🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Melissa Wasserstein

Albert Einstein College of Medicine

ORCID: 0000-0003-2031-7817

Also affiliated with Children's Hospital at Montefiore

MedicineBiochemistry, 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 3%percentile
0.930Author 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 →

Top data-sharing exemplar

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

Clinical variants paired with phenotype: A rich resource for brain gene curation

Genetics in Medicine(2023)10.1016/j.gim.2023.101035
Top 35%
0.557DataRank
Top 35%11 citations

Juliann M. Savatt, Taylor I. Bingaman, Molly Good, Alexis Morgan, Caitlin Cooney +37 more

Papers

Driven by 26 papers — median percentile 58. Top paper: “Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients”.

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

Genetics in Medicine(2023)10.1016/j.gim.2023.100880
N/A
0.564DataRank · unranked
42 citations

Priya N. Marathe, Nicole R. Kelly, Katherine E. Bonini, Monisha Sebastin, Jacqueline A. Odgis +22 more

Clinical variants paired with phenotype: A rich resource for brain gene curation

Genetics in Medicine(2023)10.1016/j.gim.2023.101035
Top 35%
0.557DataRank
Top 35%11 citations

Juliann M. Savatt, Taylor I. Bingaman, Molly Good, Alexis Morgan, Caitlin Cooney +37 more

GUÍA: a digital platform to facilitate result disclosure in genetic counseling

Genetics in Medicine(2021)10.1038/s41436-020-01063-z
N/A
0.505DataRank · unranked
28 citations

Jaqueline A. Odgis, Katie M. Gallagher, Jessica Rodriguez, Dana Watnick, Gabrielle Bertier +27 more

Consensus guidelines for the monitoring and management of metachromatic leukodystrophy in the United States

Cytotherapy(2024)10.1016/j.jcyt.2024.03.487
N/A
0.489DataRank · unranked
25 citations

Joshua L. Bonkowsky, Jaap Jan Boelens, Eric J. Mallack, Rebecca C. Ahrens‐Nicklas, John Bernat +27 more

Hope versus reality: Parent expectations of genomic testing

Patient Education and Counseling(2021)10.1016/j.pec.2021.01.030
N/A
0.470DataRank · unranked
22 citations

Siobhan M. Dolan, Dana Watnick, Katie M. Gallagher, Jacqueline A. Odgis, Sabrina A. Suckiel +7 more

When is the best time to screen and evaluate for treatable genetic disorders?: A lifespan perspective

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2023)10.1002/ajmg.c.32036
N/A
0.457DataRank · unranked
20 citations

Michele Caggana, Jennifer L. Cohen, Nina B. Gold, Jill A. Morris, Joseph J. Orsini +3 more

The Brain Gene Registry: a data snapshot

Journal of Neurodevelopmental Disorders(2024)10.1186/s11689-024-09530-3
Top 48%
0.373DataRank
Top 48%11 citations

Levi Kaster, Catherine Sancimino, Siddharth Srivastava, Sophie Molholm, Aditi Gupta +58 more

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

medRxiv(2023)10.1101/2023.03.18.23286992
N/A
0.312DataRank · unranked
7 citations

Priya Marathe, Nicole Kelly, Katherine E. Bonini, Monisha Sebastin, Jacqueline A. Odgis +22 more

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

medRxiv(2020)10.1101/2020.09.02.20186361
N/A
0.104DataRank · unranked
1 citations

Katie M. Gallagher, Sabrina A. Suckiel, Katherine E. Donohue, Michelle A. Ramos, Nicole Kelly +41 more

Physician and informal care use explained by the Pediatric Quality of Life Inventory (PedsQL) in children with suspected genetic disorders

Quality of Life Research(2024)10.1007/s11136-024-03677-1
N/A
0.104DataRank · unranked
1 citations

Nicole Kelly, Ashley Fisher, Samuel F. Hohmann, Noura S. Abul‐Husn, John M. Greally +6 more

Detection of mosaic variants using genome sequencing in a large pediatric cohort

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.63062
N/A
0DataRank · unranked
14 citations

Katie M. Gallagher, Atteeq U. Rehman, Priya Marathe, Katherine E. Bonini, Monisha Sebastin +21 more

Types A and B Niemann‐Pick Disease

PubMed(2022)10.1002/9781119697312.ch13
N/A
0DataRank · unranked
17 citations

Robert J. Desnick, Edward H. Schuchman, Melissa Wasserstein

Plasma lyso-sphingomyelin levels are positively associated with clinical severity in acid sphingomyelinase deficiency

Molecular Genetics and Metabolism Reports(2021)10.1016/j.ymgmr.2021.100780
N/A
0DataRank · unranked
33 citations

Wenyue Zhang, Chunli Yu, Melissa Wasserstein, Margo Sheck Breilyn

The future of newborn screening for lysosomal disorders

Neuroscience Letters(2021)10.1016/j.neulet.2021.136080
N/A
0DataRank · unranked
41 citations

Joseph J. Orsini, Aaron J. Goldenberg, Michele Caggana, Paul A. Levy, Margo Sheck Breilyn +2 more

Free sialic acid storage disorder: Progress and promise

Neuroscience Letters(2021)10.1016/j.neulet.2021.135896
N/A
0DataRank · unranked
45 citations

Mary E. Hackbarth, David R. Adams, Melissa Wasserstein, Marc C. Patterson, Steven U. Walkley +11 more

Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program

Clinical Genetics(2023)10.1111/cge.14365
N/A
0DataRank · unranked
6 citations

Amanda Thomas‐Wilson, Priya N. Marathe, Monisha Sebastin, Jacqueline A. Odgis, Miranda Di Biase +24 more

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.016
N/A
0DataRank · unranked
6 citations

Nicole Kelly, Jacqueline A. Odgis, Katie M. Gallagher, Monisha Sebastin, Katherine E. Bonini +18 more

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

Research Square(2020)10.21203/rs.3.rs-64844/v1
N/A
0DataRank · unranked
0 citations

Katie M. Gallagher, Sabrina A. Suckiel, Katherine E. Donohue, Michelle A. Ramos, Nicole Kelly +41 more

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families

medRxiv(2023)10.1101/2023.07.05.23292193
N/A
0DataRank · unranked
0 citations

Nicole Kelly, Jacqueline A. Odgis, Katie M. Gallagher, Monisha Sebastin, Katherine E. Bonini +18 more

Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program

Genetics in Medicine(2023)10.1016/j.gim.2023.101011
N/A
0DataRank · unranked
0 citations

Nicole Kelly, Ashley Fisher, Samuel F. Hohmann, Monisha Sebastin, Miranda Di Biase +14 more

GenomeDiver: A platform for phenotype-guided medical genomic diagnosis

medRxiv(2020)10.1101/2020.11.22.20236430
N/A
0DataRank · unranked
0 citations

Christian Stolte, Kevin Shi, Faygel Beren, Noura S. Abul‐Husn, Gabrielle Bertier +12 more

GUÍA: a digital platform to facilitate result disclosure in genetic counseling

medRxiv(2020)10.1101/2020.09.14.20194191
N/A
0DataRank · unranked
0 citations

Jaqueline A. Odgis, Katie M. Gallagher, Jessica Rodriguez, Dana Watnick, Gabrielle Bertier +27 more

Employing effective recruitment and retention strategies to engage a diverse pediatric population in genomics research

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.015
N/A
0DataRank · unranked
4 citations

Katherine E. Bonini, Laura Scarimbolo, Nicole Kelly, Beverly J. Insel, Sabrina A. Suckiel +36 more

Patient and providers’ perspectives on using the GUÍA digital tool to enhance genomic results disclosure

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103451
N/A
0DataRank · unranked
1 citations

Sabrina A. Suckiel, Laura Golfinopoulos, Nicole R. Kelly, Katherine E. Bonini, Priya N. Marathe +15 more

Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100321
N/A
0DataRank · unranked
1 citations

Sabrina A. Suckiel, Katherine E. Bonini, Nicole Kelly, Laura Scarimbolo, Beverly J. Insel +22 more

Population-Based Screening of Newborns: Findings From the NBS Expansion Study (Part One)

Frontiers in Genetics(2022)10.3389/fgene.2022.867337
N/A
0DataRank · unranked
21 citations

Kee Chan, Marc S. Williams, Susan A. Berry, Robert J. Currier, Piero Rinaldo +22 more