ScholarIQanswers from OpenAlex
Molecular Genetics & Genomic Medicine
JournalCitation impact & published research
Molecular Genetics & Genomic Medicine is a journal indexed in ScholarIQ from OpenAlex.
How many works does Molecular Genetics & Genomic Medicine have?
ScholarIQindexed works
Molecular Genetics & Genomic Medicine has 2,886 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Molecular Genetics & Genomic Medicine have?
ScholarIQcitation count
Molecular Genetics & Genomic Medicine has 33,382 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Molecular Genetics & Genomic Medicine?
ScholarIQh-index
Molecular Genetics & Genomic Medicine has an h-index of 58 in OpenAlex.
What is the article processing charge of Molecular Genetics & Genomic Medicine?
ScholarIQarticle processing charge
Molecular Genetics & Genomic Medicine lists an article processing charge of 2,700 USD in OpenAlex.
What is the OpenAlex record for Molecular Genetics & Genomic Medicine?
ScholarIQopenalex
The OpenAlex for Molecular Genetics & Genomic Medicine is on the source record.
What are the most-cited papers on Molecular Genetics & Genomic Medicine?
ScholarIQmost cited works
Current status of beta‐thalassemia and its treatment strategies
Shaukat Ali, Shumaila Mumtaz, Hafiz Abdullah Shakir, Muhammad Ali Khan, Hafiz Muhammad Tahir, Samaira Mumtaz, Tafail Akbar Mughal, Ali Hassan, Syed Akif Raza Kazmi, Sadia Sadia, Muhammad Irfan, Muhammad Adeeb Khan
Integrated bioinformatics analysis of key genes involved in progress of colon cancer
Haojie Yang, Jiong Wu, Jingjing Zhang, Zhigang Yang, Wei Jin, Ying Li, Jin Lei, Lu Yin, Hua Liu, Zhenyi Wang
Evaluation of copy number variant detection from panel‐based next‐generation sequencing data
Ruen Yao, Tingting Yu, Yanrong Qing, Jian Wang, Yiping Shen
Homozygous <i>GDF2</i> nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an “HHT‐like” syndrome in children
Joshua Hodgson, Lı́dia Ruiz, Jamie McDonald, Oliver Quarrell, Kelechi Ugonna, James R. Bentham, Rebecca S. Mason, Jennifer M. Martin, David Moore, Katie Bergstrom, Pınar Bayrak‐Toydemir, Whitney Wooderchak‐Donahue, Nicholas W. Morrell, Robin Condliffe, Carmelo Bernabéu, Paul D. Upton
Genotype–phenotype investigation of 35 patients from 11 unrelated families with camptodactyly–arthropathy–coxa vara–pericarditis (<scp>CACP</scp>) syndrome
Saliha Yılmaz, Dilek Uludağ Alkaya, Özgür Kasapçopur, Kenan Barut, Ekin Su Akdemir, Cemre Celen, Mark W. Youngblood, Katsuhito Yasuno, Kaya Bilgüvar, Murat Günel, Beyhan Tüysüz