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Research article

First published 2004-2

Indexing Anatomical Concepts to OMIM Clinical Synopsis Using the UMLS Metathesaurus

Teruyoshi Hishiki, Osamu Ogasawara, Yoshimasa Tsuruoka [...]

In Silico Biology

Open access

Research article

First published 2006

Application of a New Probabilistic Model for Mining Implicit Associated Cancer Genes from OMIM and Medline

Shanfeng Zhu, Yasushi Okuno, Gozoh Tsujimoto [...]

Cancer Informatics

Free access

Research article

First published 2013-4

[Omim][BF 4 ] Ionic Liquid,a Green and Recyclable Medium for One-pot Aminomethylation of Electron-rich Aromatic Compounds

Amene Yaghoubi Arzephoni, M. Reza Naimi-Jamal, Ali Sharifi [...]

Journal of Chemical Research

Free access

Research article

First published 2008-2

BioCompass: A Novel Functional Inference Tool that Utilizes MeSH Hierarchy to Analyze Groups of Genes

Takeru Nakazato, Toru Takinaka, Hironori Mizuguchi [...]

In Silico Biology

Free access

Research article

First published 2006-7

Huge Proteins in The Human Proteome and Their Participation in Hereditary Diseases

Meena Kishore Sakharkar, Pandjassarame Kangueane, Kishore Ramaji Sakharkar [...]

In Silico Biology

Retricted access

Research article

First published 2015-1

The Molecular Basis of Hereditary Enamel Defects in Humans

J.T. Wright, I.A. Carrion, C. Morris

Journal of Dental Research

Retricted access

Research article

First published

Metabolic Flux Correlations,Genetic Interactions,and Disease

Balaji Veeramani, Joel S. Bader

Journal of Computational Biology

Open access

Research article

First published 2023

Lipoid Congenital Adrenal Hyperplasia With a Novel StAR Gene Mutation

Ayman A Bakkar, Abdulaziz Alsaedi, Naglaa M Kamal [...]

Clinical Medicine Insights: Endocrinology and Diabetes

Retricted access

Case report

First published 2015-3

Craniofrontonasal Syndrome: Atrial Septal Defect with a Novel EFNB1 Gene Mutation

Manisha Goyal, Gaurav Pradhan, Ilse Wieland [...]

The Cleft Palate Craniofacial Journal

Open access

Case report

First published 2023

A case of Chopra-Amiel-Gordon syndrome with a novel heterozygous variant in the ANKRD17 gene: A case report

Tkemaladze Tinatin, Bregvadze Kakha, Gogoberishvili Mikheil [...]

Sage Open Medical Case Reports

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