Mustafa K. Khokha

Biochemistry, Genetics and Molecular BiologyMedicine

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 4%percentile

0.683Author 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.

Conserved chromatin and repetitive patterns reveal slow genome evolution in frogs

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.18.464293

Top 38%

0.507DataRank

Top 38%11 citations

Austin B. Mudd, Sofía Medina-Ruiz, Therese Mitros, Owen K. Smith, Kelly E. Miller +30 more

Papers

Driven by 37 papers — median percentile 48. Top paper: “Conserved chromatin and repetitive patterns reveal slow genome evolution in frogs”.

Conserved chromatin and repetitive patterns reveal slow genome evolution in frogs

Nature Communications(2024)10.1038/s41467-023-43012-9

N/A

0.808DataRank · unranked

43 citations

Austin B. Mudd, Sofía Medina-Ruiz, Therese Mitros, Owen K. Smith, Kelly E. Miller +30 more

Conserved chromatin and repetitive patterns reveal slow genome evolution in frogs

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.18.464293

Top 38%

0.507DataRank

Top 38%11 citations

Austin B. Mudd, Sofía Medina-Ruiz, Therese Mitros, Owen K. Smith, Kelly E. Miller +30 more

A retrospective cohort analysis of the Yale pediatric genomics discovery program

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62918

Top 67%

0.176DataRank

Top 67%2 citations

Lauren Jeffries, E. Vincent S. Faustino, Weizhen Ji, Emily K. Mis, Monica Konstantino +15 more

Challenges and opportunities at the interface of birth defects, human genetics and developmental biology

Development(2020)10.1242/dev.197871

N/A

0DataRank · unranked

15 citations

Karen Liu, John B. Wallingford, Mustafa K. Khokha

A nonsense variant in Rap Guanine Nucleotide Exchange Factor 5 (RAPGEF5) is associated with equine familial isolated hypoparathyroidism in Thoroughbred foals

PLoS Genetics(2020)10.1371/journal.pgen.1009028

N/A

0DataRank · unranked

11 citations

K. Gary Magdesian, Sophia Fagan, Nathan M. Slovis, Daniela Luethy, Laura H. Javsicas +10 more

Recessive Mutations in SYNPO2 as a Candidate of Monogenic Nephrotic Syndrome

Kidney International Reports(2020)10.1016/j.ekir.2020.10.040

N/A

0DataRank · unranked

11 citations

Ronen Schneider, Peter F. M. van der Ven, Marvin Aßent, Keerthika Lohanadan, Verena Klämbt +24 more

Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

Human Molecular Genetics(2020)10.1093/hmg/ddaa050

N/A

0DataRank · unranked

42 citations

Athina Ververi, Ana Beleza‐Meireles, Weizhen Ji, Emily K. Mis, Quinten Patterson +25 more

Disrupted ER membrane protein complex–mediated topogenesis drives congenital neural crest defects

Journal of Clinical Investigation(2020)10.1172/jci129308

N/A

0DataRank · unranked

38 citations

June Criscione, Rebekah M. Charney, Maneeshi S. Prasad, Woong Y. Hwang, Emily K. Mis +3 more

DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.11.008

N/A

0DataRank · unranked

34 citations

Konstantin Deutsch, Gregory J. Hoeprich, Jonathan Marquez, Tobias Hermle, Daniela A. Braun +28 more

Nucleoporin NUP205 plays a critical role in cilia and congenital disease

Developmental Biology(2020)10.1016/j.ydbio.2020.10.001

N/A

0DataRank · unranked

29 citations

Dipankan Bhattacharya, C. Patrick Lusk, Mustafa K. Khokha, Jonathan Marquez

A convergent molecular network underlying autism and congenital heart disease

Cell Systems(2021)10.1016/j.cels.2021.07.009

N/A

0DataRank · unranked

45 citations

Helen Rankin Willsey, Yuxiao Xu, Mei Yuan, Jeanselle Dea, Sheng Wang +8 more

Mechanical stretch scales centriole number to apical area via Piezo1 in multiciliated cells

eLife(2021)10.7554/elife.66076

N/A

0DataRank · unranked

41 citations

Jonathan Marquez, Priya Date, Rosa Ventrella, Brian J. Mitchell, Mustafa K. Khokha +1 more

Expansion of NEUROD2 phenotypes to include developmental delay without seizures

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62064

N/A

0DataRank · unranked

11 citations

Annalisa G. Sega, Rebecca Signer, Tracy Cartwright, Weizhen Ji, Julián A. Martínez-Agosto +12 more

Kap-β2/Transportin mediates β-catenin nuclear transport in Wnt signaling

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.22.445277

N/A

0DataRank · unranked

0 citations

Valentyna Kostiuk, Delfina P. González, C. Patrick Lusk, Mustafa K. Khokha, Woong Y. Hwang

Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR

Nature Communications(2022)10.1038/s41467-022-34363-w

N/A

0DataRank · unranked

38 citations

Valentyna Kostiuk, Jie Zhu, Guerra Mc, Leonid Tyan, Woong Y. Hwang +7 more

Kap-β2/Transportin mediates β-catenin nuclear transport in Wnt signaling

eLife(2022)10.7554/elife.70495

N/A

0DataRank · unranked

17 citations

Valentyna Kostiuk, Delfina P. González, C. Patrick Lusk, Mustafa K. Khokha, Woong Y. Hwang

Mink1 regulates spemann organizer cell fate in the xenopus gastrula via Hmga2

Developmental Biology(2022)10.1016/j.ydbio.2022.11.010

N/A

0DataRank · unranked

4 citations

Mustafa K. Khokha, Vaughn Colleluori

Expanding EMC Foldopathies: Topogenesis Deficits Alter the Neural Crest

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.05.16.492013

N/A

0DataRank · unranked

1 citations

Mustafa K. Khokha, Jonathan Marquez

Membrane phosphoinositides and renal epithelial cell polarity determination in the Xenopus pronephros in vivo

The FASEB Journal(2022)10.1096/fasebj.2022.36.s1.r4889

N/A

0DataRank · unranked

0 citations

Vanathy Rajendran, Mustafa K. Khokha, Michael J. Caplan, Giorgia Schena

CFAP45, a heterotaxy and congenital heart disease gene, affects cilia stability

Developmental Biology(2023)10.1016/j.ydbio.2023.04.006

N/A

0DataRank · unranked

27 citations

Mehreen Pasha, María Elena Guerra, Stephen Viviano, Weidong Ji, Monica Konstantino +7 more

Mitochondrial leak metabolism induces the Spemann-Mangold Organizer via Hif-1α in Xenopus

Developmental Cell(2023)10.1016/j.devcel.2023.08.015

N/A

0DataRank · unranked

11 citations

Nelli Mnatsakanyan, Jeet H. Patel, Andrea E. Wills, Amy Shteyman, Peter J. Smith +4 more

Expanding EMC foldopathies: Topogenesis deficits alter the neural crest

genesis(2023)10.1002/dvg.23520

N/A

0DataRank · unranked

3 citations

Faiza Aslam, Mustafa K. Khokha, Jonathan Marquez

AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia

Neurobiology of Disease(2024)10.1016/j.nbd.2024.106537

N/A

0DataRank · unranked

5 citations

Saikat Ghosh, Lassana Cissé, Thomas Coulibaly, Abdoulaye Yalcouyé, George G. Harmison +20 more

The Heterotaxy Gene CCDC11 Is Important for Cytokinesis via RhoA Regulation

Cytoskeleton(2024)10.1002/cm.21952

N/A

0DataRank · unranked

4 citations

Rachel E. Stephenson, Sarah Amalraj, Angelo B. Arrigo, Ewelina Betleja, James J. Moresco +5 more

The dishevelled associated activator of morphogenesis protein 2 (Daam2) regulates neural tube closure

Developmental Dynamics(2024)10.1002/dvdy.720

N/A

0DataRank · unranked

4 citations

Baihao Su, Jonathan Marquez, Mustafa K. Khokha, Raymond Habas, Kaushik Nama

Genetic profile of progressive myoclonic epilepsy in Mali reveals novel findings

Frontiers in Neurology(2024)10.3389/fneur.2024.1455467

N/A

0DataRank · unranked

1 citations

Salia Bamba, Seybou Hassane Diallo, Weizhen Ji, M Dembélé, Abdoulaye Yalcouyé +18 more

CALHM2 is a mitochondrial protein import channel that regulates fatty acid metabolism

Research Square(2024)10.21203/rs.3.rs-4985689/v1

N/A

0DataRank · unranked

0 citations

Nelli Mnatsakanyan, Félix Rivera-Molina, Andrew Robson, Alexandra MacColl Garfinkel, Amrendra Kumar +10 more

A microscopy-based CRISPR screening platform enables organellar functional genomics and illuminates ciliary biology

Developmental Cell(2025)10.1016/j.devcel.2025.10.015

N/A

0DataRank · unranked

1 citations

İrem Sude Atiş, Stéfany L L Empke, Mustafa K. Khokha, David K. Breslow, Jingbo Sun

Nup107 contributes to the maternal-to-zygotic transition by preventing the premature nuclear export of pri-miR427

Development(2025)10.1242/dev.202865

N/A

0DataRank · unranked

2 citations

Rakib Kabir, Kaitlin Levangie, Stefany Lucas Lopes Empke, Kimberly J. Morgan, Nick Owens +3 more

A novel variant in ARSA causes a rare phenotype of infantile metachromatic leukodystrophy in a Malian family

Neurogenetics(2025)10.1007/s10048-025-00814-x

N/A

0DataRank · unranked

2 citations

Abdoulaye Arama, Abdoulaye Yalcouyé, Mohamed Albakaye, Ji Weizhen, Salia Bamba +10 more

A yeast model reveals the SMAD3 nuclear import mechanism

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.07.09.663975

N/A

0DataRank · unranked

0 citations

Morgan Emokpae, C. Patrick Lusk, Mustafa K. Khokha, Delfina P. González

TMBIM4 affects left-right patterning via pluripotency exit during gastrulation

Developmental Biology(2025)10.1016/j.ydbio.2025.07.018

N/A

0DataRank · unranked

0 citations

Valentyna Kostiuk, Leonid Tyan, Emily K. Mis, David Zenisek, Mustafa K. Khokha +1 more

Trio exome analysis is a valuable tool for genetic diagnosis of epilepsy in Mali

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103449

N/A

0DataRank · unranked

0 citations

Lauren Jeffries, Salimata Diarra, Karamoko Nimaga, Amadou Touré, Modibo K. Goita +28 more

De novo damaging variants associated with congenital heart diseases contribute to the connectome

Scientific Reports(2020)10.1038/s41598-020-63928-2

N/A

0DataRank · unranked

60 citations

Dina Ferdman, Joshua A. Copel, Dustin Scheinost, Veronika Shabanova, Martina Brueckner +3 more

Challenges and opportunities for understanding the genetic causes of congenital anomalies

Developmental Biology(2025)10.1016/j.ydbio.2025.12.001

N/A

0DataRank · unranked

0 citations

Ivan P. Moskowitz, Rolf W. Stottmann, Irene E. Zohn, Mustafa K. Khokha, Janina Kueper

Differential turnover of Nup188 controls its levels at centrosomes and role in centriole duplication

The Journal of Cell Biology(2020)10.1083/jcb.201906031

N/A

0DataRank · unranked

17 citations

Karthigeyan Dhanasekeran, Madeleine Chalfant, Ivan Surovstev, Mustafa K. Khokha, C. Patrick Lusk +1 more

Paired Box 9 (PAX9), the RNA polymerase II transcription factor, regulates human ribosome biogenesis and craniofacial development

PLoS Genetics(2020)10.1371/journal.pgen.1008967

N/A

0DataRank · unranked

17 citations

Engin Deniz, Maya M. Overton, Mustafa K. Khokha, Susan J. Baserga, Katherine I. Farley‐Barnes

Mustafa K. Khokha

Indexed papers

Top data-sharing exemplar

Papers