S
Sandra Penske
Researcher at Max Planck Society
Publications - 6
Citations - 307
Sandra Penske is an academic researcher from Max Planck Society. The author has contributed to research in topics: Bronze Age & European union. The author has an hindex of 3, co-authored 5 publications receiving 182 citations.
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Journal ArticleDOI
Paleolithic to Bronze Age Siberians Reveal Connections with First Americans and across Eurasia
He Yu,Maria A. Spyrou,Marina K. Karapetian,Svetlana Shnaider,Rita Radzevičiūtė,Kathrin Nägele,Gunnar U. Neumann,Sandra Penske,Jana Zech,Mary Lucas,Petrus LeRoux,Patrick Roberts,G.D. Pavlenok,Alexandra P. Buzhilova,Cosimo Posth,Cosimo Posth,Choongwon Jeong,Choongwon Jeong,Johannes Krause +18 more
TL;DR: This study demonstrates the most deeply divergent connection between Upper Paleolithic Siberians and the First Americans and reveals human and pathogen mobility across Eurasia during the Bronze Age.
Journal ArticleDOI
Genomic history of Neolithic to Bronze Age Anatolia, Northern Levant, and Southern Caucasus
Eirini Skourtanioti,Yılmaz Selim Erdal,Marcella Frangipane,Francesca Balossi Restelli,K. Aslıhan Yener,Frances Pinnock,Paolo Matthiae,Rana Özbal,Ulf-Dietrich Schoop,Farhad Guliyev,Tufan I. Akhundov,Bertille Lyonnet,Emily Hammer,Selin Nugent,Marta Burri,Gunnar U. Neumann,Sandra Penske,Tara Ingman,Murat Akar,Rula Shafiq,Giulio Palumbi,Stefanie Eisenmann,Marta D’Andrea,Adam Ben Rohrlach,Adam Ben Rohrlach,Christina Warinner,Christina Warinner,Choongwon Jeong,Choongwon Jeong,Philipp W. Stockhammer,Philipp W. Stockhammer,Wolfgang Haak,Johannes Krause +32 more
TL;DR: It is found that 6th millennium BCE populations of North/Central Anat Turkey and the Southern Caucasus shared mixed ancestry on a genetic cline that formed during the Neolithic between Western Anatolia and regions in today's Southern Caucasus/Zagros.
Journal ArticleDOI
Ten millennia of hepatitis B virus evolution
Arthur Kocher,Luka Papac,Rodrigo Barquera,Felix M. Key,Maria A. Spyrou,Maria A. Spyrou,Ron Hübler,Adam Ben Rohrlach,Adam Ben Rohrlach,Franziska Aron,Raphaela Stahl,Antje Wissgott,Florian van Bömmel,Maria Pfefferkorn,Alissa Mittnik,Alissa Mittnik,Vanessa Villalba-Mouco,Vanessa Villalba-Mouco,Gunnar U. Neumann,Maïté Rivollat,Maïté Rivollat,Marieke Sophia van de Loosdrecht,Kerttu Majander,Kerttu Majander,Rezeda I. Tukhbatova,Rezeda I. Tukhbatova,Lyazzat Musralina,Ayshin Ghalichi,Sandra Penske,Susanna Sabin,Megan Michel,Megan Michel,Joscha Gretzinger,Elizabeth A. Nelson,Tiago Ferraz,Tiago Ferraz,Kathrin Nägele,Cody E. Parker,Cody E. Parker,Marcel Keller,Marcel Keller,Evelyn K. Guevara,Evelyn K. Guevara,Michal Feldman,Michal Feldman,Stefanie Eisenmann,Eirini Skourtanioti,Karen Giffin,Guido Alberto Gnecchi-Ruscone,Susanne Friederich,Vittoria Schimmenti,Valery Khartanovich,Marina K. Karapetian,Mikhail S. Chaplygin,Vladimir V. Kufterin,Aleksandr Khokhlov,Andrey A. Chizhevsky,Dmitry A. Stashenkov,Anna F. Kochkina,Cristina Tejedor-Rodríguez,Íñigo García-Martínez de Lagrán,Héctor Arcusa-Magallón,Rafael Garrido-Pena,José I. Royo-Guillén,Jan Nováček,Stéphane Rottier,Sacha Kacki,Sacha Kacki,Sylvie Saintot,Elena Kaverzneva,Andrej B. Belinskiy,Petr Velemínský,Petr Limburský,Michal Kostka,Louise Loe,Elizabeth Popescu,Rachel Clarke,Alice Lyons,Richard Mortimer,Antti Sajantila,Yadira Chinique de Armas,Silvia Teresita Hernández Godoy,Diana Iraíz Hernández-Zaragoza,Jessica Pearson,Didier Binder,Philippe Lefranc,Anatoly R. Kantorovich,Vladimir E. Maslov,Luca Lai,Luca Lai,Magdalena Zoledziewska,Jessica Beckett,Michaela Langová,Alžbeta Danielisová,Tara Ingman,Gabriel García Atiénzar,Maria Paz Miguel de Ibáñez,Alejandro Romero,Alessandra Sperduti,Sophie Beckett,Sophie Beckett,Susannah J. Salter,Emma D. Zilivinskaya,Dmitry V. Vasilev,Kristin von Heyking,Richard L. Burger,Lucy C. Salazar,Luc Amkreutz,Masnav Navruzbekov,Eva Rosenstock,Carmen Alonso-Fernández,Vladimir Slavchev,Alexey Kalmykov,Biaslan Ch. Atabiev,Elena Batieva,Micaela Alvarez Calmet,Bastien Llamas,Bastien Llamas,Michael Schultz,Raiko Krauß,Javier Jimenez-Echevarria,Michael Francken,Svetlana Shnaider,Peter de Knijff,Eveline Altena,Katrien Van de Vijver,Katrien Van de Vijver,Lars Fehren-Schmitz,Tiffiny A. Tung,Sandra Lösch,Maria V. Dobrovolskaya,Nikolaj Makarov,Christopher Read,Melanie Van Twest,Claudia Sagona,Peter C. Ramsl,Murat Akar,K. Aslıhan Yener,Eduardo Carmona Ballestero,Francesco Cucca,Vittorio Mazzarello,Pilar Utrilla,Kurt Rademaker,Eva Fernández-Domínguez,Douglas Baird,Patrick Semal,Lourdes Marquez-Morfin,Mirjana Roksandic,Mirjana Roksandic,Hubert Steiner,Domingo C. Salazar-García,Domingo C. Salazar-García,Domingo C. Salazar-García,Natalia Shishlina,Yılmaz Selim Erdal,Fredrik Hallgren,Yavor Boyadzhiev,Kamen Boyadzhiev,Mario Küßner,Duncan Sayer,Päivi Onkamo,Päivi Onkamo,Robin Skeates,Manuel Rojo-Guerra,Alexandra P. Buzhilova,Elmira Khussainova,Leyla B. Djansugurova,Arman Z. Beisenov,Zainolla Samashev,Ken Massy,Marcello A. Mannino,Marcello A. Mannino,Vyacheslav Moiseyev,Kristiina Mannermaa,Oleg Balanovsky,Marie-France Deguilloux,Sabine Reinhold,Svend Hansen,Egor Kitov,Miroslav Dobeš,Michal Ernée,Harald Meller,Kurt W. Alt,Kurt W. Alt,Kay Prüfer,Christina Warinner,Christina Warinner,Stephan Schiffels,Philipp W. Stockhammer,Philipp W. Stockhammer,Kirsten I. Bos,Cosimo Posth,Cosimo Posth,Alexander Herbig,Wolfgang Haak,Wolfgang Haak,Johannes Krause,Denise Kühnert +197 more
TL;DR: In this article, the Max Planck Society, the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program (771234-PALEoRIDER, to W.H., 805268-CoDisEASe to K. Bos; 834616-ARCHCAUCASUS to S.H. and AP08857177 to A.Z.
Journal ArticleDOI
Using Y-chromosome capture enrichment to resolve haplogroup H2 shows new evidence for a two-path Neolithic expansion to Western Europe.
Adam Ben Rohrlach,Adam Ben Rohrlach,Luka Papac,Ainash Childebayeva,Maïté Rivollat,Maïté Rivollat,Vanessa Villalba-Mouco,Vanessa Villalba-Mouco,Gunnar U. Neumann,Sandra Penske,Eirini Skourtanioti,Marieke Sophia van de Loosdrecht,Murat Akar,Kamen Boyadzhiev,Yavor Boyadzhiev,Marie-France Deguilloux,Miroslav Dobeš,Yılmaz Selim Erdal,Michal Ernée,Marcella Frangipane,Mirosław Furmanek,Susanne Friederich,Emmanuel Ghesquière,Agata Hałuszko,Svend Hansen,Mario Küßner,Marcello A. Mannino,Rana Özbal,Sabine Reinhold,Stéphane Rottier,Domingo C. Salazar-García,Domingo C. Salazar-García,Domingo C. Salazar-García,J. S. Díaz,Philipp W. Stockhammer,Philipp W. Stockhammer,Consuelo Roca de Togores Muñoz,K. Aslıhan Yener,Cosimo Posth,Cosimo Posth,Johannes Krause,Alexander Herbig,Wolfgang Haak,Wolfgang Haak +43 more
TL;DR: The Max Planck Society, the French and German Research Foundations under the INTERACT project (ANR-17-FRAL-0010, DFG-HA-5407/4-1, 2018-2021) to M.R. and W.H., the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program under Grant agreement no. 771234-PALEoRIDER to W.E.S. as discussed by the authors, and the project RVO 67985912 of the Institute of Archaeology of the
Posted ContentDOI
Using Y-chromosome capture enrichment to resolve haplogroup H2 shows new evidence for a two-Path Neolithic expansion to Western Europe
Adam Ben Rohrlach,Adam Ben Rohrlach,Luka Papac,Ainash Childebayeva,Maïté Rivollat,Maïté Rivollat,Vanessa Villalba-Mouco,Gunnar U. Neumann,Sandra Penske,Eirini Skourtanioti,Marieke Sophia van de Loosdrecht,Murat Akar,Kamen Boyadzhiev,Yavor Boyadzhiev,Marie-France Deguilloux,Miroslav Dobeš,Yılmaz Selim Erdal,Michal Ernée,Marcella Frangipane,Mirosław Furmanek,Susanne Friederich,Emmanuel Ghesquière,Agata Hałuszko,Svend Hansen,Mario Küßner,Marcello A. Mannino,Rana Özbal,Sabine Reinhold,Stéphane Rottier,Domingo C. Salazar-García,Domingo C. Salazar-García,Domingo C. Salazar-García,J. S. Díaz,Philipp W. Stockhammer,Philipp W. Stockhammer,Consuelo Roca de Togores Muñoz,K. Aslıhan Yener,Cosimo Posth,Cosimo Posth,Johannes Krause,Alexander Herbig,Wolfgang Haak,Wolfgang Haak +42 more
TL;DR: It is shown that compared to low-coverage shotgun sequencing and 1240K capture, YMCA significantly improves the coverage and number of sites hit on the NRY, increasing the number of Y-haplogroup informative SNPs, and allowing for the identification of previously undiscovered variants.