| scholarly article | Q13442814 |
| P8978 | DBLP publication ID | journals/jbcb/OLearyDSBKAGBLACSCSSB07 |
| P356 | DOI | 10.1142/S0219720007003132 |
| P698 | PubMed publication ID | 18172923 |
| P50 | author | Edwin M. Stone | Q37381855 |
| Todd E. Scheetz | Q55283736 | ||
| Val C. Sheffield | Q61268600 | ||
| P2093 | author name string | Abbot F Clark | |
| Thomas L Casavant | |||
| Michael F Smith | |||
| Terry A Braun | |||
| Thomas Burns | |||
| Bartley Brown | |||
| Hakeem Almabrazi | |||
| Brian M O'Leary | |||
| Vladimir Leontiev | |||
| Jason A Grundstad | |||
| Jeaneen Andorf | |||
| Mathew B Kemp | |||
| Steven G Davis | |||
| P2860 | cites work | Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3) | Q24533582 |
| The Ensembl genome database project | Q24548408 | ||
| POCUS: mining genomic sequence annotation to predict disease genes | Q24793367 | ||
| SIFT: Predicting amino acid changes that affect protein function | Q29547211 | ||
| Prediction of deleterious human alleles | Q29614367 | ||
| Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease | Q29619085 | ||
| A model recognition approach to the prediction of all-helical membrane protein structure and topology | Q30420917 | ||
| Genome-wide identification of pseudogenes capable of disease-causing gene conversion. | Q34521369 | ||
| Approaches to identify genes for complex human diseases: lessons from Mendelian disorders | Q35211717 | ||
| Conformation sensitive gel electrophoresis for simple and accurate detection of mutations: comparison with denaturing gradient gel electrophoresis and nucleotide sequencing | Q35881881 | ||
| Coding single-nucleotide polymorphisms associated with complex vs. Mendelian disease: evolutionary evidence for differences in molecular effects. | Q37585393 | ||
| Improvements in protein secondary structure prediction by an enhanced neural network | Q41234964 | ||
| Human Gene Mutation Database (HGMD): 2003 update | Q47903166 | ||
| Prioritizing regions of candidate genes for efficient mutation screening. | Q51293029 | ||
| P433 | issue | 6 | |
| P921 | main subject | prioritization | Q11888847 |
| P304 | page(s) | 1155-1172 | |
| P577 | publication date | 2007-12-01 | |
| P1433 | published in | Journal of Bioinformatics and Computational Biology | Q6294841 |
| P1476 | title | Transcript annotation prioritization and screening system (TrAPSS) for mutation screening | |
| P478 | volume | 5 |
| Q41458680 | Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomaly | cites work | P2860 |
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