X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (237) 237
index medicus (194) 194
male (140) 140
genetics & heredity (127) 127
female (124) 124
article (113) 113
genetics (92) 92
aged (81) 81
middle aged (77) 77
genomics (75) 75
adult (65) 65
genotype (62) 62
research (61) 61
risk factors (57) 57
polymorphism, single nucleotide (48) 48
genome-wide association (47) 47
genetic aspects (45) 45
genetic predisposition to disease (45) 45
phenotype (45) 45
risk (45) 45
aged, 80 and over (41) 41
genome-wide association study (41) 41
electronic health records (40) 40
genomes (39) 39
incidental findings (37) 37
medical genetics (37) 37
genetic research (35) 35
medicine (35) 35
analysis (34) 34
genetic variation (33) 33
genes (32) 32
cardiac & cardiovascular systems (31) 31
abridged index medicus (28) 28
case-control studies (27) 27
electronic medical records (27) 27
mutation (26) 26
population (25) 25
biochemistry & molecular biology (24) 24
exome (24) 24
genome, human (24) 24
surgery (24) 24
usage (24) 24
alleles (23) 23
cardiovascular disease (23) 23
lipids (23) 23
children (22) 22
disease (22) 22
genetic testing (22) 22
pedigree (22) 22
atherosclerosis (21) 21
cohort studies (21) 21
genetic linkage (21) 21
infant (21) 21
association (20) 20
child (20) 20
epidemiology (20) 20
medical records (20) 20
medical research (20) 20
research article (20) 20
respiratory system (20) 20
united states (20) 20
cancer (19) 19
prospective studies (19) 19
variants (19) 19
adolescent (18) 18
cholesterol (18) 18
coronary-heart-disease (18) 18
dna sequencing (18) 18
european continental ancestry group - genetics (18) 18
expression (18) 18
genetic disorders (18) 18
human genetics (18) 18
multidisciplinary sciences (18) 18
studies (18) 18
electronic medical-records (17) 17
gene frequency (17) 17
genetic predisposition to disease - genetics (17) 17
linkage analysis (17) 17
loci (17) 17
medical and health sciences (17) 17
medicin och hälsovetenskap (17) 17
nucleotide sequencing (17) 17
physiological aspects (17) 17
polymorphism, single nucleotide - genetics (17) 17
congenital heart disease (16) 16
peripheral vascular disease (16) 16
child, preschool (15) 15
common variants (15) 15
infant, newborn (15) 15
proteins (15) 15
single nucleotide polymorphisms (15) 15
algorithms (14) 14
alzheimer disease - genetics (14) 14
body mass index (14) 14
cardiovascular diseases - genetics (14) 14
chromosome mapping (14) 14
emerge network (14) 14
gene (14) 14
genome sequencing (14) 14
genotype & phenotype (14) 14
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


American Journal of Human Genetics, ISSN 0002-9297, 03/2017, Volume 100, Issue 3, p. 401
  Dr Stan Gartler is the winner of the 2016 McKusick Leadership Award of the American Society of Human Genetics. He was interested in human variation and has... 
Awards & honors | Genetics | Scientists | Chromosomes
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 3/2017, Volume 100, Issue 3, pp. 401 - 402
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 03/2017, Volume 100, Issue 3, pp. 401 - 402
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 03/2017, Volume 100, Issue 3, pp. 401 - 402
Journal Article
Genetics in medicine : official journal of the American College of Medical Genetics, ISSN 1098-3600, 04/2018, Volume 20, Issue 5, pp. 477 - 479
Journal Article
Genetics in Medicine, ISSN 1098-3600, 05/2018, Volume 20, Issue 5, pp. 531 - 535
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2016, Volume 98, Issue 6, pp. 1077 - 1081
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 06/2016, Volume 98, Issue 6, p. 1077
  The American College of Medical Genetics and Genomics (ACMG) and Association of Molecular Pathology (AMP) recently published important new guidelines aiming... 
Pathology | Genomics | Classification
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 06/2015, Volume 372, Issue 23, pp. 2258 - 2264
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 03/2018, Volume 102, Issue 3, pp. 335 - 339
Journal Article
Chemico-Biological Interactions, ISSN 0009-2797, 11/2016, Volume 259, Issue Pt B, pp. 51 - 62
Paraoxonase-1 (PON1), an esterase/lactonase primarily associated with plasma high-density lipoprotein (HDL), was the first member of this family of enzymes to... 
Oxidative stress | Paraoxonases | Human disease | Organophosphate | Anti-inflammatory | BIOCHEMISTRY & MOLECULAR BIOLOGY | LOW-DENSITY-LIPOPROTEIN | CHLORPYRIFOS-OXON | IN-VIVO | PHARMACOLOGY & PHARMACY | HUMAN-SERUM PARAOXONASE | ENDOPLASMIC-RETICULUM | TOXICOLOGY | SIGNAL N-(3-OXODODECANOYL)-L-HOMOSERINE LACTONE | ISCHEMIC-STROKE | CORONARY-ARTERY-DISEASE | PARKINSONS-DISEASE | Mitochondria - enzymology | Oxidative Stress | Ticlopidine - therapeutic use | Lipoproteins, HDL - blood | Humans | Male | Neurons - cytology | Homocysteine - metabolism | Homocysteine - analogs & derivatives | Organophosphorus Compounds - metabolism | Female | Neurons - metabolism | Aryldialkylphosphatase - deficiency | Platelet Aggregation Inhibitors - therapeutic use | Carotid Artery Diseases - metabolism | Carotid Artery Diseases - drug therapy | Astrocytes - cytology | Endoplasmic Reticulum - enzymology | Carotid Artery Diseases - etiology | Quorum Sensing | Cells, Cultured | Genotype | Inflammation | Aryldialkylphosphatase - genetics | Aryldialkylphosphatase - metabolism | Ticlopidine - analogs & derivatives | Mice, Knockout | Animals | Mice | Lipid Metabolism - physiology | Astrocytes - metabolism | Animal experimentation | Enzymes | Neurosciences | Gallstones | Insecticides | Development and progression | Antioxidants | Prevention | Metabolites | Analysis | Atherosclerosis | Medical genetics | Physiological aspects | Cancer
Journal Article
Value in Health, ISSN 1098-3015, 11/2019, Volume 22, Issue 11, pp. 1231 - 1239
Journal Article
Journal Article
SPINE, ISSN 0362-2436, 09/2019, Volume 44, Issue 17, pp. 1220 - 1227
STUDY DESIGN.A longitudinal cotwin control study of the Vietnam Era Twin Registry. OBJECTIVE.The aim of this study was to examine the association of... 
Psychological aspects | Complications and side effects | Aged men | Veterans | Post-traumatic stress disorder | Twins | Backache | Health aspects | Chronic pain | Risk factors
Journal Article
Genetics in Medicine, ISSN 1098-3600, 04/2018, Volume 20, Issue 5, pp. 531 - 535
This article provides a brief introduction to the Health Insurance Portability and Accountability Act of 1996 (HIPAA) Privacy Rule's minimum necessary... 
genomic data sharing | treatment uses | HIPAA Privacy Rule | minimum necessary standard | research | GENETICS & HEREDITY | Privacy | Health Insurance Portability & Accountability Act 1996-US | Laboratories | Information sharing
Journal Article
Genetics in Medicine, ISSN 1098-3600, 11/2013, Volume 15, Issue 11, pp. 854 - 859
The American College of Medical Genetics and Genomics recently issued recommendations for reporting incidental findings from clinical whole-genome sequencing... 
MANAGEMENT | BLOOD-PRESSURE | PROGRAM | DISEASE | GENETICS & HEREDITY | Genetic Predisposition to Disease | Genetic Testing | Patient Rights | Genomics | Humans | Incidental Findings | Penetrance | Patient Preference | Sequence Analysis, DNA | Exome | Genetics, Medical | Adult | Genome, Human | Child | Practice Guidelines as Topic
Journal Article
by Crosby, Jacy and Peloso, Gina M and Auer, Paul L and Crosslin, David R and Stitziel, Nathan O and Lange, Leslie A and Lu, Yingchang and Tang, Zheng-Zheng and Zhang, He and Hindy, George and Masca, Nicholas and Stirrups, Kathleen and Kanoni, Stavroula and Do, Ron and Jun, Goo and Hu, Youna and Kang, Hyun Min and Xue, Chenyi and Goel, Anuj and Farrall, Martin and Duga, Stefano and Merlini, Pier Angelica and Asselta, Rosanna and Girelli, Domenico and Olivieri, Oliviero and Martinelli, Nicola and Yin, Wu and Reilly, Dermot and Speliotes, Elizabeth and Fox, Caroline S and Hveem, Kristian and Holmen, Oddgeir L and Nikpay, Majid and Farlow, Deborah N and Assimes, Themistocles L and Franceschini, Nora and Robinson, Jennifer and North, Kari E and Martin, Lisa W and DePristo, Mark and Gupta, Namrata and Escher, Stefan A and Jansson, Jan-Håkan and Van Zuydam, Natalie and Palmer, Colin N. A and Wareham, Nicholas and Koch, Werner and Meitinger, Thomas and Peters, Annette and Lieb, Wolfgang and Erbel, Raimund and Konig, Inke R and Kruppa, Jochen and Degenhardt, Franziska and Gottesman, Omri and Bottinger, Erwin P and O'Donnell, Christopher J and Psaty, Bruce M and Ballantyne, Christie M and Abecasis, Goncalo and Ordovas, Jose M and Melander, Olle and Watkins, Hugh and Orho-Melander, Marju and Ardissino, Diego and Loos, Ruth J. F and McPherson, Ruth and Willer, Cristen J and Erdmann, Jeanette and Hall, Alistair S and Samani, Nilesh J and Deloukas, Panos and Schunkert, Heribert and Wilson, James G and Kooperberg, Charles and Rich, Stephen S and Tracy, Russell P and Lin, Dan-Yu and Altshuler, David and Gabriel, Stacey and Nickerson, Deborah A and Jarvik, Gail P and Cupples, L. Adrienne and Reiner, Alex P and Boerwinkle, Eric and Kathiresan, Sekar and The TG and HDL Working Group of the Exome Sequencing Project, National Heart, Lung, and Blood Institute and Natl Heart Lung Blood Inst and Exome Sequencing Project and TG and HDL Working Group of the Exome Sequencing Project, National Heart, Lung, and Blood Institute and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet and Medicin
The New England Journal of Medicine, ISSN 0028-4793, 07/2014, Volume 371, Issue 1, pp. 22 - 31
Journal Article