Zain Bassam Mohammad DARDAS
Concepts are derived automatically from a person's publications.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
| Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
|---|
| Heterotaxy Syndrome | 1 | 2024 | 63 | 0.880 |
Why?
|
| Transposition of Great Vessels | 1 | 2024 | 133 | 0.840 |
Why?
|
| Dysferlin | 1 | 2020 | 4 | 0.700 |
Why?
|
| Muscular Dystrophies | 1 | 2020 | 62 | 0.680 |
Why?
|
| Retinal Dystrophies | 3 | 2021 | 11 | 0.520 |
Why?
|
| Heart Defects, Congenital | 2 | 2024 | 1796 | 0.490 |
Why?
|
| Consanguinity | 3 | 2020 | 116 | 0.360 |
Why?
|
| Jordan | 4 | 2020 | 25 | 0.300 |
Why?
|
| Pedigree | 5 | 2021 | 2040 | 0.250 |
Why?
|
| Niemann-Pick Disease, Type C | 1 | 2022 | 5 | 0.210 |
Why?
|
| Arteries | 1 | 2024 | 288 | 0.200 |
Why?
|
| Nod2 Signaling Adaptor Protein | 1 | 2022 | 25 | 0.200 |
Why?
|
| Musculoskeletal Abnormalities | 1 | 2022 | 77 | 0.200 |
Why?
|
| Comparative Genomic Hybridization | 1 | 2024 | 688 | 0.190 |
Why?
|
| Scimitar Syndrome | 1 | 2022 | 53 | 0.190 |
Why?
|
| Membrane Transport Proteins | 1 | 2022 | 248 | 0.190 |
Why?
|
| Hearing Loss, Sensorineural | 1 | 2022 | 155 | 0.190 |
Why?
|
| T-Box Domain Proteins | 1 | 2022 | 154 | 0.190 |
Why?
|
| Genetic Variation | 2 | 2020 | 2157 | 0.190 |
Why?
|
| Heart Septal Defects, Atrial | 1 | 2022 | 128 | 0.180 |
Why?
|
| Exome | 3 | 2021 | 1249 | 0.180 |
Why?
|
| Phenotype | 5 | 2024 | 6502 | 0.180 |
Why?
|
| Malabsorption Syndromes | 1 | 2020 | 46 | 0.170 |
Why?
|
| Cystic Fibrosis | 1 | 2022 | 291 | 0.170 |
Why?
|
| Biliary Atresia | 1 | 2022 | 206 | 0.170 |
Why?
|
| Retinitis Pigmentosa | 1 | 2020 | 85 | 0.170 |
Why?
|
| Abnormalities, Multiple | 2 | 2022 | 1023 | 0.170 |
Why?
|
| Mutation | 6 | 2022 | 15917 | 0.160 |
Why?
|
| Crohn Disease | 1 | 2022 | 329 | 0.160 |
Why?
|
| ATP-Binding Cassette Transporters | 1 | 2020 | 317 | 0.150 |
Why?
|
| Genetic Markers | 1 | 2021 | 1073 | 0.150 |
Why?
|
| Neurodevelopmental Disorders | 1 | 2022 | 461 | 0.150 |
Why?
|
| Receptor, Notch1 | 1 | 2019 | 216 | 0.140 |
Why?
|
| Microtubule-Associated Proteins | 1 | 2020 | 525 | 0.140 |
Why?
|
| Phosphotransferases (Alcohol Group Acceptor) | 1 | 2018 | 143 | 0.140 |
Why?
|
| DNA Copy Number Variations | 1 | 2024 | 1576 | 0.140 |
Why?
|
| Software | 1 | 2024 | 1357 | 0.140 |
Why?
|
| Basic Helix-Loop-Helix Transcription Factors | 1 | 2020 | 626 | 0.140 |
Why?
|
| Diarrhea | 1 | 2020 | 722 | 0.130 |
Why?
|
| Precursor T-Cell Lymphoblastic Leukemia-Lymphoma | 1 | 2019 | 332 | 0.120 |
Why?
|
| Intellectual Disability | 1 | 2022 | 1064 | 0.120 |
Why?
|
| Genetic Testing | 2 | 2022 | 1692 | 0.120 |
Why?
|
| Mutation, Missense | 1 | 2020 | 1196 | 0.120 |
Why?
|
| Genetic Predisposition to Disease | 3 | 2021 | 5777 | 0.100 |
Why?
|
| Nerve Tissue Proteins | 1 | 2020 | 1581 | 0.100 |
Why?
|
| Carrier Proteins | 1 | 2020 | 2085 | 0.100 |
Why?
|
| Homozygote | 2 | 2024 | 771 | 0.080 |
Why?
|
| DNA | 1 | 2018 | 3041 | 0.080 |
Why?
|
| Membrane Proteins | 1 | 2020 | 2922 | 0.080 |
Why?
|
| Humans | 14 | 2024 | 270713 | 0.080 |
Why?
|
| Genetic Association Studies | 2 | 2022 | 1098 | 0.070 |
Why?
|
| Young Adult | 3 | 2021 | 22243 | 0.070 |
Why?
|
| Leukemia, Lymphocytic, Chronic, B-Cell | 1 | 2019 | 2488 | 0.070 |
Why?
|
| Adolescent | 3 | 2021 | 32689 | 0.060 |
Why?
|
| Child | 3 | 2021 | 30560 | 0.060 |
Why?
|
| Female | 8 | 2022 | 148885 | 0.050 |
Why?
|
| DNA Mutational Analysis | 2 | 2020 | 2356 | 0.050 |
Why?
|
| Adult | 5 | 2021 | 82041 | 0.050 |
Why?
|
| Biological Variation, Population | 1 | 2022 | 28 | 0.050 |
Why?
|
| Qa-SNARE Proteins | 1 | 2022 | 41 | 0.050 |
Why?
|
| Male | 7 | 2021 | 128479 | 0.050 |
Why?
|
| Cystic Fibrosis Transmembrane Conductance Regulator | 1 | 2022 | 54 | 0.050 |
Why?
|
| Sphingomyelin Phosphodiesterase | 1 | 2022 | 48 | 0.050 |
Why?
|
| Upper Extremity Deformities, Congenital | 1 | 2022 | 6 | 0.050 |
Why?
|
| Lower Extremity Deformities, Congenital | 1 | 2022 | 10 | 0.050 |
Why?
|
| Endoribonucleases | 1 | 2022 | 120 | 0.050 |
Why?
|
| Phosphoprotein Phosphatases | 1 | 2022 | 221 | 0.050 |
Why?
|
| Genotype | 2 | 2020 | 4248 | 0.050 |
Why?
|
| Rare Diseases | 1 | 2024 | 360 | 0.050 |
Why?
|
| Fundus Oculi | 1 | 2020 | 69 | 0.040 |
Why?
|
| Electroretinography | 1 | 2020 | 128 | 0.040 |
Why?
|
| Animals | 1 | 2024 | 61357 | 0.040 |
Why?
|
| RNA Splicing | 1 | 2020 | 362 | 0.040 |
Why?
|
| Protein Domains | 1 | 2019 | 317 | 0.040 |
Why?
|
| Adaptor Proteins, Signal Transducing | 1 | 2024 | 1462 | 0.040 |
Why?
|
| Homeodomain Proteins | 1 | 2022 | 1124 | 0.040 |
Why?
|
| RNA-Binding Proteins | 1 | 2022 | 1016 | 0.030 |
Why?
|
| Cytoplasm | 1 | 2019 | 702 | 0.030 |
Why?
|
| Family | 1 | 2020 | 782 | 0.030 |
Why?
|
| Binding Sites | 1 | 2020 | 2249 | 0.030 |
Why?
|
| Visual Acuity | 1 | 2020 | 867 | 0.030 |
Why?
|
| Tomography, Optical Coherence | 1 | 2020 | 552 | 0.030 |
Why?
|
| Cell Nucleus | 1 | 2019 | 1715 | 0.030 |
Why?
|
| Middle Aged | 4 | 2021 | 90533 | 0.030 |
Why?
|
| DNA-Binding Proteins | 1 | 2022 | 4992 | 0.020 |
Why?
|
| Infant, Newborn | 1 | 2022 | 8603 | 0.020 |
Why?
|
| Transcription Factors | 1 | 2022 | 5415 | 0.020 |
Why?
|
| Cohort Studies | 1 | 2021 | 9463 | 0.020 |
Why?
|
| Infant | 1 | 2020 | 13994 | 0.010 |
Why?
|
| Child, Preschool | 1 | 2021 | 17072 | 0.010 |
Why?
|