Sperm defects in primary ciliary dyskinesia and related causes of male infertility is a research paper published in Cellular and Molecular Life Sciences (2020). On theSindex it has a DataRank of 0.847. It has been cited 282 times.
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Base Score Contribution
0.847
From this paper's citation signal
Citation Network Contribution
0
Citation network not refreshed for this result
This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.
Learn more about DataRank methodology →H2020 Marie Skłodowska-Curie Actions
Grant: 800556
Identification of novel genes and mechanisms for PCD and male infertility
Great Ormond Street Hospital Charity
Grant: V2217
National Institute for Health Research
Grant: V1299
FWCI
21.30
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
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Additional file 1 of Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia
Additional file 2 of Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia
Additional file 2 of Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia
Additional file 3 of Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia
Additional file 3 of Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia
Additional file 4 of Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia
Additional file 4 of Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia
Additional file 5 of Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia
Additional file 5 of Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia
Additional file 6 of Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia
Additional file 6 of Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia
Additional file 1 of Exploiting genomic synteny in Felidae: cross-species genome alignments and SNV discovery can aid conservation management
Additional file 1 of Exploiting genomic synteny in Felidae: cross-species genome alignments and SNV discovery can aid conservation management
Additional file 1 of Biallelic mutations of TTC12 and TTC21B were identified in Chinese patients with multisystem ciliopathy syndromes
Additional file 1 of Biallelic mutations of TTC12 and TTC21B were identified in Chinese patients with multisystem ciliopathy syndromes
Additional file 4 of Biallelic mutations of TTC12 and TTC21B were identified in Chinese patients with multisystem ciliopathy syndromes
Additional file 4 of Biallelic mutations of TTC12 and TTC21B were identified in Chinese patients with multisystem ciliopathy syndromes
Additional file 5 of Biallelic mutations of TTC12 and TTC21B were identified in Chinese patients with multisystem ciliopathy syndromes
Additional file 5 of Biallelic mutations of TTC12 and TTC21B were identified in Chinese patients with multisystem ciliopathy syndromes