ライフサイエンスコーパス: dizygotic

1 ealthy female twins (150 monozygotic and 366 dizygotic).

2 3 same-sex twin pairs (90 monozygotic and 83 dizygotic).

3 nder, otherwise the twins were considered as dizygotic.

4 dizygotic, 1.59 (+0.18); and (5) male-female dizygotic, 1.39 (+0.11).

5 monozygotic, 3.02 (+0.39); (4) female-female dizygotic, 1.59 (+0.18); and (5) male-female dizygotic,

6 ale monozygotic, 3.29 (+0.37); (2) male-male dizygotic, 1.86 (+0.20); (3) female-female monozygotic,

7 180 male and 1315 female pairs) and same-sex dizygotic (2765 male and 2613 female pairs) twins born f

8 1383 monozygotic (2766 individuals) and 1933 dizygotic (2866 individuals) pairs.

9 ere an absolute 5% (95% CI, 4%-6%) higher in dizygotic (37%; 95% CI, 36%-38%) and an absolute 14% (95

10 concordance rate in monozygotic (28%) versus dizygotic (5%) twins as well as familial recurrence risk

11 r (P = 0.030) in monozygotic (17.2%) than in dizygotic (8.4%) twins, supporting a genetic contributio

12 ed nested co-twin control analyses among 643 dizygotic and 365 monozygotic twin pairs discordant for

13 on of fixations to face and motion, from 536 dizygotic and monozygotic 5-month-old twins in: naturali

14 d the supragingival plaque microbiome of 485 dizygotic and monozygotic twins aged 5-11.

15 profiled supragingival plaque microbiomes of dizygotic and monozygotic twins during 3 visits over 12-

16 ng 16,477 twins (5084 monozygotic and 11,393 dizygotic); and 3) a two-sample Mendelian randomization

17 ale-male twin pairs (708 monozygotic and 490 dizygotic) ascertained from a population-based registry,

18 ing 60 pairs of twins (42 monozygotic and 18 dizygotic; average age, 45.7 +/- 22.1 y; average body ma

19 casian female twins (706 monozygotic and 757 dizygotic), between 24 and 79 years of age, underwent re

20 firmed in schizophrenia and observed between dizygotic, but not monozygotic co-twins discordant for s

21 In 13 986 twins (6181 monozygotic and 7805 dizygotic), cannabis use ranged from 1345 (30.4%) of 443

22 .9% +/- 9.5% compared with 36.4% +/- 9.3% in dizygotic co-twins (P = .11).

23 ignificantly raised risk of breast cancer in dizygotic compared with monozygotic twins younger than 3

24 n-twin concordance (0.91) and relatively low dizygotic concordance (0.35).

25 hich indicated a high monozygotic and a zero dizygotic concordance for ADHD.

26 rs' ratings yielded moderate monozygotic and dizygotic concordance rates, in contrast to mothers' rep

27 documented monozygotic (MZ) and 380 same-sex dizygotic (DZ) pairs were ascertained from 1980 to 1992

28 female twins and 42 monozygotic (MZ) and 47 dizygotic (DZ) pairs.

29 Twenty-three monozygotic (MZ) and 20 dizygotic (DZ) proband pairs con- or discordant for schi

30 ncordant, compared with 4 of 15 B27-positive dizygotic (DZ) twin pairs (27%) and 4 of 32 DZ twin pair

31 of blood DNA from 52 monozygotic (MZ) and 27 dizygotic (DZ) twin pairs (aged 70-99 years).

32 was examined in 226 monozygotic (MZ) and 280 dizygotic (DZ) twin pairs aged 49 to 79 years (mean age,

33 Fewer than 5% of monozygotic (MZ) and dizygotic (DZ) twin pairs are clinically concordant for

34 cluding 10,527 monozygotic (MZ) and same-sex dizygotic (DZ) twin pairs discordant for education and s

35 The outcomes were assessed in up to 2,366 dizygotic (DZ) twin pairs from the Twins Early Developme

36 undus images from 43 monozygotic (MZ) and 32 dizygotic (DZ) twin pairs with AMD were examined.

37 Monozygotic (MZ) and dizygotic (DZ) twin pairs with and without ASD (aged 6-1

38 nited Kingdom (N = 1136 monozygotic (MZ) and dizygotic (DZ) twin pairs), genetic overlap was found be

39 healthy adult female monozygotic (MZ) and 28 dizygotic (DZ) twin pairs, analyzed bacterial 16S rRNA d

40 mtDNA genome sequences from 228 trios, eight dizygotic (DZ) twin quartets, and 10 monozygotic (MZ) tw

41 Spontaneous dizygotic (DZ) twinning occurs in 1%-4% of women, with f

42 y evidence that in some combatant countries, dizygotic (DZ) twinning rates (which also reportedly var

43 valuated in young adult monozygotic (MZ) and dizygotic (DZ) twins before and after the administration

44 t throughout cortex) in monozygotic (MZ) and dizygotic (DZ) twins discordant for chronic schizophreni

45 ed serum metabolites in monozygotic (MZ) and dizygotic (DZ) twins discordant for type 1 diabetes (T1D

46 pairs of monozygotic (MZ) twins, 57 pairs of dizygotic (DZ) twins, and 50 siblings].

47 twin design, including monozygotic (MZ) and dizygotic (DZ) twins, each twin was compared with their

48 ted number (n = 424) of monozygotic (MZ) and dizygotic (DZ) twins.

49 typed viral strains, in monozygotic (MZ) and dizygotic (DZ) twins.

50 art and reared-together monozygotic (MZ) and dizygotic (DZ) twins.

51 tive sib-pair linkage analysis in 119 female dizygotic (DZ) twins.

52 monozygotic (MZ) and nine pairs of same-sex dizygotic (DZ) twins.

53 values in same sex monozygotic (MZ) twins to dizygotic (DZ) twins.

54 e obtained from 483 monozygotic (MZ) and 472 dizygotic (DZ) unselected female twin pairs ages 21-81 y

55 t pairs of twins, 51 monozygotic (MZ) and 47 dizygotic (DZ), were recruited from the TwinsUK adult re

56 s of adult twins (64 monozygotic [MZ] and 53 dizygotic [DZ] pairs) were recruited.

57 selected women (181 monozygotic [MZ] and 351 dizygotic [DZ] twin pairs) recruited from a national reg

58 Twin Registry (261 monozygotic [MZ] and 524 dizygotic [DZ] twin pairs).

59 44 eyes, 45 pairs of monozygotic [MZ] and 41 dizygotic [DZ] twins).

60 ale twin pairs (707 monozygotic [MZ] and 491 dizygotic [DZ]) ascertained from a population-based regi

61 e-male twin pairs (818 monozygotic [MZ], 742 dizygotic [DZ]) of mean age (+/- SD) 74.2 +/- 2.8 yr.

62 gotic [MZ]) twin pairs and 511 nonidentical (dizygotic [DZ]) same-sex twin pairs (aged 20 to 80 years

63 for schizophrenia (6 monozygotic [MZ] and 1 dizygotic [DZ]), 52 pairs discordant for schizophrenia (

64 ozygotic [MZ]) and 71 same-sex nonidentical (dizygotic, [DZ]) twin pairs who were discordant for RA,

65 earning in a sample of monozygotic (MZA) and dizygotic (DZA) twins who had been reared apart.

66 activation profiles in 33 monozygotic and 22 dizygotic elderly twin pairs were studied.

67 cant but could be equated to the significant dizygotic estimate, suggesting a possible association wi

68 rt the results of a study of monozygotic and dizygotic female twins who were asked to decide either h

69 win-based heritability to estimates based on dizygotic identity-by-descent sharing and distant geneti

70 m era, 3360 pairs (1868 monozygotic and 1492 dizygotic) in which both members completed the pertinent

71 ixty-seven twin pairs, 30 monozygotic and 37 dizygotic, in which the proband had BPD were ascertained

72 hort 8-36 years of age (57% monozygotic, 40% dizygotic), including 372 subjects (46% with NDDs; 47% f

73 enty-three male twins (56 monozygotic and 67 dizygotic individuals; mean age 11.55 years; range, 10-1

74 postnatal life from eight pairs of mono- and dizygotic Malawian twins concordant for healthy growth a

75 a community sample of 194 monozygotic and 94 dizygotic male twins, ages 11-12 years.

76 rgy expenditure (PAEE) in 100 sex-concordant dizygotic (n = 38) and monozygotic (n = 62) twin pairs a

77 ncluding 3 sets of twins, 2 of which were of dizygotic origin.

78 ce interval [CI], 0.42-0.74) and 0.21 for 31 dizygotic pairs (95% CI, 0.09-0.43); for female twins, t

79 ic pairs (95% CI, 0.28-0.90) and 0.27 for 10 dizygotic pairs (95% CI, 0.09-0.69).

80 ic pairs (95% CI, 0.16-0.84) and 0.36 for 13 dizygotic pairs (95% CI, 0.11-0.60).

81 ic pairs (95% CI, 0.65-0.86) and 0.31 for 45 dizygotic pairs (95% CI, 0.16-0.46); for female twins, t

82 accounted for specifically by the discordant dizygotic pairs (P=.002).

83 ted for each syndrome in the monozygotic and dizygotic pairs and across the three pairings of schizop

84 re obtained from co-twins of monozygotic and dizygotic pairs discordant for schizophrenia and healthy

85 bined with those from 68 monozygotic and 109 dizygotic pairs in which the proband had UPD.

86 vailable data on 94 monozygotic pairs and 90 dizygotic pairs of elderly, White, male twins examined i

87 Of these, 38% of monozygotic and 26% of dizygotic pairs were diagnosed with the same cancer type

88 for 1216 twin pairs (384 monozygotic and 832 dizygotic pairs) after exclusions.

89 UK adult twin registry (112 monozygotic, 135 dizygotic pairs) age 21 to 81 years were studied.

90 y using twins (5477 monozygotic and same-sex dizygotic pairs) as "quasi-experimental" controls of gen

91 healthy older-aged twins (75 monozygotic/55 dizygotic pairs) enrolled in the Older Australian Twins

92 44 twin pairs (31 053 monozygotic and 47 991 dizygotic pairs), 52 independent samples, and 21 countri

93 tability estimates (50 monozygotic pairs, 34 dizygotic pairs), they nonetheless reveal high correlati

94 ins (both members of 546 monozygotic and 390 dizygotic pairs), who reported on the parenting they had

95 (n = 560, including 134 monozygotic and 142 dizygotic pairs).

96 dant for type 1 diabetes (32 monozygotic, 32 dizygotic pairs).

97 diabetic female twins, 39 monozygotic and 45 dizygotic pairs, aged 21-74 years.

98 event was 5.64 in all subjects, 4.52 within dizygotic pairs, and 3.58 within monozygotic pairs.

99 members of 485 monozygotic pairs and of 335 dizygotic pairs, were interviewed by telephone to assess

100 of women from monozygotic pairs or same-sex dizygotic pairs.

101 was somewhat stronger in monozygotic than in dizygotic pairs.

102 ic twin pairs and 0.47 (95% CI 0.39-0.55) in dizygotic pairs.

103 d at 0.67 for monozygotic pairs and 0.44 for dizygotic pairs.

104 pairs was significantly greater than that in dizygotic pairs.

105 Registry, including 119 monozygotic and 301 dizygotic pairs.

106 uded both members of 486 monozygotic and 335 dizygotic pairs.

107 MD in cotwins-greater in monozygotic than in dizygotic pairs.

108 semblance was greater in monozygotic than in dizygotic pairs.

109 emale twins, including 27 monozygotic and 47 dizygotic pairs.

110 females), 120 monozygotic and 76 same-gender dizygotic pairs.

111 2]) remained among monozygotic pairs but not dizygotic pairs.

112 s carriage among 617 twin pairs (monozygotic/dizygotic pairs: 112/505) was 26.3% (95% confidence inte

113 gher in monozygotic (r = 0.71) compared with dizygotic (r = 0.50) twin pairs, suggesting a substantia

114 interval, 1.09-1.55; P=0.003), compared with dizygotic same sex (hazard ratio, 1.16; 95% confidence i

115 in Cohort included 2482 monozygotic and 5113 dizygotic same-sex male and female twin pairs born betwe

116 es were completed by 385 monozygotic and 486 dizygotic same-sex twin families (37% male twin pair fam

117 d in 1654 twins from 420 monozygotic and 352 dizygotic same-sex twin pairs aged 56.3 +/- 10.4 y with

118 imilarity was not significantly greater than dizygotic similarity.

119 ic local electric field was designed by IrRu dizygotic single-atom sites (IrRu DSACs) to tune the H(2

120 in age at onset was significantly greater in dizygotic than in monozygotic pairs, suggesting genetic

121 The higher risks of these cancers in dizygotic than in monozygotic twins support a prenatal a

122 them genetically in between monozygotic and dizygotic; they are sesquizygotic.

123 ys and 86 adult twins (52 monozygotic and 34 dizygotic) to understand how heritability factors influe

124 Increased monozygotic versus dizygotic twin concordance rates indicate that heredity,

125 ygotic twins (0.70) was more than double the dizygotic twin correlation (0.29), evidence for a high g

126 The primary outcomes were monozygotic and dizygotic twin correlations.

127 d by intrauterine growth restriction or from dizygotic twin gestation where one twin exhibited growth

128 y of 80,309 monozygotic and 123,382 same-sex dizygotic twin individuals (N = 203,691) within the popu

129 ery is elevated in monozygotic compared with dizygotic twin mothers but not in monozygotic twin fathe

130 ion was higher in monozygotic (0.72) than in dizygotic twin pairs (0.30), indicating a strong genetic

131 ficantly higher in 18 monozygotic than in 16 dizygotic twin pairs (55% vs 18%, respectively).

132 current sample contains 2324 monozygotic and dizygotic twin pairs (mean [SD] age 29.9 [2.5] years) fo

133 With a sample of 312 monozygotic- and 298 dizygotic twin pairs (N = 1220), we measured people's pr

134 dds ratio [OR], 2.28; 95% CI, 2.19-2.37) and dizygotic twin pairs (within-pairs OR, 1.65; 95% CI, 1.3

135 iated with all 7 outcomes within sibling and dizygotic twin pairs and 3 outcomes within monozygotic t

136 0% female, including 170 monozygotic and 219 dizygotic twin pairs and 337 unrelated individuals), we

137 cluding 396 boys from 102 monozygotic and 96 dizygotic twin pairs and 396 girls from 112 monozygotic

138 and concordance rates for monozygotic versus dizygotic twin pairs as measures of relative risk (RR).

139 None of the dizygotic twin pairs became clinically concordant.

140 Monozygotic and dizygotic twin pairs completed a belief formation task.

141 communities of adult female monozygotic and dizygotic twin pairs concordant for leanness or obesity,

142 The analysis of DNMs in 111 dizygotic twin pairs did not identify a substantial fami

143 e 75% in the 12 monozygotic and 22% in the 9 dizygotic twin pairs evaluated twice.

144 least 12 months apart in 1,057 opposite-sex dizygotic twin pairs from a population-based register.

145 ins Early Development Study (TEDS) and 6,040 dizygotic twin pairs from the Child and Adolescent Twin

146 Subjects included 3,842 dizygotic twin pairs from the Twins Early Development St

147 Seventy-seven monozygotic and 89 same-sex dizygotic twin pairs in which the proband met the Resear

148 Within dizygotic twin pairs only, associations between growth a

149 Adult monozygotic and dizygotic twin pairs recruited from the TwinsUK cohort.

150 89 monozygotic and 196 dizygotic twin pairs were analysed for factor VII.

151 observed no evidence of sesquizygosis in 968 dizygotic twin pairs whom we screened by means of pangen

152 Eighty twin subjects (20 monozygotic and 20 dizygotic twin pairs) viewed a moving sinusoidal grating

153 otal of 86 twin pairs (32 monozygotic and 54 dizygotic twin pairs) were included in this study.

154 in 4602 subjects (1152 monozygotic and 1149 dizygotic twin pairs), aged between 16 and 82 years, rec

155 participants in total (59 monozygotic and 46 dizygotic twin pairs).

156 community-dwelling twins (45 monozygotic, 20 dizygotic twin pairs, 130 total subjects) from southern

157 cipants were 345 monozygotic twin pairs, 337 dizygotic twin pairs, 306 biological sibling pairs, and

158 phrenia (DS), healthy MZ twin pairs, healthy dizygotic twin pairs, and healthy nonrelated subject pai

159 articipants, including 27 monozygotic and 18 dizygotic twin pairs, were sampled mainly at ages 12-13,

160 g the correlation in 100 monozygotic and 100 dizygotic twin pairs.

161 f co-variation between adult monozygotic and dizygotic twin pairs.

162 Results were similar in monozygotic and dizygotic twin pairs.

163 aged 18-80 years, comprising 1,025 complete dizygotic twin pairs.

164 ng correlation among 160 monozygotic and 349 dizygotic twin pairs.

165 ory were examined in 222 monozygotic and 184 dizygotic twin pairs.

166 pitch, to 136 monozygotic twin pairs and 148 dizygotic twin pairs.

167 148 women comprising 160 monozygotic and 414 dizygotic twin pairs.

168 ronment assumption regarding monozygotic and dizygotic twin pairs.

169 substantially greater in monozygotic than in dizygotic twin pairs.

170 amined in a group of 179 monozygotic and 158 dizygotic twin pairs.

171 r but still substantial correlations between dizygotic twin pairs.

172 airs are statistically not more similar than dizygotic twin pairs.

173 rs and 396 girls from 112 monozygotic and 86 dizygotic twin pairs; Children's 24-h dietary intake was

174 We find that within families, the dizygotic twin with the higher PGS is more likely to att

175 We find that within families, the dizygotic twin with the higher PGS is more likely to att

176 ption frequency by comparing monozygotic and dizygotic twin-pair groups with structural equation anal

177 These included 115 monozygotic and 183 dizygotic twin-pairs.

178 S, we resolve the FSHB locus in the GWAS for dizygotic twinning and further leverage this framework t

179 nning are not competing strategies; instead, dizygotic twinning is the outcome of an adaptive conditi

180 Dizygotic twinning probably involves high hormone concen

181 ning female fertility accords with a falling dizygotic twinning rate during the same period.

182 Dizygotic twinning, the simultaneous birth of siblings w

183 ptional intermediate between monozygotic and dizygotic twinning.

184 ate for monozygotic twins was double that of dizygotic twins (0.16 [95% CI, 0.11-0.22] vs 0.07 [95% C

185 ings (population cohort) and monozygotic and dizygotic twins (CATSS cohort) provided estimates of the

186 concordant and 52 from discordant pairs) and dizygotic twins (n = 274, with 39 patients from discorda

187 Monozygotic twins (n = 1), dizygotic twins (n = 3) and triplets (n = 1) were includ

188 Among the dizygotic twins (n = 8), no set was found to be concorda

189 monozygotic twins (N=98 pairs) and 0.37 for dizygotic twins (N=134 pairs).

190 .43; 95% CI, 0.50-4.07; P = .50) relative to dizygotic twins (OR, 2.13; 95% CI, 1.03-4.39; P = .04).

191 zygotic twins was 0.04 compared with 0.49 in dizygotic twins (P = .005).

192 were 0.04 for monozygotic twins and 0.37 for dizygotic twins (P = .01).

193 monozygotic twins (r = 0.88), but not across dizygotic twins (r = 0.32) or unrelated subjects (r = 0.

194 wins (r(2) = 0.48; P < .002) but not between dizygotic twins (r(2) = 0.12; P = .7).

195 ins (r(2) = 0.70; P < .0001) but not between dizygotic twins (r(2) = 0.36; P = .2).

196 99) were significantly higher than those for dizygotic twins (range, 0.22-0.65), giving heritability

197 s for ADHD were greater for monozygotic than dizygotic twins according to both mothers' and teachers'

198 he increased concordance of monozygotic over dizygotic twins and adoption studies showing increased r

199 Using dizygotic twins and Markov analyses of their vocal seque

200 Results were equivalent to those in dizygotic twins and persisted when controlling for prior

201 tic twins, all dizygotic twins, the same-sex dizygotic twins and sibling pairs, and all dizygotic twi

202 x dizygotic twins and sibling pairs, and all dizygotic twins and sibling pairs.

203 opment by replicating anatomical findings in dizygotic twins and unrelated singletons.

204 nal dynamics were significantly different in dizygotic twins but not in monozygotic twins.

205 sed risks of breast and testicular cancer in dizygotic twins compared with monozygotic twins, and in

206 Male monozygotic and dizygotic twins concordant or discordant for AD and cont

207 Here we study monozygotic and dizygotic twins discordant for ASD to test whether fetal

208 Monozygotic and dizygotic twins discordant for mental disorders were scr

209 sample comprised phenotyped monozygotic and dizygotic twins enriched for NDCs.

210 ipose and blood samples from monozygotic and dizygotic twins for the characterization of non-genetic

211 wins were significantly more similar than in dizygotic twins for the face and place stimuli, but ther

212 in monozygotic twins; b = 0.79, P = 0.01 in dizygotic twins from 0 to 1 mo) were identified.

213 in monozygotic twins; b = -1.64, P = 0.82 in dizygotic twins from 12 to 24 mo) were found.

214 Dizygotic twins had discordant variants in TYR, OCA2 and

215 sion in 1,404 complete pairs of opposite-sex dizygotic twins identified through a population-based re

216 iance-covariance matrices of monozygotic and dizygotic twins indicated that 48% of the observed varia

217 The concordance rate of PD in pairs of dizygotic twins is similar to that in pairs of monozygot

218 have established that disease concordance in dizygotic twins is the same as that in siblings generall

219 ns matched to 72 control participants and 40 dizygotic twins matched to 58 control participants.

220 high hormone concentrations, and therefore, dizygotic twins might be at raised risk of these cancers

221 th monozygotic twins, and in monozygotic and dizygotic twins of probands.

222 greater in the monozygotic twins than in the dizygotic twins or in the dizygotic twins plus nontwin s

223 twins than in the dizygotic twins or in the dizygotic twins plus nontwin siblings.

224 Participants were monozygotic and dizygotic twins randomly recruited from the Vietnam Era

225 ences in the risk factors in monozygotic and dizygotic twins separately.

226 esticular cancer was significantly higher in dizygotic twins than in monozygotic twins (1.5 [1.1-2.2]

227 issues conducted in a large set of mono- and dizygotic twins that allows systematic dissection of gen

228 ample as well as in pairs of monozygotic and dizygotic twins that were discordant for each measure of

229 ye-tracking data obtained in monozygotic and dizygotic twins to assess their heritability and their i

230 mparing concordance rates in monozygotic and dizygotic twins to concordance between mothers and their

231 casewise concordance between monozygotic and dizygotic twins was found for any specific gene, subgrou

232 By comparing BIPR between monozygotic and dizygotic twins we show that BIPR have a heritable compo

233 lues (ABI< or =0.9) for both monozygotic and dizygotic twins were significantly greater than would be

234 ional study was conducted of monozygotic and dizygotic twins who were reared apart or reared together

235 Offspring of monozygotic and dizygotic twins with a history of AD were significantly

236 S (15.2%) was greater than the proportion of dizygotic twins with IBS who have co-twins with IBS (6.7

237 However, the proportion of dizygotic twins with IBS who have mothers with IBS (15.2

238 or 324 of the twins (151 monozygotic and 173 dizygotic twins).

239 yte mtDNA samples from 20 monozygotic and 18 dizygotic twins, 60-75 years old, 30% (P = 0.0007) and 2

240 6274 for exposed vs 27 for unexposed ); for dizygotic twins, 8.2 (95% CI, 3.7-18.1; rate, 805 for ex

241 otic twins to the similarity in the same-sex dizygotic twins, all dizygotic twins, the same-sex dizyg

242 n 458 pairs of monozygotic and 1099 pairs of dizygotic twins, all women with a mean age of 46 y was p

243 ity between monozygotic twins, 5.14% between dizygotic twins, and 4.51% between none-twin siblings, r

244 n infant sample including 58 singletons, 132 dizygotic twins, and 98 monozygotic twins with rsfMRI sc

245 ur among human cohorts with a propensity for dizygotic twins, and polymorphisms in GDF9 and BMP15 are

246 defect among monozygotic twins compared with dizygotic twins, and the congenital heart defect occurre

247 d twin gestations or between monozygotic and dizygotic twins, but heritability analysis showed herita

248 Comparison of monozygotic and dizygotic twins, differentiating genetic similarities of

249 and mean distribution of lengths may vary in dizygotic twins, indicating individual rates of developm

250 Regarding the comparison between mono- and dizygotic twins, more significant percentage of monozygo

251 -degree relatives, including monozygotic and dizygotic twins, mothers, fathers, full siblings, matern

252 of lens area) was similar in monozygotic and dizygotic twins, occurring in 19.4% and 20.6% with the c

253 ived and executed studies of monozygotic and dizygotic twins, one in Sweden and one in the United Sta

254 ich was greater among monozygotic than among dizygotic twins, predicted the twins' resemblance in can

255 eruption was 21% and 18% in monozygotic and dizygotic twins, respectively.

256 orrelations were higher for monozygotic than dizygotic twins, suggesting important genetic influences

257 t doubled in monozygotic twins compared with dizygotic twins, suggesting the influence of genetic fac

258 ilarity in the same-sex dizygotic twins, all dizygotic twins, the same-sex dizygotic twins and siblin

259 iate genetic models based on monozygotic and dizygotic twins, we discovered that partially overlappin

260 ltiple embryos, 2) raising the proportion of dizygotic twins, which leads to a higher occurrence of o

261 eart defect occurrence was also increased in dizygotic twins, who are all dichorionic.

262 amined 268 asymptomatic male monozygotic and dizygotic twins.

263 tistically significant, was also found among dizygotic twins.

264 gut microbiomes of lean and obese mono- and dizygotic twins.

265 airs of monozygotic and 86 pairs of same-sex dizygotic twins.

266 s; 149 pairs of monozygotic and 352 pairs of dizygotic twins.

267 right and left eyes and for monozygotic and dizygotic twins.

268 relation were calculated for monozygotic and dizygotic twins.

269 h more in terms of class membership than did dizygotic twins.

270 consistently greater in monozygotic than in dizygotic twins.

271 illness more strongly in monozygotic than in dizygotic twins.

272 twins and 14.6% and 32.8%, respectively, in dizygotic twins.

273 etween 65-70%, compared to between 15-20% in dizygotic twins.

274 concordance rate in monozygotic compared to dizygotic twins.

275 of SZ is 33% in monozygotic twins and 7% in dizygotic twins.

276 lative risks were higher in monozygotic than dizygotic twins.

277 wins compared with 5.5 (95% CI, 3.3-8.6) for dizygotic twins.

278 nd opposite sex (21.4%; 95% CI, 12.0%-33.4%) dizygotic twins.

279 US metropolitan areas and included mono- and dizygotic twins.

280 tophaga in monozygotic twins and Kingella in dizygotic twins.

281 in concordance rates between monozygotic and dizygotic twins.

282 826 were identified as monozygotic twins and dizygotic twins/siblings, respectively.

283 an international registry of monozygotic and dizygotic twins/triplets (n = 63 EoE "Twins" probands).

284 blings: n = 513; monozygotic twins: n = 207; dizygotic twins: n = 189), the authors examined longitud

285 nozygotic twins; 7.4 (95% CI = 1.0-55.3) for dizygotic twins; 4.7 (95% CI = 3.9-5.6) for full sibling

286 cystic kidneys in utero, in one of a pair of dizygotic twins; the other twin has the mutation but no

287 nhibitor by ELISA in 118 monozygotic and 112 dizygotic unselected female twins aged 21-73 years from

288 33 same-sex twin pairs; 51% monozygotic, 49% dizygotic), we demonstrate that genetic factors do indee

289 he adult twin pairs (145 monozygotic and 117 dizygotic) who both had children, who reported on the pa

290 irs of female twins (226 monozygotic and 280 dizygotic) who were 50 to 79 years old (mean, 62).

291 ale twin volunteers (226 monozygotic and 280 dizygotic) with a mean age of 62 years (range, 49-79 yea

292 l of 224 twin probands (106 monozygotic, 118 dizygotic) with a same-sex co-twin and a lifetime histor

293 15 years: 67 twin pairs (34 monozygotic; 33 dizygotic) with concordance or discordance for ADHD symp

294 Monozygotic and dizygotic within-pair serum 25(OH)D correlations were si

295 393 twins: 230 were monozygotic and 159 were dizygotic (zygosity was unknown for 4).