ライフサイエンスコーパス: dizygotic twin

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

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

3 consistently greater in monozygotic than in dizygotic twins.

4 illness more strongly in monozygotic than in dizygotic twins.

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

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

7 concordance rate in monozygotic compared to dizygotic twins.

8 relation were calculated for monozygotic and dizygotic twins.

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

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

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

12 in concordance rates between monozygotic and dizygotic twins.

13 amined 268 asymptomatic male monozygotic and dizygotic twins.

14 tistically significant, was also found among dizygotic twins.

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

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

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

18 lative risks were higher in monozygotic than dizygotic twins.

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

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

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

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

23 6274 for exposed vs 27 for unexposed ); for dizygotic twins, 8.2 (95% CI, 3.7-18.1; rate, 805 for ex

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

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

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

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

28 Using dizygotic twins and Markov analyses of their vocal seque

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

65 .43; 95% CI, 0.50-4.07; P = .50) relative to dizygotic twins (OR, 2.13; 95% CI, 1.03-4.39; P = .04).

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

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

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

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

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

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

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

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

74 None of the dizygotic twin pairs became clinically concordant.

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

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

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

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

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

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

81 Within dizygotic twin pairs only, associations between growth a

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

83 89 monozygotic and 196 dizygotic twin pairs were analysed for factor VII.

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

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

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

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

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

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

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

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

92 ronment assumption regarding monozygotic and dizygotic twin pairs.

93 substantially greater in monozygotic than in dizygotic twin pairs.

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

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

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

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

98 Results were similar in monozygotic and dizygotic twin pairs.

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

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

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

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

103 148 women comprising 160 monozygotic and 414 dizygotic twin pairs.

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

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

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

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

108 Dizygotic twinning probably involves high hormone concen

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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