Jin Li
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Chinese geneticist
Jin Li's AcademicInfluence.com Rankings
Jin Libiology Degrees
Biology
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Genetics
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Molecular Biology
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Biology
Jin Li's Degrees
- Bachelors Biology Peking University
- Masters Genetics Peking University
- PhD Genetics Peking University
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Why Is Jin Li Influential?
(Suggest an Edit or Addition)According to Wikipedia, Jin Li is a Chinese geneticist and academic administrator, currently serving as president of Fudan University since 2021. Jin joined Fudan University from the University of Cincinnati in 2003 to serve as dean of the Fudan University School of Life Sciences. He previously served as the university's executive vice president from 2019 to 2021, vice president from 2007 to 2019, and dean of the Graduate School from 2007 to 2011.
Jin Li's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Application of dual affinity retargeting molecules to achieve optimal redirected T-cell killing of B-cell lymphoma. (2011) (237)
- Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella. (2017) (188)
- Effector cell recruitment with novel Fv-based dual-affinity re-targeting protein leads to potent tumor cytolysis and in vivo B-cell depletion. (2010) (170)
- A CD3xCD123 bispecific DART for redirecting host T cells to myelogenous leukemia: Preclinical activity and safety in nonhuman primates (2015) (127)
- Partial deletions are associated with an increased risk of complete deletion in AZFc: a new insight into the role of partial AZFc deletions in male infertility (2007) (99)
- The b2/b3 subdeletion shows higher risk of spermatogenic failure and higher frequency of complete AZFc deletion than the gr/gr subdeletion in a Chinese population. (2009) (88)
- Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice. (2019) (83)
- Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility. (2020) (78)
- Therapeutic control of B cell activation via recruitment of Fcgamma receptor IIb (CD32B) inhibitory function with a novel bispecific antibody scaffold. (2010) (70)
- Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella (2018) (63)
- A Frequent Partial AZFc Deletion does not Render an Increased Risk of Spermatogenic Impairment in East Asians (2006) (60)
- Efficient typing of copy number variations in a segmental duplication-mediated rearrangement hotspot using multiplex competitive amplification (2012) (57)
- TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model (2019) (55)
- Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility (2019) (52)
- Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice. (2020) (50)
- Cohort Profile: The Rugao Longevity and Ageing Study (RuLAS). (2015) (48)
- Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice. (2019) (47)
- Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility (2018) (47)
- MGD011, A CD19 x CD3 Dual-Affinity Retargeting Bi-specific Molecule Incorporating Extended Circulating Half-life for the Treatment of B-Cell Malignancies (2016) (47)
- Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAF (2020) (45)
- TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice (2018) (44)
- Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility. (2021) (43)
- Biallelic mutations in CFAP65 cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice (2019) (42)
- Evaluation of copy number variation detection for a SNP array platform (2014) (41)
- Rare variants in FANCA induce premature ovarian insufficiency (2019) (39)
- Agreement between the frailty index and phenotype and their associations with falls and overnight hospitalizations. (2016) (33)
- C-reactive protein, frailty and overnight hospital admission in elderly individuals: A population-based study. (2016) (29)
- Additional genomic duplications in AZFc underlie the b2/b3 deletion-associated risk of spermatogenic impairment in Han Chinese population. (2011) (27)
- Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia. (2019) (27)
- Common variants in the ATP2B1 gene are associated with hypertension and arterial stiffness in Chinese population (2013) (26)
- Visual impairment, but not hearing impairment, is independently associated with lower subjective well-being among individuals over 95 years of age: A population-based study. (2016) (23)
- Increased genome instability in human DNA segments with self-chains: homology-induced structural variations via replicative mechanisms. (2013) (22)
- Reliability and relative validity of three physical activity questionnaires in Taizhou population of China: the Taizhou Longitudinal Study. (2015) (22)
- CNV instability associated with DNA replication dynamics: evidence for replicative mechanisms in CNV mutagenesis. (2015) (21)
- Sleep disturbances and risk of falls in an old Chinese population-Rugao Longevity and Ageing Study. (2017) (20)
- Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype–phenotype correlations (2019) (20)
- Influences of APOA5 Variants on Plasma Triglyceride Levels in Uyghur Population (2014) (19)
- Risk factors of age‐related cataract in a Chinese adult population: the Taizhou Eye Study (2018) (19)
- Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause. (2020) (17)
- Association between subjective well-being and exceptional longevity in a longevity town in China: a population-based study (2014) (16)
- Replicative mechanisms of CNV formation preferentially occur as intrachromosomal events: evidence from Potocki-Lupski duplication syndrome. (2013) (16)
- Blood biomarkers and functional disability among extremely longevous individuals: a population-based study. (2015) (16)
- Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice (2019) (15)
- Use of serum albumin and activities of daily living to predict mortality in long-lived individuals over 95 years of age: a population-based study (2015) (15)
- Associations of triglyceride levels with longevity and frailty: A Mendelian randomization analysis (2017) (14)
- DAZ duplications confer the predisposition of Y chromosome haplogroup K* to non-obstructive azoospermia in Han Chinese populations. (2013) (14)
- Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome. (2015) (13)
- Conjugation of DM1 to anti-CD30 antibody has potential antitumor activity in CD30-positive hematological malignancies with lower systemic toxicity (2019) (13)
- Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome. (2020) (11)
- The association of Y chromosome haplogroups with spermatogenic failure in the Han Chinese (2007) (10)
- Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice (2021) (9)
- Increased half-life and enhanced potency of Fc-modified human PCSK9 monoclonal antibodies in primates (2017) (9)
- Genome-wide CNV analysis in mouse induced pluripotent stem cells reveals dosage effect of pluripotent factors on genome integrity (2014) (9)
- Joint utilization of genetic analysis and semi-cloning technology reveals a digenic etiology of Müllerian anomalies (2019) (9)
- Anemia, Physical Function, and Mortality in Long‐Lived Individuals Aged 95 and Older: A Population‐Based Study (2015) (9)
- Y chromosome haplogroups based genome-wide association study pinpoints revelation for interactions on non-obstructive azoospermia (2016) (8)
- MircroRNA-10b Promotes Human Embryonic Stem Cell-Derived Cardiomyocyte Proliferation via Novel Target Gene LATS1 (2019) (8)
- Association of Natriuretic Peptide Receptor-C Gene with Ischemic Stroke and Hypertension in Chinese Han Population (2012) (7)
- A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling (2022) (6)
- Prevalence and related factors of chronic kidney disease (CKD) among long-lived individuals (LLI) over 95 years of age. (2015) (6)
- Mitochondrial DNA sequencing and large-scale genotyping identifies MT-ND4 gene mutation m.11696G>A associated with idiopathic oligoasthenospermia (2017) (6)
- A heterozygous hypomorphic mutation of Fanca causes impaired follicle development and subfertility in female mice (2020) (5)
- Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility (2022) (5)
- Rearrangement structure-independent strategy of CNV breakpoint analysis (2014) (5)
- Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract (2019) (5)
- Novel Mutations in X-Linked, USP26-Induced Asthenoteratozoospermia and Male Infertility (2021) (4)
- Landscape of pathogenic mutations in premature ovarian insufficiency (2023) (4)
- Mitochondrial DNA Haplogroup M7 Confers Disability in a Chinese Aging Population (2020) (4)
- Association of immunity markers with the risk of incident frailty: the Rugao longitudinal aging study (2022) (3)
- 138 Preclinical activity and safety of MGD006, a CD123xCD3 Bispecific DART® molecule for the treatment of hematological malignancies (2014) (3)
- Temporal transcriptomic landscape of postnatal mouse ovaries reveals dynamic gene signatures associated with ovarian aging (2021) (3)
- T0001, a variant of TNFR2-Fc fusion protein, exhibits improved Fc effector functions through increased binding to membrane-bound TNFα (2017) (3)
- [Copy number variations in the human genome: their mutational mechanisms and roles in diseases]. (2011) (3)
- Prevalence, Causes, and Factors Associated with Visual Impairment in a Chinese Elderly Population: The Rugao Longevity and Aging Study (2021) (2)
- Human mitochondrial DNA haplogroup M8a influences the penetrance of m.8684C>T in Han Chinese men with non-obstructive azoospermia. (2018) (2)
- EIF4ENIF1 variants in two patients with non-syndromic premature ovarian insufficiency. (2022) (1)
- Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice (2021) (1)
- Corrigendum: Associations of triglyceride levels with longevity and frailty: A Mendelian randomization analysis (2017) (1)
- Genome-wide CNV analysis in mouse induced pluripotent stem cells reveals dosage effect of pluripotent factors on genome integrity (2014) (1)
- A homozygous frameshift mutation in ADAD2 cause male infertility with spermatogenic impairments. (2023) (1)
- Interaction between Y chromosome haplogroup O3* and 4-n-octylphenol exposure reduces the susceptibility to spermatogenic impairment in Han Chinese. (2017) (1)
- Frailty and the risk of kidney function decline in the elderly population: the Rugao Longevity and Ageing Study. (2021) (1)
- Phenotype correlations reveal the relationships of physiological systems underlying human ageing (2021) (1)
- Evaluation of copy number variation detection for a SNP array platform (2014) (1)
- Whole exome sequencing identified a rare WT1 loss‐of‐function variant in a non‐syndromic POI patient (2021) (1)
- Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype–phenotype correlations (2019) (0)
- Use of serum albumin and activities of daily living to predict mortality in long-lived individuals over 95 years of age: a population-based study (2015) (0)
- Joint utilization of genetic analysis and semi-cloning technology reveals a digenic etiology of Müllerian anomalies (2019) (0)
- Correction: A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling (2022) (0)
- MtDNA genomes reveal a relaxation of selective constraints in low-BMI individuals in a Uyghur population (2017) (0)
- Rearrangement structure-independent strategy of CNV breakpoint analysis (2014) (0)
- Association of immunity markers with the risk of incident frailty: the Rugao longitudinal aging study (2022) (0)
- T.129. Suppression of B Cell Activation by Inhibitory Receptor Signaling using Dual-Affinity Re-Targeting (DART) Molecules (2009) (0)
- A heterozygous hypomorphic mutation of Fanca causes impaired follicle development and subfertility in female mice (2020) (0)
- Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract (2019) (0)
- Comparative Performance of Creatinine-Based GFR Estimation Equations in Exceptional Longevity: The Rugao Longevity and Ageing Study [Erratum] (2020) (0)
- Common variants in the ATP2B1 gene are associated with hypertension and arterial stiffness in Chinese population (2012) (0)
- Negative modulation of B-cell function via inhibitory receptor signaling by using novel diabody-based Dual-Affinity Re-Targeting (DART) molecules (96.14) (2010) (0)
- Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility (2018) (0)
- Comparative Performance of Creatinine-Based GFR Estimation Equations in Exceptional Longevity: The Rugao Longevity and Ageing Study (2020) (0)
- Ganglion Cell-Inner Plexiform Layer Thickness is Associated with Persistently Cognitive Decline -The Rugao Longevity and Aging Study (2020) (0)
- Identification of rare and common variants of SIRT6 gene in long-lived individuals (2016) (0)
- The composite phenotype analysis identifies potential concerted responses of physiological systems to high altitude exposure (2023) (0)
- Plasma homocysteine and macular thickness in older adults—the Rugao Longevity and Aging Study (2021) (0)
- TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model (2019) (0)
- Large Population-Based Cohort Studies (2016) (0)
- HSD17B12 dosage insufficiency induced premature ovarian insufficiency in humans and mice (2022) (0)
- Association between subjective well-being and exceptional longevity in a longevity town in China: a population-based study (2014) (0)
- Mitochondrial genomes and exceptional longevity in a Chinese population: the Rugao longevity study (2015) (0)
- Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA. (2023) (0)
- Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models. (2023) (0)
- Association of Arterial Stiffness with Functional Disability and Mobility Limitation: The Rugao Longitudinal Ageing Study (2022) (0)
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