@article {722421,
	title = {The case of an 85-year old woman with subacute onset of bilateral chorea.},
	journal = {Interactive Annals of Clinical and Translational Neurology},
	volume = {39},
	year = {2024},
	url = {https://interactn.org/2024/03/25/case-39-case-of-an-85-year-old-woman-with-subacute-onset-of-bilateral-chorea/},
	author = {Nakatsuka, Nathan and Vihang Nakhate and Daniel Harrison and Kristin Galetta and Abby Olsen}
}
@article {721956,
	title = {A noncoding regulatory variant in IKZF1 increases acute lymphoblastic leukemia risk in Hispanic/Latino children  },
	journal = {Cell Genomics},
	year = {2024},
	abstract = {Hispanic/Latino children have the highest risk of acute lymphoblastic leukemia (ALL) in the US compared to other racial/ethnic groups, yet the basis of this remains incompletely understood. Through genetic fine-mapping analyses, we identified a new independent childhood ALL risk signal near\&nbsp;IKZF1\&nbsp;in self-reported Hispanic/Latino individuals, but not in non-Hispanic White individuals, with an effect size of \~{}1.44 (95\% confidence interval\&nbsp;= 1.33{\textendash}1.55) and a risk allele frequency of \~{}18\% in Hispanic/Latino populations and \&lt;0.5\% in European populations. This risk allele was positively associated with Indigenous American ancestry, showed evidence of selection in human history, and was associated with reduced\&nbsp;IKZF1\&nbsp;expression. We identified a putative causal variant in a downstream enhancer that is most active in pro-B cells and interacts with the\&nbsp;IKZF1\&nbsp;promoter. This variant disrupts IKZF1 autoregulation at this enhancer and results in reduced enhancer activity in B cell progenitors. Our study reveals a genetic basis for the increased ALL risk in Hispanic/Latino children.},
	url = {https://www.sciencedirect.com/science/article/pii/S2666979X24000685?via\%3Dihub},
	author = {Adam de Smith and Lara Wahlster and Soyoung Jeon and Linda Kachuri and Susan Black and Jalen Langie and Liam Cato and Nakatsuka, Nathan and Tsz-Fung Chan and Guangze Xia and Soumyaa Mazumder and Wenjian Yang and Gazal, Steven and Eng, Celeste and Hu, Donglei and Esteban G. Burchard and Ziv, Elad and Catherine Metayer and Nicholas Mancuso and Jun J Yang and Xiaomei Ma and Joseph L Wiemels and Fulong Yu and Charleston Chiang and Vijay Sankaran}
}
@article {721951,
	title = {Recombination map tailored to Native Hawaiians may improve robustness of genomic scans for positive selection},
	journal = {Human Genetics},
	volume = {143},
	number = {1},
	year = {2024},
	pages = {85-99},
	abstract = {Recombination events establish the patterns of haplotypic structure in a population and estimates of recombination rates are used in several downstream population and statistical genetic analyses. Using suboptimal maps from distantly related populations may reduce the efficacy of genomic analyses, particularly for underrepresented populations such as the Native Hawaiians. To overcome this challenge, we constructed recombination maps using genome-wide array data from two study samples of Native Hawaiians: one reflecting the current admixed state of Native Hawaiians (NH map) and one based on individuals of enriched Polynesian ancestries (PNS map) with the potential to be used for less admixed Polynesian populations such as the Samoans. We found the recombination landscape to be less correlated with those from other continental populations (e.g. Spearman{\textquoteright}s rho = 0.79 between PNS and CEU (Utah residents with Northern and Western European ancestry) compared to 0.92 between YRI (Yoruba in Ibadan, Nigeria) and CEU at 50\&nbsp;kb resolution), likely driven by the unique demographic history of the Native Hawaiians. PNS also shared the fewest recombination hotspots with other populations (e.g. 8\% of hotspots shared between PNS and CEU compared to 27\% of hotspots shared between YRI and CEU). We found that downstream analyses in the Native Hawaiian population, such as local ancestry inference, imputation, and IBD segment and relatedness detections, would achieve similar efficacy when using the NH map compared to an omnibus map. However, for genome scans of adaptive loci using integrated haplotype scores, we found several loci with apparent genome-wide significant signals (|Z-score|\&gt; 4) in Native Hawaiians that would not have been significant when analyzed using NH-specific maps. Population-specific recombination maps may therefore improve the robustness of haplotype-based statistics and help us better characterize the evolutionary history that may underlie Native Hawaiian-specific health conditions that persist today.},
	url = {https://link.springer.com/article/10.1007/s00439-023-02625-2},
	author = {Bryan Dinh and Echo Tang and Kekoa Taparra and Nakatsuka, Nathan and Chen, Fei and Charleston Chiang}
}
@article {713006,
	title = {Genetic continuity and change among the Indigenous peoples of California},
	journal = {Nature},
	year = {2023},
	abstract = {Before the colonial period, California harboured more language variation than all of Europe, and linguistic and archaeological analyses have led to many hypotheses to explain this diversity. We report genome-wide data from 79 ancient individuals from California and 40 ancient individuals from Northern Mexico dating to 7,400{\textendash}200 years before present (BP). Our analyses document long-term genetic continuity between people living on the Northern Channel Islands of California and the adjacent Santa Barbara mainland coast from 7,400 years BP\&nbsp;to modern Chumash groups represented by individuals who lived around 200 years BP. The distinctive genetic lineages that characterize present-day and ancient people from Northwest Mexico increased in frequency in Southern and Central California by 5,200 years BP, providing evidence for northward migrations that are candidates for spreading Uto-Aztecan languages before the dispersal of maize agriculture from Mexico. Individuals from Baja California share more alleles with the earliest individual from Central California in the dataset than with later individuals from Central California, potentially reflecting an earlier linguistic substrate, whose impact on local ancestry was diluted by later migrations from inland regions. After 1,600 years BP, ancient individuals from the Channel Islands lived in communities with effective sizes similar to those in pre-agricultural Caribbean and Patagonia, and smaller than those on the California mainland and in sampled regions of Mexico.},
	url = {https://www.nature.com/articles/s41586-023-06771-5},
	author = {Nakatsuka, Nathan and Brian Holguin and Jakob Sedig and Paul E. Langenwalter II and John Carpenter and Brendan J. Culleton and Cristina Garc{\'\i}a-Moreno and Thomas K. Harper and Debra Martin and J{\'u}piter Mart{\'\i}nez-Ram{\'\i}rez and Antonio Porcayo-Michelini and Vera Tiesler and M. Elisa Villapando-Canchola and Alejandro Valdes Herrera and Kim Callan and Elizabeth Curtis and Aisling Kearns and Lora Iliev and Lawson, Ann Marie and Mah, Matthew and Mallick, Swapan and Adam Micco and Michel, Megan and J. Noah Workman and Oppenheimer, Jonas and Lijun Qiu and Zalzala, Fatma and Rohland, Nadin and Jose Luis Punzo Diaz and John R. Johnson and Reich, David}
}
@article {692522,
	title = {Life and death in early colonial Campeche: new insights from ancient DNA},
	journal = {Antiquity},
	volume = {96},
	number = {388},
	year = {2022},
	pages = {937-954},
	abstract = {Campeche, one of the Spanish Empire{\textquoteright}s main Mexican ports, was a place where previously distinct cultures and populations intermingled during the colonial era (AD 1540{\textendash}1680). Investigation of the town{\textquoteright}s central plaza revealed a Hispanic cemetery of multi-ethnic burials. The authors combine previous analyses with newly generated genome-wide data from 10 individuals to trace detailed life histories of the mostly young, local Indigenous Americans and first-generation European and African immigrants, none of whom show evidence of genetic admixture. These results provide insights into the individual lives and social divides of the town{\textquoteright}s founder communities and demonstrate how ancient DNA analyses can contribute to understanding early colonial encounters.},
	url = {https://www.cambridge.org/core/journals/antiquity/article/life-and-death-in-early-colonial-campeche-new-insights-from-ancient-dna/1E92D867436AD6C150B52FC46A0915F1},
	author = {V. Tiesler and Sedig, J. and Nakatsuka, N. and Mallick, S. and Lazaridis, I. and Bernardos, R. and Broomandkhoshbacht, N. and Oppenheimer, J. and A. M. Lawson and Stewardson, K. and Rohland, N. and Kennett, D. and T. D. Price and Reich, D.}
}
@article {683476,
	title = {Ethics of DNA research on human remains: five globally applicable guidelines},
	journal = {Nature},
	volume = {599},
	number = {7883},
	year = {2021},
	pages = {41-46},
	abstract = {We are a group of archaeologists, anthropologists, curators and geneticists representing diverse global communities and 31 countries. All of us met in a virtual workshop dedicated to ethics in ancient DNA research held in November 2020. There was widespread agreement that globally applicable ethical guidelines are needed, but that recent recommendations grounded in discussion about research on human remains from North America are not always generalizable worldwide. Here we propose the following globally applicable guidelines, taking into consideration diverse contexts. These hold that: (1) researchers must ensure that all regulations were followed in the places where they work and from which the human remains derived; (2) researchers must prepare a detailed plan prior to beginning any study; (3) researchers must minimize damage to human remains; (4) researchers must ensure that data are made available following publication to allow critical re-examination of scientific findings; and (5) researchers must engage with other stakeholders from the beginning of a study and ensure respect and sensitivity to stakeholder perspectives. We commit to adhering to these guidelines and expect they will promote a high ethical standard in DNA research on human remains going forward.},
	url = {https://www.nature.com/articles/s41586-021-04008-x},
	author = {Alpaslan-Roodenberg,S. and (33 authors) and Nakatsuka, N. and (28 authors) and Zahir, M.}
}
@article {683475,
	title = {Ancient genomes reveal long range influence of the site and culture of Tiwanaku},
	journal = {Science Advances},
	volume = {7},
	number = {39},
	year = {2021},
	abstract = {Tiwanaku civilization flourished in the Lake Titicaca basin between 500 and 1000 CE and at its apogee influenced wide areas across the southern Andes. Despite a considerable amount of archaeological data, little is known about the Tiwanaku population. We analyzed 17 low-coverage genomes from individuals dated between 300 and 1500 CE and demonstrated genetic continuity in the Lake Titicaca basin throughout this period, which indicates that the substantial cultural and political changes in the region were not accompanied by large-scale population movements. Conversely, the ritual center of Tiwanaku revealed high diversity, including individuals with primarily local genetic ancestry and those with foreign admixture or provenance from as far as the Amazon. Nonetheless, most human offerings associated with the Akapana platform exhibited pure Titicaca basin ancestry and dated to ca. 950 CE{\textemdash}the onset of Tiwanaku{\textquoteright}s decline as a sociopolitical center. Our results strengthen the view of Tiwanaku as a complex and far-reaching polity.},
	url = {https://www.science.org/doi/10.1126/sciadv.abg7261?url_ver=Z39.88-2003\&rfr_id=ori:rid:crossref.org\&rfr_dat=cr_pub\%20\%200pubmed},
	author = {Popovic, D. and Molak, M. and Ziolkowski, M. and Vranich, A. and Sobczyk, M. and Vidaurre, D. and Agresti, G. and Skrzypczak, M. and Ginalski, K. and Lamnidis, T. and Nakatsuka, N. and Mallick, S. and Baca, M.}
}
@article {664506,
	title = {Two Genetic Variants Explain the Association of European Ancestry with Multiple Sclerosis Risk in African-Americans},
	journal = {Scientific Reports},
	volume = {10},
	number = {1},
	year = {2020},
	pages = {16902},
	abstract = {Epidemiological studies have suggested differences in the rate of multiple sclerosis (MS) in individuals of European ancestry compared to African ancestry, motivating genetic scans to identify variants\&nbsp;that could contribute to such patterns. In a whole-genome scan in 899 African-American cases and 1155 African-American controls, we confirm that African-Americans who inherit segments of the genome of European ancestry at a chromosome 1 locus are at increased risk for MS [logarithm of odds (LOD) = 9.8], although the signal weakens when adding an additional 406 cases, reflecting heterogeneity in the two sets of cases [logarithm of odds (LOD) = 2.7]. The association in the 899 individuals can be fully explained by two variants previously associated with MS in European ancestry individuals. These variants tag a MS susceptibility haplotype associated with decreased CD58 gene expression (odds ratio of 1.37; frequency of 84\% in Europeans and 22\% in West Africans for the tagging variant) as well as another haplotype near the FCRL3 gene (odds ratio of 1.07; frequency of 49\% in Europeans and 8\% in West Africans). Controlling for all other genetic and environmental factors, the two variants predict a 1.44-fold higher rate of MS in European-Americans compared to African-Americans.},
	url = {https://www.nature.com/articles/s41598-020-74035-7},
	author = {Nakatsuka, Nathan and Patterson, Nick and Nikolaos Patsopoulos and Nicholas Altemose and Tandon, Arti and Ashley Beecham and Jacob McCauley and Noriko Isobe and Stephen Hauser and Philiip De Jager and David Hafler and Oksenberg, Jorge and Reich, David}
}
@article {662494,
	title = {ContamLD: estimation of ancient nuclear DNA contamination using breakdown of linkage disequilibrium},
	journal = {Genome Biology},
	volume = {21},
	number = {1},
	year = {2020},
	pages = {199},
	abstract = {We report a method called ContamLD for estimating autosomal ancient DNA (aDNA) contamination by measuring the breakdown of linkage disequilibrium in a sequenced individual due to the introduction of contaminant DNA. ContamLD leverages the idea that contaminants should have haplotypes uncorrelated to those of the studied individual. Using simulated data, we confirm that ContamLD accurately infers contamination rates with low standard errors: for example, less than 1.5\% standard error in cases with less than 10\% contamination and 500,000 sequences covering SNPs. This method is optimized for application to aDNA, taking advantage of characteristic aDNA damage patterns to provide calibrated contamination estimates, and is available at https://github.com/nathan-nakatsuka/ContamLD.},
	url = {https://genomebiology.biomedcentral.com/articles/10.1186/s13059-020-02111-2},
	author = {Nathan Nakatsuka* and Harney*, {\'E}adaoin and Mallick, Swapan and Mah, Matthew and Patterson, Nick and Reich, David}
}
@article {662492,
	title = {Integration of ancient DNA with transdisciplinary dataset finds strong support for Inca resettlement in the south Peruvian coast},
	journal = {PNAS},
	volume = {117},
	number = {31},
	year = {2020},
	pages = {18359-18368},
	abstract = {Ancient DNA (aDNA) analysis provides a powerful means of investigating human migration, social organization, and a plethora of other crucial questions about humanity{\textquoteright}s past. Recently, specialists have suggested that the ideal research design involving aDNA would include multiple independent lines of evidence. In this paper, we adopt a transdisciplinary approach integrating aDNA with archaeological, biogeochemical, and historical data to investigate six individuals found in two cemeteries that date to the Late Horizon (1400 to 1532 CE) and Colonial (1532 to 1825 CE) periods in the Chincha Valley of southern Peru. Genomic analyses indicate that these individuals are genetically most similar to ancient and present-day populations from the north Peruvian coast located several hundred kilometers away. These genomic data are consistent with 16th century written records as well as ceramic, textile, and isotopic data. These results provide some of the strongest evidence yet of state-sponsored resettlement in the pre-Colonial Andes. This study highlights the power of transdisciplinary research designs when using aDNA data and sets a methodological standard for investigating ancient mobility in complex societies.},
	url = {https://www.pnas.org/content/117/31/18359.long},
	author = {Jacob L Bongers and Nakatsuka, Nathan and Colleen O{\textquoteright}Shea and Harper, Thomas K and Henry Tantale{\'a}n and Charles Stanish and Lars Fehren-Schmitz}
}
@article {662493,
	title = {Ancient genomes in South Patagonia reveal population movements associated with technological shifts and geography},
	journal = {Nature Communications},
	volume = {11},
	number = {1},
	year = {2020},
	pages = {3868},
	abstract = {Archaeological research documents major technological shifts among people who have lived in the southern tip of South America (South Patagonia) during the last thirteen millennia, including the development of marine-based economies and changes in tools and raw materials. It has been proposed that movements of people spreading culture and technology propelled some of these shifts, but these hypotheses have not been tested with ancient DNA. Here we report genome-wide data from 20 ancient individuals, and co-analyze it with previously reported data. We reveal that immigration does not explain the appearance of marine adaptations in South Patagonia. We describe partial genetic continuity since ~6600 BP and two later gene flows correlated with technological changes: one between 4700{\textendash}2000 BP that affected primarily marine-based groups, and a later one impacting all \&lt;2000 BP groups. From ~2200{\textendash}1200 BP, mixture among neighbors resulted in a cline correlated to geographic ordering along the coast.},
	url = {https://www.nature.com/articles/s41467-020-17656-w},
	author = {Nathan Nakatsuka* and Pierre Luisi* and Josefina M B Motti and M{\'o}nica Salemme and Fernando Santiago and Manuel D D{\textquoteright}Angelo Del Campo and Rodrigo J Vecchi and Yolanda Espinosa-Parrilla and Alfredo Prieto and Adamski, Nicole and Lawson, Ann Marie and Harper, Thomas K and Culleton, Brendan J and Kennett, Douglas J and Lalueza-Fox, Carles and Mallick, Swapan and Rohland, Nadin and Ricardo A Guich{\'o}n and Graciela S Cabana and Rodrigo Nores and Reich, David}
}
@article {662491,
	title = {A Paleogenomic Reconstruction of the Deep Population History of the Andes},
	journal = {Cell},
	volume = {181},
	number = {5},
	year = {2020},
	pages = {1131-1145},
	abstract = {There are many unanswered questions about the population history of the Central and South Central Andes, particularly regarding the impact of large-scale societies, such as the Moche, Wari, Tiwanaku, and Inca. We assembled genome-wide data on 89 individuals dating from \~{}9,000-500 years ago (BP), with a particular focus on the period of the rise and fall of state societies. Today{\textquoteright}s genetic structure began to develop by 5,800 BP, followed by bi-directional gene flow between the North and South Highlands, and between the Highlands and Coast. We detect minimal admixture among neighboring groups between \~{}2,000-500 BP, although we do detect cosmopolitanism (people of diverse ancestries living side-by-side) in the heartlands of the Tiwanaku and Inca polities. We also highlight cases of long-range mobility connecting the Andes to Argentina and the Northwest Andes to the Amazon Basin. https://www.youtube.com/watch?v=S-ra2eDF16U},
	url = {https://www.cell.com/cell/fulltext/S0092-8674(20)30477-3?_returnURL=https\%3A\%2F\%2Flinkinghub.elsevier.com\%2Fretrieve\%2Fpii\%2FS0092867420304773\%3Fshowall\%3Dtrue},
	author = {Nakatsuka, Nathan and Lazaridis, Iosif and Chiara Barbieri and Skoglund, Pontus and Rohland, Nadin and Mallick, Swapan and Posth, Cosimo and Kelly Harkins-Kinkaid and Ferry, Matthew and Harney, {\'E}adaoin and Michel, Megan and Stewardson, Kristin and Jannine Novak-Forst and Jos{\'e} M Capriles and Marta Alfonso Durruty and Karina Aranda {\'A}lvarez and David Beresford-Jones and Richard Burger and Lauren Cadwallader and Ricardo Fujita and Johny Isla and George Lau and Carlos L{\'e}muz Aguirre and Steven LeBlanc and Sergio Calla Maldonado and Frank Meddens and Pablo G Messineo and Culleton, Brendan J and Harper, Thomas K and Jeffrey Quilter and Gustavo Politis and Kurt Rademaker and Markus Reindel and Mario Rivera and Lucy Salazar and Jos{\'e} R Sandoval and Calogero M Santoro and Nahuel Scheifler and Vivien Standen and Maria Ines Barreto and Isabel Flores Espinoza and Elsa Tomasto-Cagigao and Guido Valverde and Kennett, Douglas J and Alan Cooper and Krause, Johannes and Haak, Wolfgang and Llamas, Bastien and Reich, David and Lars Fehren-Schmitz}
}
@article {642195,
	title = {The formation of human populations in South and Central Asia.},
	journal = {Science},
	volume = {365},
	number = {6457},
	year = {2019},
	url = {https://science.sciencemag.org/content/365/6457/eaat7487.long},
	author = {Narasimhan*, V. and Patterson*, N. and Moorjani+, P. and Rohland+, N. and Bernardos, R. and Mallick, S. and Lazaridis, I. and Nakatsuka, N. and [104 authors] and Boivin, N. and Thangaraj+, K. and Kennett+, D. and Frachetti+, M. and Pinhasi+, R. and Reich+, D.}
}
@article {642344,
	title = {An Ancient Genome from the Indus Valley Civilization Lacks Ancestry from Steppe Pastoralists or Western Iranian Farmers},
	journal = {Cell},
	volume = {8674},
	number = {19},
	year = {2019},
	pages = {30967-5},
	url = {https://www.sciencedirect.com/science/article/pii/S0092867419309675?via\%3Dihub},
	author = {Shinde*, V. and Narasimhan*, V. and Rohland, N. and Mallick, S. and Mah, M. and Lipson, M. and Nakatsuka, N. and [19 authors] and Rai+, N. and Reich+, D.}
}
@article {642194,
	title = {Reconstructing the Deep Population History of Central and South America},
	journal = {Cell},
	volume = {175},
	number = {5},
	year = {2018},
	pages = {1185-1197},
	url = {https://www.sciencedirect.com/science/article/pii/S0092867418313801?via\%3Dihub},
	author = {Posth*, C. and Nakatsuka*, N. and Lazaridis, I. and Skoglund, P. and Mallick, S. and Lamnidis, T. and Rohland, N. and Nagele, K. and Adamski, N. and Bertolini, E. and Broomandkhoshbacht, N. and Cooper, A. and Culleton, B. and Ferraz, T. and Ferry, M. and Furtwangler, A. and Haak, W. and Harkins, K. and Harper, T. and Hunemeier, T. and Lawson, A. and Llamas, B. and Michel, M. and E. Nelson and Oppenheimer, J. and Patterson, N. and Schiffels, S. and Sedig, J. and Stewardson, K. and Talamo, S. and Wang, C. and Hublin, J. and Hubbe, M. and Harvati, K. and Nuevo Delaunay, A. and Beier, J. and Francken, M. and Kaulicke, P. and Reyes-Centeno, H. and Rademaker, K. and Trask, W. and Robinson, M. and Gutierrez, S. and Prufer, K. and Salazar-Garcia, D. and Chim, E. and Muller Plumm Gomes, L. and Alves, M. and Liryo, A. and Inglez, M. and Oliveira, R. and Bernardo, D. and Barioni, A. and Wesolowski, V. and Scheifler, N. and Rivera, M. and Plens, C. and Messineo, P. and Figuti, L. and Corach, D. and Scabuzzo, C. and Eggers, S. and DeBlasis, P. and Reindel, M. and Mendez, C. and Politis, G. and Tomasto-Cagigao, E. and Kennett, D. and Strauss, A. and Fehren-Schmitz, L. and Krause, J. and Reich, D.}
}
@article {642193,
	title = {A framework for enhancing ethical genomic research with indigenous communities},
	journal = {Nature Communications},
	volume = {9},
	number = {1},
	year = {2018},
	pages = {2957},
	url = {https://www.ncbi.nlm.nih.gov/pubmed/30054469},
	author = {Claw, K. and Anderson, M. and Begay, R. and Tsosie, K. and Fox, K. and Garrison, N. and the Summer internship for INdigenous peoples in Genomics (SING) Consortium}
}
@article {642192,
	title = {Advancing the ethics of paleogenomics.},
	journal = {Science: Policy Forum},
	volume = {360},
	number = {6387},
	year = {2018},
	pages = {384-385},
	url = {https://science.sciencemag.org/content/360/6387/384.long},
	author = {Bardill, J. and Bader, A. and Garrison, N. and Bolnick, D. and Raff, J. and Walker, A. and Malhi, R. and the Summer Internship for INdigenous peoples in Genomics (SING) Consortium}
}
@article {642191,
	title = {The Promise of Discovering Population-Specific Disease-Associated Genes in South Asia.},
	journal = {Nature Genetics},
	volume = {49},
	number = {9},
	year = {2017},
	pages = {1403-1407},
	url = {https://www.nature.com/articles/ng.3917},
	author = {Nakatsuka, N. and Moorjani, P. and Rai, N. and Sarkar, B. and Tandon, A. and Patterson, N. and Bhavani, G. and Girisha, K. and Mustak, N. and Srinivasan, S. and Kaushik, A. and Vahab, S. and Jagadeesh, S. and Satyamoorthy, K. and Singh, L. and Reich+, D. and Thangaraj+, K.}
}
@article {642040,
	title = {CLYBL is a polymorphic human enzyme with malate synthase and β-methylmalate synthase activity.},
	journal = {Human Molecular Genetics},
	volume = {23},
	number = {9},
	year = {2014},
	pages = {2313-23},
	url = {https://academic.oup.com/hmg/article/23/9/2313/632255},
	author = {Strittmatter, L. and Li, Y. and Nakatsuka, N. and Calvo, S. and Grabarek, Z. and Mootha, V.}
}
@article {642039,
	title = {Identifying the Unique Challenges Facing Kanaka Maoli Kupuna Residing Outside of Hawai'i.},
	journal = {Hulili Journal for Multidisciplinary Research on Hawaiian Well-Being},
	volume = {9},
	year = {2013},
	pages = {133-151},
	author = {Nakatsuka, N. and Esquivel, L. and Levin, M. and Browne, C. and Braun, K.}
}
@article {642037,
	title = {Factors influencing the degradation of archival formalin-fixed paraffin-embedded tissue sections},
	journal = {Journal of Histochemistry and Cytochemistry},
	volume = {59},
	number = {4},
	year = {2011},
	pages = {356-65},
	url = {https://journals.sagepub.com/doi/full/10.1369/0022155411398488?url_ver=Z39.88-2003\&rfr_id=ori\%3Arid\%3Acrossref.org\&rfr_dat=cr_pub\%3Dpubmed},
	author = {Xie, R. and Chung, J. and Ylaya, K. and Williams, R. and Guerrero, N. and Nakatsuka, N. and Badie, C. and Hewitt, S.}
}
