X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
female (809) 809
humans (805) 805
pregnancy (728) 728
index medicus (563) 563
obstetrics & gynecology (457) 457
adult (452) 452
pregnancy-associated plasma protein-a - metabolism (349) 349
pregnancy-associated plasma protein-a - analysis (337) 337
papp-a (320) 320
chorionic gonadotropin, beta subunit, human - blood (314) 314
genetics & heredity (266) 266
biomarkers - blood (254) 254
pregnancy trimester, first (248) 248
down syndrome - diagnosis (229) 229
human chorionic-gonadotropin (206) 206
nuchal translucency (186) 186
animals (174) 174
prenatal diagnosis - methods (163) 163
gestational age (158) 158
nuchal translucency measurement (157) 157
free beta-hcg (156) 156
pregnancy-associated plasma protein-a - genetics (156) 156
maternal age (150) 150
pregnancy trimester, first - blood (144) 144
plasma-protein-a (143) 143
risk (139) 139
male (135) 135
prenatal diagnosis (135) 135
down syndrome (126) 126
pregnant women (122) 122
1st trimester (118) 118
pregnancy-associated plasma protein-a (118) 118
case-control studies (117) 117
middle aged (117) 117
trisomy-21 (117) 117
papp‐a (111) 111
ultrasonography, prenatal (109) 109
down syndrome - blood (107) 107
risk factors (101) 101
expression (98) 98
young adult (96) 96
false positive reactions (95) 95
down-syndrome (91) 91
retrospective studies (91) 91
aneuploidy (90) 90
predictive value of tests (89) 89
prospective studies (89) 89
preeclampsia (85) 85
adolescent (84) 84
analysis (84) 84
1st-trimester (82) 82
proteins (81) 81
gestation (80) 80
prenatal screening (78) 78
reproductive biology (78) 78
blood proteins (76) 76
mice (76) 76
plasma protein-a (75) 75
endocrinology & metabolism (74) 74
sensitivity and specificity (73) 73
placenta (72) 72
trisomy 21 (71) 71
free β-hcg (70) 70
infant, newborn (70) 70
fetuses (67) 67
research (67) 67
ultrasound (67) 67
age (66) 66
chorionic gonadotropin (66) 66
fetal nuchal translucency (65) 65
first trimester (64) 64
down syndrome - diagnostic imaging (63) 63
trisomy - diagnosis (63) 63
downs-syndrome (62) 62
pregnancy-associated plasma protein a (60) 60
free β‐hcg (59) 59
major basic-protein (59) 59
women (59) 59
biomarkers (58) 58
obstetrics and gynecology (57) 57
screening (57) 57
first-trimester screening (56) 56
acoustics (53) 53
radiology, nuclear medicine & medical imaging (53) 53
cell biology (52) 52
chorionic gonadotropin - blood (52) 52
diagnosis (52) 52
gene expression (52) 52
neck - diagnostic imaging (52) 52
cohort studies (51) 51
research article (50) 50
trisomy (50) 50
ultrasonography (50) 50
protein binding (48) 48
risk assessment (48) 48
insulin (47) 47
insulin-like growth factor binding protein 4 - metabolism (47) 47
physiological aspects (47) 47
pre-eclampsia - blood (47) 47
intrauterine growth restriction (46) 46
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (939) 939
German (9) 9
French (6) 6
Chinese (5) 5
Russian (4) 4
Bulgarian (1) 1
Czech (1) 1
Japanese (1) 1
Polish (1) 1
Spanish (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Marouli, Eirini and Graff, Mariaelisa and Medina-Gomez, Carolina and Lo, Ken Sin and Wood, Anew R and Kjaer, Troels R and Fine, Rebecca S and Lu, Yingchang and Schurmann, Claudia and Highland, Heather M and Rüeger, Sina and Thorleifsson, Gudmar and Justice, Anne E and Lamparter, David and Stirrups, Kathleen E and Turcot, Valérie and Young, Kristin L and Winkler, Thomas W and Esko, Tõnu and Karaderi, Tugce and Locke, Adam E and Masca, Nicholas G. D and Ng, Maggie C. Y and Mudgal, Poorva and Rivas, Manuel A and Vedantam, Sailaja and Mahajan, Anubha and Guo, Xiuqing and Abecasis, Goncalo and Aben, Katja K and Adair, Linda S and Alam, Dewan S and Albrecht, Eva and Allin, Kristine H and Allison, Matthew and Amouyel, Philippe and Appel, Emil V and Arveiler, Dominique and Asselbergs, Folkert W and Auer, Paul L and Balkau, Beverley and Banas, Bernhard and Bang, Lia E and Benn, Marianne and Bergmann, Sven and Bielak, Lawrence F and Blüher, Matthias and Boeing, Heiner and Boerwinkle, Eric and Böger, Carsten A and Bonnycastle, Lori L and Bork-Jensen, Jette and Bots, Michiel L and Bottinger, Erwin P and Bowden, Donald W and Brandslund, Ivan and Breen, Gerome and Brilliant, Murray H and Broer, Linda and Burt, Amber A and Butterworth, Adam S and Carey, David J and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Yii-Der Ida and Chowdhury, Rajiv and Christensen, Cramer and Chu, Auey Y and Cocca, Massimiliano and Collins, Francis S and Cook, James P and Corley, Janie and Galbany, Jordi Corominas and Cox, Amanda J and Cuellar-Partida, Gabriel and Danesh, John and Davies, Gail and de Bakker, Paul I. W and de Borst, Gert J and de Denus, Simon and de Groot, Mark C. H and de Mutsert, Renée and Deary, Ian J and Dedoussis, George and Demerath, Ellen W and den Hollander, Anneke I and Dennis, Joe G and Di Angelantonio, Emanuele and nos, Fotios and Du, Mengmeng and Dunning, Alison M and Easton, Douglas F and Ebeling, Tapani and Edwards, Todd L and Ellinor, Patrick T and Elliott, Paul and Evangelou, Evangelos and Farmaki, Aliki-Eleni and Faul, Jessica D and ... and EPIC-CVD Consortium and GoT2D Genes Consortium and MAGIC Investigators and Global Lipids Genetics Consortium and EPIC-InterAct Consortium and ReproGen Consortium and ExomeBP Consortium and CHD Exome Consortium and T2D-Genes Consortium and The EPIC-InterAct Consortium and CHD Exome+ Consortium and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Geriatrik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
Nature, ISSN 0028-0836, 2017, Volume 542, Issue 7640, pp. 186 - 190
Height is a highly heritable, classic polygenic trait with approximately 700 common associated variants identified through genome-wide association studies so... 
MISSING HERITABILITY | GENETIC ARCHITECTURE | INTERLEUKIN-11 | MUTATIONS | MULTIDISCIPLINARY SCIENCES | GENOME-WIDE ASSOCIATION | Stature | Genetic aspects | Observations | Genetic variation | Studies | Datasets | Disease | Genes | Deoxyribonucleic acid--DNA | Genetik | Biological Sciences | Genetics | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
Journal Article
EMBO Molecular Medicine, ISSN 1757-4676, 04/2016, Volume 8, Issue 4, pp. 363 - 374
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 09/2015, Volume 290, Issue 36, pp. 21915 - 21924
Journal Article
Development, ISSN 0950-1991, 03/2004, Volume 131, Issue 5, pp. 1187 - 1194
Journal Article
Journal Article
Journal Article
Journal Article
Trends in Endocrinology & Metabolism, ISSN 1043-2760, 2012, Volume 23, Issue 5, pp. 242 - 249
Journal Article
American Journal of Physiology - Heart and Circulatory Physiology, ISSN 0363-6135, 08/2010, Volume 299, Issue 2, pp. 284 - 291
Journal Article
Journal Article
Cardiovascular Research, ISSN 0008-6363, 06/2018, Volume 114, Issue 7, pp. 992 - 1005
Journal Article
Journal Article
14.