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1 or 324 of the twins (151 monozygotic and 173 dizygotic twins).
2 relation were calculated for monozygotic and dizygotic twins.
3 right and left eyes and for monozygotic and dizygotic twins.
4 h more in terms of class membership than did dizygotic twins.
5 consistently greater in monozygotic than in dizygotic twins.
6 illness more strongly in monozygotic than in dizygotic twins.
7 twins and 14.6% and 32.8%, respectively, in dizygotic twins.
8 etween 65-70%, compared to between 15-20% in dizygotic twins.
9 concordance rate in monozygotic compared to dizygotic twins.
10 of SZ is 33% in monozygotic twins and 7% in dizygotic twins.
11 lative risks were higher in monozygotic than dizygotic twins.
12 tophaga in monozygotic twins and Kingella in dizygotic twins.
13 wins compared with 5.5 (95% CI, 3.3-8.6) for dizygotic twins.
14 nd opposite sex (21.4%; 95% CI, 12.0%-33.4%) dizygotic twins.
15 US metropolitan areas and included mono- and dizygotic twins.
16 in concordance rates between monozygotic and dizygotic twins.
17 amined 268 asymptomatic male monozygotic and dizygotic twins.
18 tistically significant, was also found among dizygotic twins.
19 gut microbiomes of lean and obese mono- and dizygotic twins.
20 airs of monozygotic and 86 pairs of same-sex dizygotic twins.
21 s; 149 pairs of monozygotic and 352 pairs of dizygotic twins.
22 ptional intermediate between monozygotic and dizygotic twinning.
23 ate for monozygotic twins was double that of dizygotic twins (0.16 [95% CI, 0.11-0.22] vs 0.07 [95% C
24 nozygotic twins; 7.4 (95% CI = 1.0-55.3) for dizygotic twins; 4.7 (95% CI = 3.9-5.6) for full sibling
25 yte mtDNA samples from 20 monozygotic and 18 dizygotic twins, 60-75 years old, 30% (P = 0.0007) and 2
26 6274 for exposed vs 27 for unexposed ); for dizygotic twins, 8.2 (95% CI, 3.7-18.1; rate, 805 for ex
27 s for ADHD were greater for monozygotic than dizygotic twins according to both mothers' and teachers'
28 otic twins to the similarity in the same-sex dizygotic twins, all dizygotic twins, the same-sex dizyg
29 n 458 pairs of monozygotic and 1099 pairs of dizygotic twins, all women with a mean age of 46 y was p
30 S, we resolve the FSHB locus in the GWAS for dizygotic twinning and further leverage this framework t
31 he increased concordance of monozygotic over dizygotic twins and adoption studies showing increased r
34 tic twins, all dizygotic twins, the same-sex dizygotic twins and sibling pairs, and all dizygotic twi
37 ity between monozygotic twins, 5.14% between dizygotic twins, and 4.51% between none-twin siblings, r
38 n infant sample including 58 singletons, 132 dizygotic twins, and 98 monozygotic twins with rsfMRI sc
39 ur among human cohorts with a propensity for dizygotic twins, and polymorphisms in GDF9 and BMP15 are
40 defect among monozygotic twins compared with dizygotic twins, and the congenital heart defect occurre
42 d twin gestations or between monozygotic and dizygotic twins, but heritability analysis showed herita
43 ings (population cohort) and monozygotic and dizygotic twins (CATSS cohort) provided estimates of the
44 sed risks of breast and testicular cancer in dizygotic twins compared with monozygotic twins, and in
47 ygotic twins (0.70) was more than double the dizygotic twin correlation (0.29), evidence for a high g
53 ipose and blood samples from monozygotic and dizygotic twins for the characterization of non-genetic
54 wins were significantly more similar than in dizygotic twins for the face and place stimuli, but ther
57 d by intrauterine growth restriction or from dizygotic twin gestation where one twin exhibited growth
59 sion in 1,404 complete pairs of opposite-sex dizygotic twins identified through a population-based re
60 iance-covariance matrices of monozygotic and dizygotic twins indicated that 48% of the observed varia
61 and mean distribution of lengths may vary in dizygotic twins, indicating individual rates of developm
62 y of 80,309 monozygotic and 123,382 same-sex dizygotic twin individuals (N = 203,691) within the popu
63 nning are not competing strategies; instead, dizygotic twinning is the outcome of an adaptive conditi
65 have established that disease concordance in dizygotic twins is the same as that in siblings generall
67 high hormone concentrations, and therefore, dizygotic twins might be at raised risk of these cancers
68 Regarding the comparison between mono- and dizygotic twins, more significant percentage of monozygo
69 ery is elevated in monozygotic compared with dizygotic twin mothers but not in monozygotic twin fathe
70 -degree relatives, including monozygotic and dizygotic twins, mothers, fathers, full siblings, matern
71 concordant and 52 from discordant pairs) and dizygotic twins (n = 274, with 39 patients from discorda
75 blings: n = 513; monozygotic twins: n = 207; dizygotic twins: n = 189), the authors examined longitud
76 of lens area) was similar in monozygotic and dizygotic twins, occurring in 19.4% and 20.6% with the c
78 ived and executed studies of monozygotic and dizygotic twins, one in Sweden and one in the United Sta
79 greater in the monozygotic twins than in the dizygotic twins or in the dizygotic twins plus nontwin s
80 .43; 95% CI, 0.50-4.07; P = .50) relative to dizygotic twins (OR, 2.13; 95% CI, 1.03-4.39; P = .04).
83 ption frequency by comparing monozygotic and dizygotic twin-pair groups with structural equation anal
84 ion was higher in monozygotic (0.72) than in dizygotic twin pairs (0.30), indicating a strong genetic
86 current sample contains 2324 monozygotic and dizygotic twin pairs (mean [SD] age 29.9 [2.5] years) fo
87 With a sample of 312 monozygotic- and 298 dizygotic twin pairs (N = 1220), we measured people's pr
88 dds ratio [OR], 2.28; 95% CI, 2.19-2.37) and dizygotic twin pairs (within-pairs OR, 1.65; 95% CI, 1.3
89 iated with all 7 outcomes within sibling and dizygotic twin pairs and 3 outcomes within monozygotic t
90 0% female, including 170 monozygotic and 219 dizygotic twin pairs and 337 unrelated individuals), we
91 cluding 396 boys from 102 monozygotic and 96 dizygotic twin pairs and 396 girls from 112 monozygotic
92 and concordance rates for monozygotic versus dizygotic twin pairs as measures of relative risk (RR).
95 communities of adult female monozygotic and dizygotic twin pairs concordant for leanness or obesity,
98 least 12 months apart in 1,057 opposite-sex dizygotic twin pairs from a population-based register.
99 ins Early Development Study (TEDS) and 6,040 dizygotic twin pairs from the Child and Adolescent Twin
101 Seventy-seven monozygotic and 89 same-sex dizygotic twin pairs in which the proband met the Resear
105 observed no evidence of sesquizygosis in 968 dizygotic twin pairs whom we screened by means of pangen
106 Eighty twin subjects (20 monozygotic and 20 dizygotic twin pairs) viewed a moving sinusoidal grating
108 in 4602 subjects (1152 monozygotic and 1149 dizygotic twin pairs), aged between 16 and 82 years, rec
110 community-dwelling twins (45 monozygotic, 20 dizygotic twin pairs, 130 total subjects) from southern
111 cipants were 345 monozygotic twin pairs, 337 dizygotic twin pairs, 306 biological sibling pairs, and
112 phrenia (DS), healthy MZ twin pairs, healthy dizygotic twin pairs, and healthy nonrelated subject pai
113 articipants, including 27 monozygotic and 18 dizygotic twin pairs, were sampled mainly at ages 12-13,
127 rs and 396 girls from 112 monozygotic and 86 dizygotic twin pairs; Children's 24-h dietary intake was
130 ich was greater among monozygotic than among dizygotic twins, predicted the twins' resemblance in can
132 monozygotic twins (r = 0.88), but not across dizygotic twins (r = 0.32) or unrelated subjects (r = 0.
136 99) were significantly higher than those for dizygotic twins (range, 0.22-0.65), giving heritability
141 orrelations were higher for monozygotic than dizygotic twins, suggesting important genetic influences
142 t doubled in monozygotic twins compared with dizygotic twins, suggesting the influence of genetic fac
143 esticular cancer was significantly higher in dizygotic twins than in monozygotic twins (1.5 [1.1-2.2]
144 issues conducted in a large set of mono- and dizygotic twins that allows systematic dissection of gen
145 ample as well as in pairs of monozygotic and dizygotic twins that were discordant for each measure of
147 ilarity in the same-sex dizygotic twins, all dizygotic twins, the same-sex dizygotic twins and siblin
148 cystic kidneys in utero, in one of a pair of dizygotic twins; the other twin has the mutation but no
149 ye-tracking data obtained in monozygotic and dizygotic twins to assess their heritability and their i
150 mparing concordance rates in monozygotic and dizygotic twins to concordance between mothers and their
151 an international registry of monozygotic and dizygotic twins/triplets (n = 63 EoE "Twins" probands).
152 casewise concordance between monozygotic and dizygotic twins was found for any specific gene, subgrou
153 By comparing BIPR between monozygotic and dizygotic twins we show that BIPR have a heritable compo
154 iate genetic models based on monozygotic and dizygotic twins, we discovered that partially overlappin
155 lues (ABI< or =0.9) for both monozygotic and dizygotic twins were significantly greater than would be
156 ltiple embryos, 2) raising the proportion of dizygotic twins, which leads to a higher occurrence of o
157 ional study was conducted of monozygotic and dizygotic twins who were reared apart or reared together
162 S (15.2%) was greater than the proportion of dizygotic twins with IBS who have co-twins with IBS (6.7