Olveen Carrasquillo

Economics, Econometrics and FinanceMedicineHealth ProfessionsPsychology

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 2%percentile

2.2Author 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Communications Biology(2024)10.1038/s42003-023-05708-y

Top 12%

1.7DataRank

Top 12%52 citations

Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi–Ju Chen, Sara E. Kalla +95 more

Papers

Driven by 43 papers — median percentile 75. Top paper: “The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities”.

The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Communications Biology(2024)10.1038/s42003-023-05708-y

Top 12%

1.7DataRank

Top 12%52 citations

Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi–Ju Chen, Sara E. Kalla +95 more

Investigation of hypertension and type 2 diabetes as risk factors for dementia in the All of Us cohort

Scientific Reports(2022)10.1038/s41598-022-23353-z

N/A

1.0DataRank · unranked

27 citations

Priscilla Pemu, Jun Qian, Eric Boerwinkle, Mine Cicek, Cheryl R. Clark +63 more

De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.02.016

N/A

0.639DataRank · unranked

70 citations

Chloe Reuter, Maura Ruzhnikov, Anita E. Beck, Emily Farrow, Lisa Emrick +91 more

Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment

npj Genomic Medicine(2023)10.1038/s41525-022-00343-8

N/A

0.605DataRank · unranked

18 citations

Vikas Bhambhani, Nour Gazzaz, Mariska Davids, Paalini Sathiyaseelan, Ellen F. Macnamara +95 more

Genetic ancestry and population structure in the All of Us Research Program cohort

Nature Communications(2025)10.1038/s41467-025-59351-8

Top 37%

0.518DataRank

Top 37%15 citations

Shashwat Deepali Nagar, Priscilla Pemu, Stephan Züchner, Robert Meller, Alexander Quarshie +50 more

Increasing uptake of evidence-based screening services though a community health worker-delivered multimodality program: study protocol for a randomized pragmatic trial

Trials(2020)10.1186/s13063-020-4213-7

N/A

0.422DataRank · unranked

8 citations

Julia Seay, Vasanti Jhaveri, Timothy Long, Sonjia Kenya, Emmanuel Thomas +5 more

Continuing a search for a diagnosis: the impact of adolescence and family dynamics

Orphanet Journal of Rare Diseases(2023)10.1186/s13023-022-02598-x

N/A

0.292DataRank · unranked

6 citations

Beverly M. Yashar, Undiagnosed Disease Network, Maria T. Acosta, Margaret P Adam, David R. Adams +95 more

Community engagement during COVID: A field report from seven CTSAs

Journal of Clinical and Translational Science(2021)10.1017/cts.2021.785

N/A

0DataRank · unranked

23 citations

Michael D. Kappelman, Rhonda G. Kost, Gia Mudd‐Martin, Jackilen Shannon, Louisa A. Stark +2 more

Hypertension prevalence in the All of Us Research Program among groups traditionally underrepresented in medical research

Scientific Reports(2021)10.1038/s41598-021-92143-w

N/A

0DataRank · unranked

20 citations

Cheryl R. Clark, Guohai Zhou, Nyia L. Noel, Confidence Achilike, Lizette Mendez +95 more

Is Medicine Just a DREAM for DACA Students? DACA Practices and Policies Among U.S. Medical Schools

Journal of Immigrant and Minority Health(2021)10.1007/s10903-021-01211-w

N/A

0DataRank · unranked

8 citations

Olveen Carrasquillo, BreAnne Young, Sonjia Kenya, Sara Carranco

Acceptability and Feasibility of Home-Based Hepatitis B Screening Among Haitian Immigrants

Journal of Immigrant and Minority Health(2021)10.1007/s10903-021-01165-z

N/A

0DataRank · unranked

5 citations

Kristin N Gmunder, Saradjine Batrony, Paul Martin, Erin N. Kobetz, Olveen Carrasquillo +1 more

How Does Black History Help Doctors? Addressing Cultural Competency through Cinemeducation at a Diverse Medical School

Southern Medical Journal(2021)10.14423/smj.0000000000001225

N/A

0DataRank · unranked

1 citations

BreAnne Young, Janielle Taylor, Olveen Carrasquillo, Erin N. Marcus, Joan E. St. Onge +1 more

The microRNA processorDROSHAis a candidate gene for a severe progressive neurological disorder

Human Molecular Genetics(2022)10.1093/hmg/ddac085

N/A

0DataRank · unranked

17 citations

Mümine Şentürk, Kelly Schoch, Amanda L. Minogue, Diego Lopergolo, Chiara Fallerini +95 more

Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome

Brain(2022)10.1093/brain/awac223

N/A

0DataRank · unranked

16 citations

Aloran Mazumder, Daisuke Ogasawara, Rami Abou Jamra, Geneviève Bernard, Enrico Bertini +94 more

A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder

Genetics in Medicine(2022)10.1016/j.gim.2022.03.014

N/A

0DataRank · unranked

16 citations

Kristin Grimsrud, Louise Lanoue, Alena Egense, Brandon Willis, Johanna Hörberg +95 more

Revisiting the Latino Epidemiologic Paradox: an Analysis of Data from the All of Us Research Program

Journal of General Internal Medicine(2022)10.1007/s11606-022-07625-y

N/A

0DataRank · unranked

11 citations

Jacob L. McCauley, Rosario Isasi, Stephan Züchner, Olveen Carrasquillo, Raúl A Montañez-Valverde

A Latent Profile Analysis of COVID-19 Trusted Sources of Information among Racial and Ethnic Minorities in South Florida

Vaccines(2022)10.3390/vaccines10040545

N/A

0DataRank · unranked

8 citations

Eric F. Wagner, Staci Leon Morris, Victor Cueto, Olveen Carrasquillo, Sara C. Charles +4 more

The CTSA Diversity, Equity, Inclusion, and Accessibility (DEIA) Task Force’s recommendations for the CTSA program consortium

Journal of Clinical and Translational Science(2022)10.1017/cts.2022.512

N/A

0DataRank · unranked

6 citations

Maia Hightower, Vanessa Schick, Tung Nguyen, Bertha Hidalgo, Lisa Cacari Stone +6 more

COVID-19, science, vaccines and family in a multi origin Latinx population in South Florida

Frontiers in Public Health(2022)10.3389/fpubh.2022.997449

N/A

0DataRank · unranked

4 citations

Gira J. Ravelo, Pablo Benı́tez, Jennifer Chavez, Nicholas Metheny, María José Baeza Robba +5 more

A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

Genetics in Medicine(2022)10.1016/j.gim.2022.12.001

N/A

0DataRank · unranked

1 citations

Queenie K.‐G. Tan, Chloe Reuter, Kelly Schoch, Jennefer N. Kohler, Devon Bonner +94 more

Bi-allelic variants in INTS11 are associated with a complex neurological disorder

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.012

N/A

0DataRank · unranked

38 citations

Erica L. Macke, Marcello Niceta, Monika Weisz Hubshman, Oguz Kanca, Laura Schultz‐Rogers +95 more

Community-Engaged Research — Essential to Addressing Health Inequities

New England Journal of Medicine(2023)10.1056/nejmp2307774

N/A

0DataRank · unranked

28 citations

Stephania T. Miller, Alan Richmond, Olveen Carrasquillo, Consuelo H. Wilkins

Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

Genetics in Medicine(2023)10.1016/j.gim.2023.100897

N/A

0DataRank · unranked

10 citations

Kelly Schoch, Rebecca Ganetzky, Peter G. Kranz, Neal Sondheimer, M. Louise Markert +92 more

De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.012

N/A

0DataRank · unranked

8 citations

Rossella Venditti, Evangelos A. Theodorou, Lauren C. Briere, Marion Rosello, Alfonsina Tirozzi +94 more

Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care

The Journal of Pediatrics(2023)10.1016/j.jpeds.2023.113537

N/A

0DataRank · unranked

7 citations

Jennifer L. Young, Charis Tang, Kevin Mintz, Sawyer Lucas-Griffin, AudreyStephannie Maghiro +95 more

De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

Genetics in Medicine(2023)10.1016/j.gim.2023.100833

N/A

0DataRank · unranked

6 citations

Jung-Wan Mok, Oguz Kanca, Sharayu Jangam, Cynthia J. Tifft, Ellen F. Macnamara +95 more

Macrocephaly and developmental delay caused by missense variants in RAB5C

Human Molecular Genetics(2023)10.1093/hmg/ddad130

N/A

0DataRank · unranked

4 citations

Weimin Yuan, Federico Tessadori, Wilmer R. Rodriguez-Polanco, Jeremy J. Grubbs, Bo Zhang +94 more

A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2023.12.004

N/A

0DataRank · unranked

14 citations

Sydney L. Michener, Hongling Pan, Hiuling Chan, Jessica M. Pfliger, Jill A. Rosenfeld +95 more

Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

Genetics in Medicine(2024)10.1016/j.gim.2024.101166

N/A

0DataRank · unranked

11 citations

Nicole Legro, Dustin Baldridge, Jimann Shin, Angela Bowman, Berrak Uğur +89 more

Association between SARS-CoV-2 infection and select symptoms and conditions 31 to 150 days after testing among children and adults

BMC Infectious Diseases(2024)10.1186/s12879-024-09076-8

N/A

0DataRank · unranked

9 citations

Alfonso Romieu-Hernandez, Tegan K. Boehmer, Eduardo Azziz‐Baumgartner, Thomas W. Carton, Adi V. Gundlapalli +42 more

De novo variants in DENND5B cause a neurodevelopmental disorder

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.02.001

N/A

0DataRank · unranked

9 citations

Valeria Tomati, Matteo P. Ferla, Mariateresa Lena, Julie S. Cohen, Ali Fatemi +94 more

Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

Genetics in Medicine(2024)10.1016/j.gim.2024.101115

N/A

0DataRank · unranked

6 citations

Lauren C. Briere, Chloe Reuter, Perman Gochyyev, Maria T. Acosta, David R. Adams +94 more

Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

Genetics in Medicine(2024)10.1016/j.gim.2024.101218

N/A

0DataRank · unranked

4 citations

Kristy Jay, Alden Huang, Jijun Wan, Sharayu Jangam, Odelia Chorin +95 more

Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder

Pediatric Neurology(2024)10.1016/j.pediatrneurol.2024.07.010

N/A

0DataRank · unranked

2 citations

Heena Patel, Siddharth Srivastava, Lindsay C. Swanson, Boris Keren, Sandra Whalen +95 more

LUSTR: a new customizable tool for calling genome-wide germline and somatic short tandem repeat variants

BMC Genomics(2024)10.1186/s12864-023-09935-9

N/A

0DataRank · unranked

0 citations

Camilo Toro, David R. Adams, Undiagnosed Diseases Network, Maria T. Acosta, Margaret P Adam +95 more

Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Communications Biology(2024)10.1038/s42003-024-06408-x

N/A

0DataRank · unranked

0 citations

Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi–Ju Chen, Sara E. Kalla +93 more

Cross-sectional analysis of delays in care and interactions with healthcare providers among transgender and gender diverse individuals

Frontiers in Health Services(2025)10.3389/frhs.2025.1685984

N/A

0DataRank · unranked

0 citations

Olveen Carrasquillo, Diana T. Medina Laabes, Vivian Colón‐López, Kasey A. Hill

Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder

Brain(2020)10.1093/brain/awaa204

N/A

0DataRank · unranked

59 citations

Fanny Kortüm, Georg Christoph Korenke, Malik Alawi, René Santer, Mathias Woidy +95 more

Bridging the gap between research, policy, and practice: Lessons learned from academic–public partnerships in the CTSA network

Journal of Clinical and Translational Science(2020)10.1017/cts.2020.23

N/A

0DataRank · unranked

28 citations

Allison Orechwa, Tomás Aragón, Marc S. Atkins, Arleen F. Brown, Jen Brown +18 more

There’s just not enough time: a mixed methods pilot study of hepatitis C virus screening among baby boomers in primary care

BMC Family Practice(2020)10.1186/s12875-020-01327-2

N/A

0DataRank · unranked

9 citations

Julie Rathwell, Kaitlyn M. Gabhart, Jennifer García, Richard G. Roetzheim, Olveen Carrasquillo +3 more

Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

Genetics in Medicine(2021)10.1038/s41436-020-01084-8

N/A

0DataRank · unranked

34 citations

Dustin Baldridge, Matt Velinder, Joel B. Krier, Kimberly LeBlanc, Cecilia Esteves +90 more

Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

Genetics in Medicine(2021)10.1038/s41436-021-01152-7

N/A

0DataRank · unranked

30 citations

Georgi Stoyanov, Florian Erger, Constantine A. Stratakis, Nikolaos Settas, Edra London +95 more

Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

Genetics in Medicine(2021)10.1038/s41436-021-01216-8

N/A

0DataRank · unranked

26 citations

Jennifer B. Phillips, Elizabeth L. Fieg, Sameer S. Bajikar, Judy Peirce, Jeremy Wegner +94 more

Olveen Carrasquillo

Indexed papers

Top data-sharing exemplar

Papers