Eleanor Feingold

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 39 papers. Top paper: “Comparison of amyloid burden in individuals with Down syndrome versus autosomal dominant Alzheimer's disease: a cross-sectional study”.

Comparison of amyloid burden in individuals with Down syndrome versus autosomal dominant Alzheimer's disease: a cross-sectional study

The Lancet Neurology(2022)10.1016/s1474-4422(22)00408-2

N/A

1.1DataRank · unranked

56 citations

Brian A. Gordon, Julie K. Wisch, Shaney Flores, Rachel L. Henson, Omar H. Butt +95 more

A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals

Genetic Epidemiology(2019)10.1002/gepi.22214

N/A

0.593DataRank · unranked

51 citations

Deepti Anand, Azeez Butali, Carmen J. Buxo, Kaare Christensen, Frederic Deleyiannis +16 more

Comparison of tau spread in people with Down syndrome versus autosomal-dominant Alzheimer's disease: a cross-sectional study

The Lancet Neurology(2024)10.1016/s1474-4422(24)00084-x

N/A

0.542DataRank · unranked

36 citations

Nicole S. McKay, Anna H. Boerwinkle, James L. Kennedy, Shaney Flores, Benjamin L. Handen +86 more

Cerebrovascular disease is associated with Alzheimer’s plasma biomarker concentrations in adults with Down syndrome

Brain Communications(2024)10.1093/braincomms/fcae331

N/A

0.510DataRank · unranked

29 citations

Patrick J. Lao, Mohamad J. Alshikho, Olivia M. Ericsson, Batool Rizvi, Melissa Petersen +70 more

Timeline to symptomatic Alzheimer's disease in people with Down syndrome as assessed by amyloid-PET and tau-PET: a longitudinal cohort study

The Lancet Neurology(2024)10.1016/s1474-4422(24)00426-5

N/A

0.505DataRank · unranked

28 citations

Matthew Zammit, Jiebiao Wang, Benjamin L. Handen, Tobey J. Betthauser, Charles M. Laymon +71 more

Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects

Journal of Alzheimer s Disease(2022)10.3233/jad-220293

N/A

0.464DataRank · unranked

21 citations

Kang-Hsien Fan, Muhammad Aslam, Beth E. Snitz, Steven T. DeKosky, Oscar L. López +3 more

Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk

Frontiers in Cell and Developmental Biology(2022)10.3389/fcell.2022.621261

N/A

0.371DataRank · unranked

9 citations

John R. Shaffer, Fred Deleyiannis, Jacqueline T. Hecht, George L. Wehby, Kaare Christensen +5 more

A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals

10.1101/332270

N/A

0.292DataRank · unranked

6 citations

Deepti Anand, Azeez Butali, Carmen J. Buxo, Kaare Christensen, Frederic Deleyiannis +16 more

The PAX1 locus at 20p11 is a modifier for bilateral cleft lip only

medRxiv(2020)10.1101/2020.11.30.20241141

N/A

0.104DataRank · unranked

1 citations

Daniel Chang, Myoung Keun Lee, John R. Shaffer, Karlijne Indencleef, Michael P. Epstein +10 more

Variants in CALD1, ESRP1, and RBFOX1 are associated with orofacial cleft risk

PLoS Genetics(2025)10.1371/journal.pgen.1011581

N/A

0.104DataRank · unranked

1 citations

Xinyi Zhang, Zeynep Erdogan-Yildirim, Terri H. Beaty, Azeez Butali, Carmen J. Buxó +14 more

Limb development genes underlie variation in human fingerprint patterns

Cell(2022)10.1016/j.cell.2021.12.008

N/A

0DataRank · unranked

69 citations

James D. Glover, Haiguo Zhang, Meifang Peng, Jingze Tan, Chandana Basu Mallick +41 more

Association of Early Childhood Caries with Bitter Taste Receptors: A Meta-Analysis of Genome-Wide Association Studies and Transcriptome-Wide Association Study

Genes(2022)10.3390/genes14010059

N/A

0DataRank · unranked

19 citations

Tom Dudding, Jonathan M. Chernus, Rasha N. Alotaibi, Simon Haworth, Richard J. Crout +11 more

Genome‐wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes

Genetic Epidemiology(2022)10.1002/gepi.22447

N/A

0DataRank · unranked

14 citations

Eleanor Feingold, Lina Moreno‐Uribe, George L. Wehby, Luz Consuelo Valencia‐Ramirez, Claudia P. Restrepo Muñeton +16 more

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting

medRxiv(2022)10.1101/2022.08.15.22278795

N/A

0DataRank · unranked

2 citations

Sarah W. Curtis, Alba Sanchis-Juan, Xuefang Zhao, S. Taylor Head, Samantha Ho +18 more

Genomic landscape of Down syndrome-associated acute lymphoblastic leukemia

Blood(2023)10.1182/blood.2023019765

N/A

0DataRank · unranked

44 citations

Ti‐Cheng Chang, Jacob J. Junco, Meenakshi Devidas, Yizhen Li, Wenjian Yang +23 more

Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.05.018

N/A

0DataRank · unranked

97 citations

Kimberly K. Diaz Perez, Miranda Sun, Samantha Ho, Pankaj Chopra, Nandita Mukhopadhyay +22 more

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting

Genetics in Medicine(2023)10.1016/j.gim.2023.100918

N/A

0DataRank · unranked

22 citations

Sarah W. Curtis, Alba Sanchis-Juan, Xuefang Zhao, S. Taylor Head, Samantha Ho +18 more

Alzheimer's polygenic risk scores are associated with cognitive phenotypes in Down syndrome

Alzheimer s & Dementia(2023)10.1002/alz.13506

N/A

0DataRank · unranked

13 citations

Muhammad Aslam, Lam‐Ha T. Dang, Laura Xicota, María Victoria Fernández, Yun Ju Sung +16 more

Meta‐analysis of age‐related cognitive decline reveals a novel locus for the attention domain and implicates a COVID‐19‐related gene for global cognitive function

Alzheimer s & Dementia(2023)10.1002/alz.13064

N/A

0DataRank · unranked

10 citations

Kang‐Hsien Fan, Beth E. Snitz, Mary Ganguli, Steven T. DeKosky, Oscar L. López +3 more

DNA methylation and 28-year cardiovascular disease risk in type 1 diabetes: the Epidemiology of Diabetes Complications (EDC) cohort study

Clinical Epigenetics(2023)10.1186/s13148-023-01539-0

N/A

0DataRank · unranked

5 citations

Josyf C. Mychaleckyj, Suna Önengüt-Gümüşcü, Eleanor Feingold, Trevor J. Orchard, Tina Costacou +1 more

The effects of mosaicism on biological and clinical markers of Alzheimer's disease in adults with Down syndrome

EBioMedicine(2024)10.1016/j.ebiom.2024.105433

N/A

0DataRank · unranked

6 citations

Lam‐Ha T. Dang, Alice Lee, Sharon J. Krinsky‐McHale, Deborah Pang, Lisa Melilli +72 more

Search for the elusive haplotype of the APOE polymorphism associated with Alzheimer’s disease

Research Square(2024)10.21203/rs.3.rs-4902566/v1

N/A

0DataRank · unranked

0 citations

Elizabeth Lawrence, Narges Zafari, Kang-Hsien Fan, Ruyu Shi, Muhammad Aslam +6 more

Correlating hippocampal and amygdala volumes with neuropathological burden in Down syndrome and Alzheimer’s disease and related neurodegenerative pathologies using 7T postmortem MRI

Journal of Neuropathology & Experimental Neurology(2025)10.1093/jnen/nlaf010

N/A

0DataRank · unranked

6 citations

Jinghang Li, Jacob Berardinelli, Hecheng Jin, Tales Santini, Jaehoon Noh +69 more

Sex‐stratified genome‐wide meta‐analysis identifies novel loci for cognitive decline in older adults

Alzheimer s & Dementia(2025)10.1002/alz.14461

N/A

0DataRank · unranked

2 citations

Kang‐Hsien Fan, Beth E. Snitz, Mary Ganguli, Steven T. DeKosky, Oscar L. Lopez +3 more

Search for the elusive haplotype of the APOE polymorphism associated with Alzheimer’s disease

Scientific Reports(2025)10.1038/s41598-025-01263-0

N/A

0DataRank · unranked

1 citations

Kang-Hsien Fan, Elizabeth Lawrence, Narges Zafari, Ruyu Shi, Muhammad Aslam +6 more

APOE Genotype-Stratified Meta-Analysis of Cognitive Decline Reveals Novel Loci for Language and Global Cognitive Function in Older Adults

International Journal of Molecular Sciences(2025)10.3390/ijms26146940

N/A

0DataRank · unranked

1 citations

Kang-Hsien Fan, Beth E. Snitz, Mary Ganguli, Steven T. DeKosky, Oscar L. Lopez +3 more

Inferring chromosome segregation error stage and crossover in trisomic disorders with application to Down syndrome

Nature Communications(2025)10.1038/s41467-025-61413-w

N/A

0DataRank · unranked

0 citations

Wenjian Yang, Gang Wu, Ti‐Cheng Chang, Zhongshan Cheng, Meenakshi Devidas +17 more

Genome‐wide association analyses identify candidate loci for amyloid imaging and plasma biomarkers in adults with Down syndrome

Alzheimer s & Dementia(2025)10.1002/alz.70358

N/A

0DataRank · unranked

0 citations

Lam‐Ha T. Dang, Ruyu Shi, Kang-Hsien Fan, Asma Naseer Cheema, Laura Xicota +16 more

Haploinsufficiency of GRHL2 is associated with orofacial clefting in humans

Human Molecular Genetics(2025)10.1093/hmg/ddaf163

N/A

0DataRank · unranked

0 citations

Cinderella Yang, Alba Sanchis-Juan, Katherine Singleton, Terri H. Beaty, Florian Erger +16 more

Genome-wide analysis identifies novel loci influencing plasma apolipoprotein E concentration and Alzheimer’s disease risk

Molecular Psychiatry(2023)10.1038/s41380-023-02170-4

N/A

0DataRank · unranked

38 citations

Kang-Hsien Fan, Elizabeth Lawrence, Margaret A Bedison, Beth E. Snitz, Steven T. DeKosky +4 more

A Rare Duplication on Chromosome 16p11.2 Is Identified in Patients with Psychosis in Alzheimer's Disease

UNC Libraries(2020)10.17615/14zm-t044

N/A

0DataRank · unranked

2 citations

Robert A. Sweet, M. Michael Barmada, Oscar L. López, M. Ilyas Kamboh, Eleanor Feingold +3 more

Insights into the genetic architecture of the human face

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.12.090555

N/A

0DataRank · unranked

10 citations

Karlijne Indencleef, Sahin Naqvi, Ryan J. Eller, Jasmien Roosenboom, Myoung Keun Lee +17 more

Biological Pathways of Long‐Term Visit‐to‐Visit Blood Pressure Variability in the American Population: Cardiovascular Health Study and Women’s Health Initiatives

BioMed Research International(2020)10.1155/2020/3841945

N/A

0DataRank · unranked

0 citations

Mohammed S. Orloff, Robert R. Delongchamp, Yan Wang, Eleanor Feingold, Susan Thapa +6 more

Coding de novo mutations identified by WGS reveal novel orofacial cleft genes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.01.019927

N/A

0DataRank · unranked

0 citations

Kimberly Diaz Perez, Miranda Sun, Samantha Ho, Pankaj Chopra, Nandita Mukhopadhyay +22 more

Genome-wide interaction study implicates VGLL2 and alcohol exposure and PRL and smoking in orofacial cleft risk

medRxiv(2020)10.1101/2020.10.26.20219980

N/A

0DataRank · unranked

0 citations

John R. Shaffer, Fred Deleyiannis, Jacqueline T. Hecht, George L. Wehby, Kaare Christensen +5 more

Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions

Frontiers in Cell and Developmental Biology(2021)10.3389/fcell.2021.621482

N/A

0DataRank · unranked

33 citations

Eleanor Feingold, Lina Moreno‐Uribe, George L. Wehby, Luz Consuelo Valencia‐Ramirez, Claudia P. Restrepo Muñeton +16 more

The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100025

N/A

0DataRank · unranked

24 citations

Daniel Chang, Myoung Keun Lee, John R. Shaffer, Karlijne Indencleef, Michael P. Epstein +10 more

Analyses stratified by maternal age and recombination further characterize genes associated with maternal nondisjunction of chromosome 21

Prenatal Diagnosis(2021)10.1002/pd.5919

N/A

0DataRank · unranked

8 citations

Stephanie L. Sherman, Eleanor Feingold, Jonathan M. Chernus

FAT4 Identified as a Potential Modifier of Orofacial Cleft Laterality

medRxiv(2021)10.1101/2021.03.16.21253740

N/A

0DataRank · unranked

0 citations

Daniel Chang, Miranda Sun, Michael P. Epstein, Jeffrey C. Murray, Eleanor Feingold +7 more