina, Irina P., Khusnutdinova, Elza K., Klyushnik, Tatyana P., Neznanov, Nikolay G., Stepanov, Vadim A., Schulze, Thomas G., Kibitov, Аleksandr О.
Publicado 2019

Origin and spread of human mitochondrial DNA haplogroup U7

por Sahakyan, Hovhannes, Hooshiar Kashani, Baharak, Tamang, Rakesh, Kushniarevich, Alena, Francis, Amirtharaj, Costa, Marta D, Pathak, Ajai Kumar, Khachatryan, Zaruhi, Sharma, Indu, van Oven, Mannis, Parik, Jüri, Hovhannisyan, Hrant, Metspalu, Ene, Pennarun, Erwan, Karmin, Monika, Tamm, Erika, Tambets, Kristiina, Bahmanimehr, Ardeshir, Reisberg, Tuuli, Reidla, Maere, Achilli, Alessandro, Olivieri, Anna, Gandini, Francesca, Perego, Ugo A., Al-Zahery, Nadia, Houshmand, Massoud, Sanati, Mohammad Hossein, Soares, Pedro, Rai, Ekta, Šarac, Jelena, Šarić, Tena, Sharma, Varun, Pereira, Luisa, Fernandes, Veronica, Černý, Viktor, Farjadian, Shirin, Singh, Deepankar Pratap, Azakli, Hülya, Üstek, Duran, Ekomasova (Trofimova), Natalia, Kutuev, Ildus, Litvinov, Sergei, Bermisheva, Marina, Khusnutdinova, Elza K., Rai, Niraj, Singh, Manvendra, Singh, Vijay Kumar, Reddy, Alla G., Tolk, Helle-Viivi, Cvjetan, Svjetlana, Lauc, Lovorka Barac, Rudan, Pavao, Michalodimitrakis, Emmanuel N., Anagnou, Nicholas P., Pappa, Kalliopi I., Golubenko, Maria V., Orekhov, Vladimir, Borinskaya, Svetlana A, Kaldma, Katrin, Schauer, Monica A., Simionescu, Maya, Gusar, Vladislava, Grechanina, Elena, Govindaraj, Periyasamy, Voevoda, Mikhail, Damba, Larissa, Sharma, Swarkar, Singh, Lalji, Semino, Ornella, Behar, Doron M., Yepiskoposyan, Levon, Richards, Martin B., Metspalu, Mait, Kivisild, Toomas, Thangaraj, Kumarasamy, Endicott, Phillip, Chaubey, Gyaneshwer, Torroni, Antonio, Villems, Richard
Publicado 2017

Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

por Figlioli, Gisella, Billaud, Amandine, Wang, Qin, Bolla, Manjeet K., Dennis, Joe, Lush, Michael, Kvist, Anders, Adank, Muriel A., Ahearn, Thomas U., Antonenkova, Natalia N., Auvinen, Päivi, Behrens, Sabine, Bermisheva, Marina, Bogdanova, Natalia V., Bojesen, Stig E., Bonanni, Bernardo, Brüning, Thomas, Camp, Nicola J., Campbell, Archie, Castelao, Jose E., Cessna, Melissa H., Czene, Kamila, Devilee, Peter, Dörk, Thilo, Eriksson, Mikael, Fasching, Peter A., Flyger, Henrik, Gabrielson, Marike, Gago-Dominguez, Manuela, García-Closas, Montserrat, Glendon, Gord, Gómez Garcia, Encarna B., González-Neira, Anna, Grassmann, Felix, Guénel, Pascal, Hahnen, Eric, Hamann, Ute, Hillemanns, Peter, Hooning, Maartje J., Hoppe, Reiner, Howell, Anthony, Humphreys, Keith, Jakubowska, Anna, Khusnutdinova, Elza K., Kristensen, Vessela N., Lindblom, Annika, Loizidou, Maria A., Lubiński, Jan, Mannermaa, Arto, Maurer, Tabea, Mavroudis, Dimitrios, Newman, William G., Obi, Nadia, Panayiotidis, Mihalis I., Radice, Paolo, Rashid, Muhammad U., Rhenius, Valerie, Ruebner, Matthias, Saloustros, Emmanouil, Sawyer, Elinor J., Schmidt, Marjanka K., Schmutzler, Rita K., Shah, Mitul, Southey, Melissa C., Tomlinson, Ian, Truong, Thérèse, van Veen, Elke M., Wendt, Camilla, Yang, Xiaohong R., Michailidou, Kyriaki, Dunning, Alison M., Pharoah, Paul D. P., Easton, Douglas F., Andrulis, Irene L., Evans, D. Gareth, Hollestelle, Antoinette, Chang-Claude, Jenny, Milne, Roger L., Peterlongo, Paolo
Publicado 2023

A recent bottleneck of Y chromosome diversity coincides with a global change in culture

por Karmin, Monika, Saag, Lauri, Vicente, Mário, Sayres, Melissa A. Wilson, Järve, Mari, Talas, Ulvi Gerst, Rootsi, Siiri, Ilumäe, Anne-Mai, Mägi, Reedik, Mitt, Mario, Pagani, Luca, Puurand, Tarmo, Faltyskova, Zuzana, Clemente, Florian, Cardona, Alexia, Metspalu, Ene, Sahakyan, Hovhannes, Yunusbayev, Bayazit, Hudjashov, Georgi, DeGiorgio, Michael, Loogväli, Eva-Liis, Eichstaedt, Christina, Eelmets, Mikk, Chaubey, Gyaneshwer, Tambets, Kristiina, Litvinov, Sergei, Mormina, Maru, Xue, Yali, Ayub, Qasim, Zoraqi, Grigor, Korneliussen, Thorfinn Sand, Akhatova, Farida, Lachance, Joseph, Tishkoff, Sarah, Momynaliev, Kuvat, Ricaut, François-Xavier, Kusuma, Pradiptajati, Razafindrazaka, Harilanto, Pierron, Denis, Cox, Murray P., Sultana, Gazi Nurun Nahar, Willerslev, Rane, Muller, Craig, Westaway, Michael, Lambert, David, Skaro, Vedrana, Kovačevic´, Lejla, Turdikulova, Shahlo, Dalimova, Dilbar, Khusainova, Rita, Trofimova, Natalya, Akhmetova, Vita, Khidiyatova, Irina, Lichman, Daria V., Isakova, Jainagul, Pocheshkhova, Elvira, Sabitov, Zhaxylyk, Barashkov, Nikolay A., Nymadawa, Pagbajabyn, Mihailov, Evelin, Seng, Joseph Wee Tien, Evseeva, Irina, Migliano, Andrea Bamberg, Abdullah, Syafiq, Andriadze, George, Primorac, Dragan, Atramentova, Lubov, Utevska, Olga, Yepiskoposyan, Levon, Marjanovic´, Damir, Kushniarevich, Alena, Behar, Doron M., Gilissen, Christian, Vissers, Lisenka, Veltman, Joris A., Balanovska, Elena, Derenko, Miroslava, Malyarchuk, Boris, Metspalu, Andres, Fedorova, Sardana, Eriksson, Anders, Manica, Andrea, Mendez, Fernando L., Karafet, Tatiana M., Veeramah, Krishna R., Bradman, Neil, Hammer, Michael F., Osipova, Ludmila P., Balanovsky, Oleg, Khusnutdinova, Elza K., Johnsen, Knut, Remm, Maido, Thomas, Mark G., Tyler-Smith, Chris, Underhill, Peter A., Willerslev, Eske, Nielsen, Rasmus, Metspalu, Mait, Villems, Richard, Kivisild, Toomas
Publicado 2015

Genomic analyses inform on migration events during the peopling of Eurasia

por Pagani, Luca, Lawson, Daniel John, Jagoda, Evelyn, Mörseburg, Alexander, Eriksson, Anders, Mitt, Mario, Clemente, Florian, Hudjashov, Georgi, DeGiorgio, Michael, Saag, Lauri, Wall, Jeffrey D., Cardona, Alexia, Mägi, Reedik, Wilson Sayres, Melissa A., Kaewert, Sarah, Inchley, Charlotte, Scheib, Christiana L., Järve, Mari, Karmin, Monika, Jacobs, Guy S., Antao, Tiago, Iliescu, Florin Mircea, Kushniarevich, Alena, Ayub, Qasim, Tyler-Smith, Chris, Xue, Yali, Yunusbayev, Bayazit, Tambets, Kristiina, Mallick, Chandana Basu, Saag, Lehti, Pocheshkhova, Elvira, Andriadze, George, Muller, Craig, Westaway, Michael C., Lambert, David M., Zoraqi, Grigor, Turdikulova, Shahlo, Dalimova, Dilbar, Sabitov, Zhaxylyk, Sultana, Gazi Nurun Nahar, Lachance, Joseph, Tishkoff, Sarah, Momynaliev, Kuvat, Isakova, Jainagul, Damba, Larisa D., Gubina, Marina, Nymadawa, Pagbajabyn, Evseeva, Irina, Atramentova, Lubov, Utevska, Olga, Ricaut, François-Xavier, Brucato, Nicolas, Sudoyo, Herawati, Letellier, Thierry, Cox, Murray P., Barashkov, Nikolay A., Skaro, Vedrana, Mulahasanovic, Lejla, Primorac, Dragan, Sahakyan, Hovhannes, Mormina, Maru, Eichstaedt, Christina A., Lichman, Daria V., Abdullah, Syafiq, Chaubey, Gyaneshwer, Wee, Joseph T. S., Mihailov, Evelin, Karunas, Alexandra, Litvinov, Sergei, Khusainova, Rita, Ekomasova, Natalya, Akhmetova, Vita, Khidiyatova, Irina, Marjanović, Damir, Yepiskoposyan, Levon, Behar, Doron M., Balanovska, Elena, Metspalu, Andres, Derenko, Miroslava, Malyarchuk, Boris, Voevoda, Mikhail, Fedorova, Sardana A., Osipova, Ludmila P., Lahr, Marta Mirazón, Gerbault, Pascale, Leavesley, Matthew, Migliano, Andrea Bamberg, Petraglia, Michael, Balanovsky, Oleg, Khusnutdinova, Elza K., Metspalu, Ene, Thomas, Mark G., Manica, Andrea, Nielsen, Rasmus, Villems, Richard, Willerslev, Eske, Kivisild, Toomas, Metspalu, Mait
Publicado 2016

Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes

por Mavaddat, Nasim, Dorling, Leila, Carvalho, Sara, Allen, Jamie, González-Neira, Anna, Keeman, Renske, Bolla, Manjeet K., Dennis, Joe, Wang, Qin, Ahearn, Thomas U., Andrulis, Irene L., Beckmann, Matthias W., Behrens, Sabine, Benitez, Javier, Bermisheva, Marina, Blomqvist, Carl, Bogdanova, Natalia V., Bojesen, Stig E., Briceno, Ignacio, Brüning, Thomas, Camp, Nicola J., Campbell, Archie, Castelao, Jose E., Chang-Claude, Jenny, Chanock, Stephen J., Chenevix-Trench, Georgia, Christiansen, Hans, Czene, Kamila, Dörk, Thilo, Eriksson, Mikael, Evans, D. Gareth, Fasching, Peter A., Figueroa, Jonine D., Flyger, Henrik, Gabrielson, Marike, Gago-Dominguez, Manuela, Geisler, Jürgen, Giles, Graham G., Guénel, Pascal, Hadjisavvas, Andreas, Hahnen, Eric, Hall, Per, Hamann, Ute, Hartikainen, Jaana M., Hartman, Mikael, Hoppe, Reiner, Howell, Anthony, Jakubowska, Anna, Jung, Audrey, Khusnutdinova, Elza K., Kristensen, Vessela N., Li, Jingmei, Lim, Swee Ho, Lindblom, Annika, Loizidou, Maria A., Lophatananon, Artitaya, Lubiński, Jan, Madsen, Michael J., Mannermaa, Arto, Manoochehri, Mehdi, Margolin, Sara, Mavroudis, Dimitrios, Milne, Roger L., Mohd Taib, Nur Aishah, Morra, Anna, Muir, Kenneth, Obi, Nadia, Osorio, Ana, Park-Simon, Tjoung-Won, Peterlongo, Paolo, Radice, Paolo, Saloustros, Emmanouil, Sawyer, Elinor J., Schmutzler, Rita K., Shah, Mitul, Sim, Xueling, Southey, Melissa C., Thorne, Heather, Tomlinson, Ian, Torres, Diana, Truong, Thérèse, Yip, Cheng Har, Spurdle, Amanda B., Vreeswijk, Maaike P.G., Dunning, Alison M., García-Closas, Montserrat, Pharoah, Paul D.P., Kvist, Anders, Muranen, Taru A., Nevanlinna, Heli, Teo, Soo Hwang, Devilee, Peter, Schmidt, Marjanka K., Easton, Douglas F.
Publicado 2022

Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci

por DeVries, Amber A, Dennis, Joe, Tyrer, Jonathan P, Peng, Pei-Chen, Coetzee, Simon G, Reyes, Alberto L, Plummer, Jasmine T, Davis, Brian D, Chen, Stephanie S, Dezem, Felipe Segato, Aben, Katja K H, Anton-Culver, Hoda, Antonenkova, Natalia N, Beckmann, Matthias W, Beeghly-Fadiel, Alicia, Berchuck, Andrew, Bogdanova, Natalia V, Bogdanova-Markov, Nadja, Brenton, James D, Butzow, Ralf, Campbell, Ian, Chang-Claude, Jenny, Chenevix-Trench, Georgia, Cook, Linda S, DeFazio, Anna, Doherty, Jennifer A, Dörk, Thilo, Eccles, Diana M, Eliassen, A Heather, Fasching, Peter A, Fortner, Renée T, Giles, Graham G, Goode, Ellen L, Goodman, Marc T, Gronwald, Jacek, Håkansson, Niclas, Hildebrandt, Michelle A T, Huff, Chad, Huntsman, David G, Jensen, Allan, Kar, Siddhartha, Karlan, Beth Y, Khusnutdinova, Elza K, Kiemeney, Lambertus A, Kjaer, Susanne K, Kupryjanczyk, Jolanta, Labrie, Marilyne, Lambrechts, Diether, Le, Nhu D, Lubiński, Jan, May, Taymaa, Menon, Usha, Milne, Roger L, Modugno, Francesmary, Monteiro, Alvaro N, Moysich, Kirsten B, Odunsi, Kunle, Olsson, Håkan, Pearce, Celeste L, Pejovic, Tanja, Ramus, Susan J, Riboli, Elio, Riggan, Marjorie J, Romieu, Isabelle, Sandler, Dale P, Schildkraut, Joellen M, Setiawan, V Wendy, Sieh, Weiva, Song, Honglin, Sutphen, Rebecca, Terry, Kathryn L, Thompson, Pamela J, Titus, Linda, Tworoger, Shelley S, Van Nieuwenhuysen, Els, Edwards, Digna Velez, Webb, Penelope M, Wentzensen, Nicolas, Whittemore, Alice S, Wolk, Alicja, Wu, Anna H, Ziogas, Argyrios, Freedman, Matthew L, Lawrenson, Kate, Pharoah, Paul D P, Easton, Douglas F, Gayther, Simon A, Jones, Michelle R
Publicado 2022