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1 l populations (European, Asian, African, and Native American).
2 black, Asian/Pacific Islander, Hispanic, and Native American.
3 were Hispanic; 13, African; 8, white; and 2, Native American.
4 ncidence was highest in blacks and lowest in Native Americans.
5 landers than to any present-day Eurasians or Native Americans.
6 he Ainu and Polynesians than he is to modern Native Americans.
7 ia and were directly related to contemporary Native Americans.
8 tion directly ancestral to many contemporary Native Americans.
9 he primary sources of health problems facing Native Americans.
10 tics in the risk for substance dependence in Native Americans.
11 3.3 for Asian/Pacific Islanders and 3.1 for native Americans.
12 iberia and a possible homeland for ancestral Native Americans.
13 pe-specific invasive disease potential among Native Americans.
14 substantially lower for blacks, Asians, and Native Americans.
15 precise time estimates for the emergence of Native Americans.
16 amined in skeletal muscle of 153 nondiabetic Native Americans.
17 ssociation both in Finns and in Southwestern Native Americans.
18 ultimorbidity network followed by Whites and Native Americans.
19 scent populations but not among Europeans or Native Americans.
20 equency in modern Asians, Australasians, and Native Americans.
21 1 [0.021-0.022]; Asian: 0.037 [0.036-0.039]; Native American: 0.010 [0.0076-0.013]), lower quartile h
22 ents were black, 2% were Hispanic, 0.3% were Native American, 1% were Asian, and 90% were white, resp
24 ), white (14.0% and 32.6%, respectively) and Native American (19.2% and 43.4%, respectively), respond
25 P < .001; Asian: 3.16 [2.68-3.73], P < .001; Native American: 2.11 [1.45-3.08], P < .001), lower hous
26 1%) and among non-Hispanic blacks (170%) and Native Americans (241%) compared to non-Hispanic whites
28 mong 27 705 past-year alcohol or drug users, Native Americans (31.5%), adolescents of multiple race/e
29 spanic whites, blacks (-30%), Asians (-19%), Native Americans (-42%), and Hispanics (-29%) all had lo
30 y, whereas the United States' population was Native American 500 years ago but is overwhelmingly Old
31 comparatively prevalent among adolescents of Native American (9.7%) and multiple race/ethnicity (8.8%
33 ed Rapanui, we found statistical support for Native American admixture dating to AD 1280-1495 and Eur
34 t studies have reported genetic evidence for Native American admixture in present-day indigenous inha
35 ere we directly test the hypothesis that the Native American admixture of the current Rapa Nui popula
36 s from islands across Polynesia for signs of Native American admixture, analysing 807 individuals fro
38 ed odds of substance-related disorders among Native Americans, adolescents of multiple race/ethnicity
39 A major factor for the population decline of Native Americans after European contact has been attribu
40 Zea mays ssp. mays) was the primary grain of Native American agricultural systems in the centuries pr
41 Second, this moderating pattern flips for Native Americans, Alaska Natives, Asians, and Hispanics,
43 y, defined as self-reported black, Hispanic, Native American, Alaskan Native, Native Hawaiian, or Pac
45 ely to have occurred after the divergence of Native American ancestors from east Asian ancestors, but
46 al DNA analyses have dated the separation of Native American ancestors from the Asian gene pool to 23
47 an Upper Palaeolithic Mal'ta population into Native American ancestors is also shared by the Anzick-1
48 e-way admixed between European, African, and Native American ancestries and provide an opportunity to
49 the recent mixing of African, European, and Native American ancestries, has resulted in different et
50 admixed population of African, European, and Native American ancestries, have the highest asthma prev
53 ohort (n = 1998) and evaluated the effect of Native American ancestry (NAA) and diet on biomarkers fo
54 th pancreatitis included genetically defined Native American ancestry (P < .001), older age (P < .001
56 d on chromosome 5q35.1, indicating that each Native American ancestry allele was associated with a 0.
58 ciation between local European, African, and Native American ancestry and BDR, adjusting for genomic
59 ombia harbor substantially more European and Native American ancestry as a result of their complex ad
60 s the ancestry, we showed that the choice of Native American ancestry could affect the local ancestry
61 ilobase in segments inferred to have diploid Native American ancestry from the genomes of Mexican and
63 opulations to identify 324 highly predictive Native American ancestry informative markers (AIMs).
66 Furthermore, we estimate that 14 to 38% of Native American ancestry may originate through gene flow
68 s the first study supporting the notion that Native American ancestry significantly contributes to NM
69 age, NMO patients had a higher proportion of Native American ancestry than controls (68.1% vs 58.6%;
71 t 18q21 in Latinos (P = 6.8 x 10(-6)), where Native American ancestry was associated with increased r
72 st significant peak was 6p21.32-p22.1, where Native American ancestry was associated with lower IgE l
74 of genomic variation that co-segregated with Native American ancestry was associated with risk of rel
75 .1) at which local African, European, and/or Native American ancestry was significantly associated wi
76 a genomic region (3p24.2) in which increased Native American ancestry was significantly associated wi
77 higher exposure to asparaginase, and higher Native American ancestry were independent risk factors f
79 sociations with retinopathy were present for Native American ancestry; country of origin; health insu
81 eviously possible, we assembled data from 52 Native American and 17 Siberian groups genotyped at 364,
84 ntributions to the Mestizo FRDA gene pool by Native American and European genes were 76-87% and 13-24
85 are the result of two-way admixture between Native American and European populations or of three-way
86 n resulted from the admixture between mainly Native American and European populations, we used genome
91 a calibrated sequence-based analysis of 222 Native American and relevant Eurasian Y chromosomes (24
92 udicial decisions that Kennewick Man was not Native American and that therefore NAGPRA did not apply.
93 e-grain intake was lowest among youth of the Native American and white races and among youth of high
94 4-h EE measures in 509 healthy subjects (368 Native Americans and 141 whites) while subjects consumed
95 which were spread throughout the Americas by Native Americans and adapted to a wide range of environm
96 ojects: newborn screening for SCID in Navajo Native Americans and B-cell reconstitution in patients w
97 sians, Asian Indians, African Americans, and Native Americans and did not differ by adiponectin assay
98 populations, particularly African Americans, Native Americans and Hispanic Americans, are disproporti
104 arkers in at least 232 new Latino, European, Native American, and African samples, and we selected a
107 tive traits were analyzed in 536 nondiabetic Native Americans, and ASK1 expression was examined in sk
108 en OR = 0.75, 95% CI = 0.58-0.96; Hispanics, Native Americans, and whites showed no significant assoc
109 rn Siberia (such as the Koryaks), as well as Native Americans; and a Holocene migration of other East
111 the recognized maternal founding lineages of Native Americans are at least 15, indicating that the ov
113 Hispanics, Asians and Pacific Islanders, and Native Americans at a higher risk than Whites of being d
115 e = 74.6%, range = 45.0%-96.7%), followed by Native American (average = 18.1%, range = 2.1%-33.3%) an
116 , with Pacific Islanders, Asian Indians, and Native Americans being considerably more prone to develo
117 ng White, African American, Asian, Hispanic, Native American, Bi- or Multi-racial and Pacific Islande
118 tury socioecological fire regimes, including Native American burning, postcontact disruption and nati
122 ent of the isolates in MCG-2 originated from Native American clinics, and 90% belonged to two PFGE ty
125 eta (beta), and theta (theta) EEG power in a Native American cohort of 322 individuals to take advant
127 ical sites spanning approximately 3,500 y of Native American, colonial, and historical occupation.
130 at CA-MRSA in Wisconsin likely originated in Native American communities in the early 1990s and since
134 curring metals in abandoned mine wastes in a Native American community in northeastern Arizona were i
137 rought forward supporting the possibility of Native American contact prior to the European "discovery
138 he northeast Asian affinities of present-day Native Americans contrast with a distinctive morphology
140 pean admixture, but also a contribution from Native Americans dating to 1280-1495 AD, demonstrating e
141 e-climate relationships were strongest after Native American depopulation-following mission establish
142 rn Eurasian genetic signatures in modern-day Native Americans derive not only from post-Columbian adm
144 genome-wide data to show that some Amazonian Native Americans descend partly from a Native American f
145 ociation was greater in Hispanic children of Native American descent (beta=2.3; P=0.004) than in non-
146 ts were replicated in a population sample of Native American descent (top hit rs1611115, P = 4.1 x 10
148 ter their arrival to the Americas, ancestral Native Americans diversified into two basal genetic bran
149 e American groups in South America than with Native Americans elsewhere, providing further support fo
151 status epilepticus, older age, and Black and Native American/Eskimo race; patients admitted to a rura
153 mixture mapping by comparing levels of local Native American, European, and African ancestry between
154 subcontinental source populations within the Native American, European, and African segments of the a
155 ean populations or of three-way admixture of Native American, European, and West African populations.
156 and potentially ancient substructure within Native American, European, and West African source popul
157 erica has been the site of ongoing mixing of Native Americans, European settlers, and Africans (broug
158 ction were both high information content for Native American/European ancestry (measured as the stand
160 portionate contribution of European male and Native American female ancestry to present-day populatio
163 onian Native Americans descend partly from a Native American founding population that carried ancestr
164 we focused our map on markers distinguishing Native American from other ancestries and restricted it
165 tes risk haplotype had a frequency of 50% in Native Americans from Mexico but was rare in Europeans a
167 mixture of European mutant FRDA genes in the Native American gene pool that existed prior to contact
168 at this SNP was highly correlated with local Native American genetic ancestry (P = 1.8 x 10(-8)).
172 ionship and requested repatriation under the Native American Graves Protection and Repatriation Act (
173 pa Nui, between Polynesian individuals and a Native American group most closely related to the indige
176 istently indicated a single common origin of Native American groups from Central and South America.
177 uan individual shares more alleles with some Native American groups in South America than with Native
180 ad a higher incidence of AITL and ENKCL; and Native Americans had a lower incidence of PTCL-NOS (all
181 ith increased risk of ASD, as were Asian and Native American haplogroups A and M, with odds ratios ra
182 will probably increase extensively when all Native American haplogroups reach the same level of phyl
183 lience in oyster populations under long-term Native American harvest, sea-level rise, and climate cha
184 demographic impact of European contact with Native Americans has remained unclear despite recent int
185 teria for a substance-related disorder, with Native Americans having the highest prevalence of use (4
187 different selective pressures in determining Native American HLA diversity, we evaluated the relation
189 a higher likelihood of pregnancy was seen in Native American (HR, 1.77; 95% CI, 1.33 to 2.36), Hispan
191 ense variant (common only in East Asians and Native Americans) in MFSD12, a gene recently associated
192 ated with substance dependence phenotypes in Native Americans include OPRM1, CRN1, COMT, GABRA2, MAOA
193 found that the ancestors of all present-day Native Americans, including Athabascans and Amerindians,
194 t in the etiology of substance dependence in Native Americans, including studies of heritability, lin
195 ricana Medik.), once a staple food source of Native American Indians, produces protein-rich tubers, t
196 toric contact of Polynesian individuals with Native American individuals (around AD 1200) contemporan
197 r was generally greater among men, white and Native American individuals, younger and previously or n
198 ontrolled, randomised trial enrolled healthy Native American infants aged 6 months or younger who wer
199 etic relationship between Palaeo-Eskimos and Native American, Inuit, Yup'ik and Aleut populations rem
200 ewick Man, referred to as the Ancient One by Native Americans, is a male human skeleton discovered in
201 o Native American populations, although most Native Americans lack protective variants seen in other
202 oss between a wild sunflower and a primitive Native American landrace that has not been the target of
206 %; black, 12%; Hispanic, 12%; Asian, 4%; and Native American, < 1%) with neuroblastoma were included.
208 ectional facilities, and among sports teams, Native Americans, men who have sex with men, and militar
209 heories (epistemological orientations) among Native Americans (Menominee) and European American child
212 ation in human STAC3 causes the debilitating Native American myopathy (NAM), but the nature of how St
215 eas expression of Stac3W280S (containing the Native American myopathy mutation) partially restored Ca
217 further genotyped in independent samples of Native American (n = 3,723) and Old Order Amish (n = 486
218 was asserted that Kennewick Man was neither Native American nor closely related to the claimant Plat
219 such dynamics in 19th century, post-contact Native Americans on the western Great Plains is especial
220 The mutation was not carried by the three Native Americans or 360 patients from Asia or the Pacifi
221 ), Asian or Pacific Islander (OR, 3.51), and Native American (OR, 5.22) patients with candidemia were
222 ic white people, and men and women of Asian, Native American, or unkown race/ethnicity who are referr
227 5898099 was replicated in a second sample of Native Americans (P = 0.04, 1.22 [1.01-1.47]), while tha
228 nic blacks, Asians or Pacific Islanders, and Native Americans (P<0.05 for all comparisons) and that t
229 th populations (Finns, P = .01; Southwestern Native Americans, P = .008), and the GABRA6 1519T allele
230 gesic (mean, 7.4; 95% CI, 4.0-10.8) than non-Native American patients (mean, 11.2; 95% CI, 7.2-15.2;
231 score (mean, 6.5; 95% CI, 3.6-9.4) than non-Native American patients (mean, 8.1; 95% CI, 6.3-9.9; t3
232 inpatient mortality benefit was observed for Native American patients (n = 185; OR, 0.38 [95% CI, 0.1
239 for Asian patients, 0.95 (0.52 to 1.73) for Native American patients, and 0.95 (0.60 to 1.50) for pa
240 small population size and limited number of Native American patients, PTCL subtype frequencies in th
241 ce of gene flow from European or present-day Native American peoples, and Inuit living around Hudson
242 estry is not related to any extant Brazilian Native American population already studied, and thus the
243 ical data needed to assess the links between Native American population decline and ecological change
244 trically interviewed samples, a Southwestern Native American population sample (N = 433) and a Finnis
246 nome-wide patterns of African, European, and Native American population structure within and among Hi
250 he Medieval Climate Anomaly (950-1250 CE) as Native American populations adopted intensive maize agri
252 f uniparentally inherited genetic systems in Native American populations and the comparison of these
253 groups as well as the most likely ancestral Native American populations as the ancestry, we showed t
255 g contact between prehistoric Polynesian and Native American populations has long intrigued researche
256 Pre-Columbian (pre-1492 CE), maize-dependent Native American populations in the midcontinental United
258 Analyses of this dataset that focused on Native American populations revealed very strong cluster
259 available African, European, East Asian and Native American populations reveals strong genetic ties
260 ly, we find evidence of a deep divergence in Native American populations that predates the Anzick-1 i
262 e not revealed any risk variants specific to Native American populations, although most Native Americ
266 n American (PR 1.86; 95% CI: 1.42-2.45), and Native American (PR 1.87; 95% CI: 1.48-2.35) race were i
267 , the differences between Paleoamericans and Native Americans probably resulted from in situ evolutio
268 included younger age, male gender, Black or Native American race, a higher burden of medical comorbi
269 d with increasing age, male sex, Asian race, Native American race, and symptoms of weight loss and vo
272 dependence were generally greater among men, Native Americans, respondents aged 18 to 44 years, those
273 g in the staggered abandonment of many major Native American river valley settlements and large urban
274 ), blacks (RR, 1.17; 95% CI, 1.03-1.33), and Native Americans (RR, 1.72; 95% CI, 1.07-2.77) had incre
275 se associations replicated in an independent Native American sample (1.19, P = 0.04, for rs11003125)
278 n the earliest American skeletons and modern Native Americans, separate origins have been postulated
281 dence has a substantial genetic component in Native Americans, similar in magnitude to that reported
282 he maize-based agriculture practiced by many Native American societies in eastern North America at th
285 find that Kennewick Man is closer to modern Native Americans than to any other population worldwide.
286 changes in socioecological systems from the Native American to the current period drove shifts in fi
289 e cannabis use disorder were higher for men, Native Americans, unmarried individuals, those with low
290 d haplotypes in a group of 218 Lacandon Maya Native American using a high-resolution next generation
291 that Y-chromosomal diversity among the first Native Americans was greater than previously recognized.
292 rom the admixture of Europeans, Africans and Native Americans, which started over 400 years ago and h
293 tance use is widespread among adolescents of Native American, white, Hispanic, and multiple race/ethn
294 nd genetically closely related to modern-day Native Americans, with no close affinity to east Asians.
296 wer rates of advanced cancer among Asian and Native American women persisted when the cohort was stra
297 omen were more likely than white, Asian, and Native American women to have large, advanced-stage, hig
299 nificantly more prevalent among men, whites, Native Americans, younger and unmarried adults, and thos