Search Filters
Format Format
Subjects Subjects
Subjects Subjects
Sort by Item Count (A-Z)
Filter by Count
humans (220) 220
index medicus (216) 216
genetics & heredity (119) 119
female (116) 116
male (112) 112
mutation (70) 70
phenotype (59) 59
genomic imprinting (54) 54
adult (53) 53
silver-russell syndrome (53) 53
dna methylation (50) 50
syndrome (44) 44
genetic aspects (40) 40
methylation (39) 39
uniparental disomy (39) 39
child (36) 36
biochemistry & molecular biology (35) 35
infant (35) 35
silver-russell syndrome - genetics (34) 34
abnormalities, multiple - genetics (33) 33
pediatrics (33) 33
genotype (32) 32
growth disorders - genetics (31) 31
mutations (30) 30
pregnancy (30) 30
beckwith-wiedemann syndrome (29) 29
research (28) 28
adolescent (27) 27
gene (27) 27
genetic testing (27) 27
imprinting (27) 27
child, preschool (26) 26
polymorphism, single nucleotide (26) 26
infant, newborn (25) 25
dna mutational analysis (24) 24
genetics (24) 24
base sequence (23) 23
fetal growth retardation - genetics (23) 23
young adult (23) 23
karyotyping (22) 22
pedigree (22) 22
alleles (21) 21
chromosomes, human, pair 11 - genetics (21) 21
growth (21) 21
analysis (20) 20
genes (20) 20
molecular sequence data (20) 20
neurosciences (20) 20
chromosome aberrations (19) 19
genetic disorders (19) 19
hypomethylation (19) 19
mosaicism (19) 19
silver-russell syndrome - diagnosis (19) 19
silver-russell-syndrome (19) 19
uniparental disomy - genetics (19) 19
beckwith-wiedemann syndrome - genetics (18) 18
cystinuria - genetics (18) 18
genotype & phenotype (18) 18
beckwith-wiedemann-syndrome (17) 17
identification (17) 17
middle aged (17) 17
region (17) 17
risk factors (17) 17
chromosome 11p15 (16) 16
chromosomes (16) 16
human genetics (16) 16
cohort studies (15) 15
diagnosis (15) 15
epigenetics (15) 15
fmri (15) 15
genetic variation (15) 15
heterozygote (15) 15
maternal uniparental disomy (15) 15
physiological aspects (15) 15
chromosomes, human, pair 11 (14) 14
genomes (14) 14
sequence analysis, dna (14) 14
trisomy (14) 14
urology & nephrology (14) 14
amino acid transport systems, basic - genetics (13) 13
disease (13) 13
genomic imprinting - genetics (13) 13
medicine, research & experimental (13) 13
microsatellite repeats (13) 13
polymorphism, genetic (13) 13
silver–russell syndrome (13) 13
article (12) 12
children (12) 12
chromosome deletion (12) 12
chromosomes, human, pair 14 - genetics (12) 12
endocrinology & metabolism (12) 12
gene mutations (12) 12
genetic counseling (12) 12
magnetic resonance imaging (12) 12
schizophrenia (12) 12
carrier proteins - genetics (11) 11
case-control studies (11) 11
dna (11) 11
epigenesis, genetic (11) 11
gene deletion (11) 11
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range

by Ehret, Georg B and Munroe, Patricia B and Rice, Kenneth M and Bochud, Murielle and Johnson, Anew D and Chasman, Daniel I and Smith, Albert V and Tobin, Martin D and Verwoert, Germaine C and Hwang, Shih-Jen and Pihur, Vasyl and Vollenweider, Peter and O'Reilly, Paul F and Amin, Najaf and Bragg-Gresham, Jennifer L and Teumer, Alexander and Glazer, Nicole L and Launer, Lenore and Zhao, Jing Hua and Aulchenko, Yurii and Heath, Simon and Sõber, Siim and Parsa, Afshin and Luan, Jian'an and Arora, Pankaj and Dehghan, Abbas and Zhang, Feng and Lucas, Gavin and Hicks, Anew A and Jackson, Anne U and Peden, John F and Tanaka, Toshiko and Wild, Sarah H and Rudan, Igor and Igl, Wilmar and Milaneschi, Yuri and Parker, Alex N and Fava, Cristiano and Chambers, John C and Fox, Ervin R and Kumari, Meena and Go, Min Jin and van der Harst, Pim and Kao, Wen Hong Linda and Sjögren, Marketa and Vinay, D. G and Alexander, Myriam and Tabara, Yasuharu and Shaw-Hawkins, Sue and Whincup, Peter H and Liu, Yongmei and Shi, Gang and Kuusisto, Johanna and Tayo, Bamidele and Seielstad, Mark and Sim, Xueling and Nguyen, Khanh-Dung Hoang and Lehtimäki, Terho and Matullo, Giuseppe and Wu, Ying and Gaunt, Tom R and Onland-Moret, N. Charlotte and Cooper, Matthew N and Platou, Carl G. P and Org, Elin and Hardy, Rebecca and Dahgam, Santosh and Palmen, Jutta and Vitart, Veronique and Braund, Peter S and Kuznetsova, Tatiana and Uiterwaal, Cuno S. P. M and Adeyemo, Adebowale and Palmas, Walter and Campbell, Harry and Ludwig, Barbara and Tomaszewski, Maciej and Tzoulaki, Ioanna and Palmer, Nicholette D and Aspelund, Thor and Garcia, Melissa and Chang, Yen-Pei C and O'Connell, Jeffrey R and Steinle, Nanette I and Grobbee, Diederick E and Arking, Dan E and Kardia, Sharon L and Morrison, Alanna C and Hernandez, Dena and Najjar, Samer and McArdle, Wendy L and Hadley, David and Brown, Morris J and Connell, John M and Hingorani, Aroon D and Day, Ian N. M and Lawlor, Debbie A and Beilby, John P and Lawrence, Robert W and Clarke, Robert and ... and CHARGE-HF Consortium and EchoGen Consortium and KidneyGen Consortium and CARDIoGRAM Consortium and Int Consortium Blood Pressure Geno and CKDGen Consortium and International Consortium for Blood Pressure Genome-Wide Association Studies and EchoGen consortium and CHARGE-HF consortium and CARDIoGRAM consortium and The International Consortium for Blood Pressure Genome-Wide Association Studies and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Uppsala universitet
Nature, ISSN 0028-0836, 2011, Volume 478, Issue 7367, pp. 103 - 109
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 09/2016, Volume 99, Issue 3, pp. 555 - 566
Journal Article
Journal Article
by Wain, Louise and Verwoert, Germaine and O'Reilly, Paul and Shi, Gang and Johnson, Toby and Bochud, Murielle and Rice, Kenneth and Henneman, Peter and Smith, Albert Vernon and Ehret, Georg and Amin, Najaf and Larson, Martin and Mooser, Vincent and Hadley, David and Dörr, Marcus and Bis, Joshua and Aspelund, Thor and Esko, Tõnu and Janssens, Cécile and Zhao, Jing Hua and Heath, Simon and Laan, Maris and Fu, Jingyuan and Pistis, Giorgio and Luan, J and Lucas, Gavin and Pirastu, Nicola and Pichler, Irene and Jackson, Anne and Webster, Rebecca J and Zhang, F.F and Peden, John and Schmidt, Reinhold and Tanaka, Toshiko and Campbell, Harry and Igl, Wilmar and Milaneschi, Yuri and Hottenga, Jouke Jan and Vitart, Veronique and Chasman, Daniel and Trompet, Stella and Bragg-Gresham, Jennifer L and Alizadeh, Behrooz and Chambers, John and Guo, Xiuqing and Lehtimäki, Terho and Kuhnel, Brigitte and Lopez, L.M and Polasek, Ozren and Boban, Mladen and Nelson, Christopher P and Morrison, Alanna and Pihur, Vasyl and Ganesh, Santhi and Hofman, Albert and Kundu, Suman and Mattace Raso, Francesco and Rivadeneira Ramirez, Fernando and Sijbrands, Eric and Uitterlinden, Ané and Hwang, S.J and Vasan, Ramachanan Srini and Wang, Ying and Bergmann, Sven and Vollenweider, Peter and Waeber, Gérard and Laitinen, Jaana and Pouta, Anneli and Zitting, Paavo and McArdle, Wendy and Kroemer, Heyo and Völker, Uwe and Völzke, Henry and Glazer, Nicole and Taylor, Kent and Harris, Tamara and Alavere, Helene and Haller, Toomas and Keis, Aime and Tammesoo, M.L and Aulchenko, Yurii and Khaw, Kay-Tee and Galan, Pilar and Hercberg, Serge and Lathrop, Mark and Eyheramendy, Susana and Org, Elin and Sõber, Siim and Lu, Xiaowen and Nolte, Ilja and Penninx, Brenda and Corre, Tanguy and Masciullo, Corrado and Sala, Cinzia and Groop, Leif and Voight, Benjamin and Melander, Olle and O'Donnell, Christopher and Salomaa, Veikko and Adamo, Pio and ... and CHARGE Consortium Heart Failure and Cardiogenics Consortium and AortaGen Consortium and LifeLines Cohort Study and EchoGen Consortium and KidneyGen Consortium and CKDGen Consortium and CardioGram and Cardiogenics consortium and KidneyGen consortium and CHARGE Consortium Heart Failure Working Group and EchoGen consortium and CKDGen consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Uppsala universitet
Nature Genetics, ISSN 1061-4036, 10/2011, Volume 43, Issue 10, pp. 1005 - 1012
Journal Article
by Wirtz and Fischer and Backhaus and Bergmann and Brandt and Heinrichs and Koenen and Schneider and Eggermann and Kurth and Stoppe and Bernhagen and Bruns and Berg and Trautwein and Berres
International Journal of Molecular Sciences, ISSN 1422-0067, 07/2019, Volume 20, Issue 15, p. 3753
Two polymorphisms in the promoter region of macrophage migration inhibitory factor (MIF)-rs755622 and rs5844572-exhibit prognostic relevance in inflammatory... 
Index Medicus | liver fibrosis | promoter polymorphisms | HCV | macrophage migration inhibitory factor | biomarker | hepatocellular carcinoma
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 11676 - 7
Replicative senescence hampers application of mesenchymal stromal cells (MSCs) because it limits culture expansion, impairs differentiation potential, and... 
TRANSFORMATION | DEFINED FACTORS | BIOMARKER | MULTIDISCIPLINARY SCIENCES | EXPANSION | SENESCENCE | INDUCTION | CULTURE | CANCER | DNA-METHYLATION | IPS CELLS | Cell culture | Transformation | Senescence | Media (culture) | Mesenchyme | Standardization | Chromosome 1 | Transfection | Plasmids | Immortalization | Stromal cells | Stem cells | DNA methylation | Epigenetics | Methylation | Pluripotency | Age | Inhibitory postsynaptic potentials
Journal Article