F. Sessions Cole

Also affiliated with Mallinckrodt (United States)

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

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

1.1Author 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.

From karyotypes to precision genomics in 9p deletion and duplication syndromes

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100081

Top 24%

0.827DataRank

Top 24%25 citations

Jeffrey K. Ng, Victoria Tate, Ying‐Chen Claire Hou, Yang Cao, Lucinda Antonacci-Fulton +8 more

Papers

Driven by 51 papers — median percentile 59. Top paper: “From karyotypes to precision genomics in 9p deletion and duplication syndromes”.

From karyotypes to precision genomics in 9p deletion and duplication syndromes

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100081

Top 24%

0.827DataRank

Top 24%25 citations

Jeffrey K. Ng, Victoria Tate, Ying‐Chen Claire Hou, Yang Cao, Lucinda Antonacci-Fulton +8 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

Documentation of acute kidney injury at discharge from the neonatal intensive care unit and role of nephrology consultation

Journal of Perinatology(2022)10.1038/s41372-022-01424-3

N/A

0.514DataRank · unranked

17 citations

Paulomi Chaudhry, Matthew W. Harer, Shina Menon, Andrew M. South, Ashley Chappell +70 more

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

Nature Communications(2025)10.1038/s41467-025-61712-2

N/A

0.269DataRank · unranked

5 citations

Mikhail A. Moldovan, Rebecca Reimers, Daniel Traviglia, Xinyun Li, Danielle Barnum +95 more

Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes

Genome Medicine(2025)10.1186/s13073-025-01563-0

Top 58%

0.269DataRank

Top 58%5 citations

Eleanor I. Sams, Rachel Slaugh, Sandra Crocker, Emily Cordova Hurtado, Sophia Tracy +66 more

The Challenge of Risk Stratification of Infants Born Preterm in the Setting of Competing and Disparate Healthcare Outcomes

The Journal of Pediatrics(2020)10.1016/j.jpeds.2020.04.043

N/A

0DataRank · unranked

11 citations

Christopher McPherson, Zachary A. Vesoulis, B. A. Cohlan, Rakesh Rao, Barbara Warner +2 more

Low hemoglobin levels are independently associated with neonatal acute kidney injury: a report from the AWAKEN Study Group

Pediatric Research(2020)10.1038/s41390-020-0963-x

N/A

0DataRank · unranked

8 citations

David J. Askenazi, Louis Boohaker, Linzi Li, John D. Mahan, Jennifer R. Charlton +62 more

Phenotypic expansion of KMT2D‐related disorder: Beyond Kabuki syndrome

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61518

N/A

0DataRank · unranked

37 citations

Rebecca C. Spillmann, Daniel Wegner, Jennifer Wambach, Frances V. White, Kathleen Sisco +6 more

Precise breakpoint detection in a patient with 9p– syndrome

Molecular Case Studies(2020)10.1101/mcs.a005348

N/A

0DataRank · unranked

12 citations

Eleanor I. Sams, Dustin Baldridge, Milinn Kremitzki, Daniel Wegner, Tina Lindsay +4 more

Patient-specific iPSCs carrying an SFTPC mutation reveal the intrinsic alveolar epithelial dysfunction at the inception of interstitial lung disease

Cell Reports(2021)10.1016/j.celrep.2021.109636

N/A

0DataRank · unranked

112 citations

Scott J. Russo, Anton Petcherski, Evan P. Taddeo, Rebeca Acín‐Pérez, Carlos Villacorta-Martín +22 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

A phase 1/2 open label nonrandomized clinical trial of intravenous 2-hydroxypropyl-β-cyclodextrin for acute liver disease in infants with Niemann-Pick C1

Molecular Genetics and Metabolism Reports(2021)10.1016/j.ymgmr.2021.100772

N/A

0DataRank · unranked

12 citations

Laura Linneman, Sofia E. Luna, Barbara B. Warner, Yumirle P. Turmelle, Sakil Kulkarni +8 more

Whole exome sequencing and functional characterization increase diagnostic yield in siblings with a 46, XY difference of sexual development (DSD)

The Journal of Steroid Biochemistry and Molecular Biology(2021)10.1016/j.jsbmb.2021.105908

N/A

0DataRank · unranked

1 citations

Daniel Wegner, Sarah Gale, Ping Yang, Abby Hollander, Lori St. Dennis-Feezle +5 more

De novo variants in the PSMC3 proteasome AAA-ATPase subunit gene cause neurodevelopmental disorders associated with type I interferonopathies

medRxiv(2021)10.1101/2021.12.07.21266342

N/A

0DataRank · unranked

3 citations

Sébastien Küry, Victoria Most, Cory Rosenfelt, Marie‐Pier Scott‐Boyer, Geeske M. van Woerden +67 more

The Role of Genome Sequencing in Neonatal Intensive Care Units

Annual Review of Genomics and Human Genetics(2022)10.1146/annurev-genom-120921-103442

N/A

0DataRank · unranked

92 citations

F. Sessions Cole, Stephen F. Kingsmore

Improving child health through Big Data and data science

Pediatric Research(2022)10.1038/s41390-022-02264-9

N/A

0DataRank · unranked

27 citations

Ameena Husain, F. Sessions Cole, Zachary A. Vesoulis

Measuring BMI change among children and adolescents

Pediatric Obesity(2022)10.1111/ijpo.12889

N/A

0DataRank · unranked

24 citations

Amy J. Goodwin Davies, Thao-Ly T. Phan, F. Sessions Cole, Nathan M. Pajor, Suchitra Rao +6 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

First Steps toward Personalized Therapies for ABCA3 Deficiency

American Journal of Respiratory Cell and Molecular Biology(2022)10.1165/rcmb.2021-0405ed

N/A

0DataRank · unranked

3 citations

Lawrence M. Nogee, F. Sessions Cole, Jennifer Wambach

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

PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production

Science Translational Medicine(2023)10.1126/scitranslmed.abo3189

N/A

0DataRank · unranked

36 citations

Sébastien Küry, Victoria Most, Cory Rosenfelt, Marie‐Pier Scott‐Boyer, Geeske M. van Woerden +69 more

Neonatal nephrotoxic medication exposure and early acute kidney injury: results from the AWAKEN study

Journal of Perinatology(2023)10.1038/s41372-023-01684-7

N/A

0DataRank · unranked

19 citations

Jennifer R. Charlton, Meagan Briley, David T. Selewski, Katja M. Gist, Mina Hanna +66 more

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

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

0DataRank · unranked

6 citations

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

Case report: ocular manifestations of a gain-of-function mutation in CLCN6 , a newly diagnosed disease

Ophthalmic Genetics(2023)10.1080/13816810.2023.2291683

N/A

0DataRank · unranked

0 citations

Sameera Nadimpalli, Sudhi P. Kurup, F. Sessions Cole, Russell Huang, Kathleen Sisco +7 more

Large-scale mutational analysis identifies UNC93B1 variants that drive TLR-mediated autoimmunity in mice and humans

The Journal of Experimental Medicine(2024)10.1084/jem.20232005

N/A

0DataRank · unranked

37 citations

Julian A. Yano, John Huizar, Leianna C. Slayden, Madeleine A. Weiss, Elizabeth A Turcotte +93 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

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

The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

Genetics in Medicine(2024)10.1016/j.gim.2024.101203

N/A

0DataRank · unranked

0 citations

Laura Findley, Weihong Ni, Janet S. Sinsheimer, Francesca Cole, Cecilia Esteves +94 more

Recurrent p.H119Y variant in MAP2K1 expands the phenotypic spectrum of MAP2K1‐related RASopathy

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63854

N/A

0DataRank · unranked

0 citations

Daniel Wegner, Jennifer Wambach, Kathleen Sisco, Stephen Stone, Jonathan H. Sheehan +6 more

De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies

Genetics in Medicine(2025)10.1016/j.gim.2025.101369

N/A

0DataRank · unranked

4 citations

Lindsay C. Burrage, Sharayu Jangam, Jill A. Rosenfeld, Sandra von Hardenberg, Anke K. Bergmann +92 more

Enriched phenotypes in rare variant carriers suggest pathogenic mechanisms in rare disease patients

BioData Mining(2025)10.1186/s13040-024-00418-5

N/A

0DataRank · unranked

1 citations

Undiagnosed Diseases Network, Maria T. Acosta, David R. Adams, Ben Afzali, Ali Al-Beshri +95 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

0DataRank · unranked

70 citations

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

Lentiviral-mediated gene complementation rescues pathogenic ABCA3 variants

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.08.29.673150

N/A

0DataRank · unranked

0 citations

S. Lamer, Ping Yang, Daniel J. Wegner, Frances V. White, F. Sessions Cole +8 more

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

Functional characterization of four ATP‐binding cassette transporter A3 gene (ABCA3) variants

Human Mutation(2020)10.1002/humu.24014

N/A

0DataRank · unranked

20 citations

Ping Yang, Daniel Wegner, Hillary B. Heins, Cliff J. Luke, Fuhai Li +5 more

Discovery of a novel CHD7 CHARGE syndrome variant by integrated omics analyses

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61962

N/A

0DataRank · unranked

10 citations

Daniel Wegner, Alexander J. Paul, Marcia Willing, Kathleen Sisco, Matthew L. Tedder +6 more

Digenic Variants in the FGF21 Signaling Pathway Associated with Severe Insulin Resistance and Pseudoacromegaly

Journal of the Endocrine Society(2020)10.1210/jendso/bvaa138

N/A

0DataRank · unranked

12 citations

Daniel Wegner, Jennifer Wambach, F. Sessions Cole, Fumihiko Urano, David M. Ornitz +1 more

F. Sessions Cole

Indexed papers

Top data-sharing exemplar

Papers