Emily K. Mis

2.4k total citations · 2 hit papers
24 papers, 1.3k citations indexed

About

Emily K. Mis is a scholar working on Molecular Biology, Genetics and Aging. According to data from OpenAlex, Emily K. Mis has authored 24 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 11 papers in Genetics and 4 papers in Aging. Recurrent topics in Emily K. Mis's work include CRISPR and Genetic Engineering (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genetics, Aging, and Longevity in Model Organisms (4 papers). Emily K. Mis is often cited by papers focused on CRISPR and Genetic Engineering (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genetics, Aging, and Longevity in Model Organisms (4 papers). Emily K. Mis collaborates with scholars based in United States, Canada and Pakistan. Emily K. Mis's co-authors include Mustafa K. Khokha, Charles E. Vejnar, Antonio J. Giráldez, Miguel A. Moreno-Mateos, Juan Pablo Fernández, Jean-Denis Beaudoin, Maura Lane, Romain Rouet, Jennifer A. Doudna and Engin Deniz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Emily K. Mis

20 papers receiving 1.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

CRISPRscan: designing highly efficient sgRNAs for CRISPR-Cas9 targeting in vivo

2015 880 citations Miguel A. Moreno-Mateos, Charles E. Vejnar et al. Nature Methods profile →
CRISPR-Cpf1 mediates efficient homology-directed repair and temperature-controlled genome editing

2017 206 citations Miguel A. Moreno-Mateos, Juan Pablo Fernández et al. Nature Communications profile →

Peers

Countries citing papers authored by Emily K. Mis

Since Specialization

Citations

This map shows the geographic impact of Emily K. Mis's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Emily K. Mis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emily K. Mis more than expected).

Fields of papers citing papers by Emily K. Mis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emily K. Mis. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Emily K. Mis. The network helps show where Emily K. Mis may publish in the future.

Co-authorship network of co-authors of Emily K. Mis

This figure shows the co-authorship network connecting the top 25 collaborators of Emily K. Mis. A scholar is included among the top collaborators of Emily K. Mis based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Emily K. Mis. Emily K. Mis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Biallelic variants in the conserved ribosomal protein chaperone gene PDCD2 are associated with hydrops fetalis and early pregnancy loss 2025 ·Proceedings of the National Academy of Sciences ·(unknown), (unknown), Emily K. Mis, (unknown), Malik Alawi, Weizhen Ji, (unknown), (unknown), François Bachand, Saquib A. Lakhani	0
2	Exome sequencing reveals genetic heterogeneity in consanguineous Pakistani families with neurodevelopmental and neuromuscular disorders 2024 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·(unknown), Weizhen Ji, (unknown), Cynthia Zerillo, Monica Konstantino, Emily K. Mis, (unknown), Mustafa K. Khokha, Saquib A. Lakhani, Sajid Malik	0
3	Sequence variants in DLX5 , HOXD13 and 445 kb‐microduplication surrounding BTRC cause split‐hand/foot malformation in three different families 2023 ·Clinical Genetics ·Abdullah Abdullah, Shabir Hussain, Weizhen Ji, (unknown), Emily K. Mis, (unknown), (unknown), Muhammad Hassan Raza, (unknown), Imran Ullah, Mustafa K. Khokha, Saquib A. Lakhani, Wasim Ahmad	0
4	Sequence variants in different genes underlying Bardet-Biedl syndrome in four consanguineous families 2023 ·Molecular Biology Reports ·Amjad Ali, Abdullah Abdullah, Muhammad Bilal, Emily K. Mis, Saquib A. Lakhani, Wasim Ahmad, Imran Ullah	0
5	A retrospective cohort analysis of the Yale pediatric genomics discovery program 2022 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), E. Vincent S. Faustino, Weizhen Ji, Emily K. Mis, Monica Konstantino, Cynthia Zerillo, Yong‐hui Jiang, (unknown), A. Bale, Hui Zhang, (unknown), James McGrath, (unknown), Nina N. Brodsky, C. Lucas, Richard W. Pierce, Engin Deniz, Mustafa K. Khokha, Saquib A. Lakhani	1
6	Microinjection of Xenopus tropicalis Embryos 2021 ·Cold Spring Harbor Protocols ·Maura Lane, Emily K. Mis, Mustafa K. Khokha	8
7	Xenopus Tadpole Craniocardiac Imaging Using Optical Coherence Tomography 2021 ·Cold Spring Harbor Protocols ·Engin Deniz, Emily K. Mis, Maura Lane, Mustafa K. Khokha	3
8	Familial Dilated Cardiomyopathy Associated With a Novel Combination of Compound Heterozygous TNNC1 Variants 2020 ·Frontiers in Physiology ·Maicon Landim-Vieira, (unknown), Weizhen Ji, Emily K. Mis, (unknown), (unknown), (unknown), E. Kevin Hall, (unknown), Mustafa K. Khokha, Engin Deniz, P. Bryant Chase, Saquib A. Lakhani, José R. Pinto	21
9	Disrupted ER membrane protein complex–mediated topogenesis drives congenital neural crest defects 2020 ·Journal of Clinical Investigation ·Jonathan Marquez, (unknown), Rebekah M. Charney, Maneeshi S. Prasad, Woong Y. Hwang, Emily K. Mis, Martín I. García‐Castro, Mustafa K. Khokha	25
10	DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes 2020 ·Journal of Medical Genetics ·Jonathan Marquez, Nina Mann, (unknown), Engin Deniz, Weizhen Ji, Monica Konstantino, Emily K. Mis, Charu Deshpande, (unknown), (unknown), Hannah Hugo, Eugen Widmeier, Martin Konrad, Velibor Tasić, Raffaella Morotti, Júlia Baptista, Sian Ellard, Saquib A. Lakhani, Friedhelm Hildebrandt, Mustafa K. Khokha	10
11	RPSA, a candidate gene for isolated congenital asplenia, is required for pre-rRNA processing and spleen formation in Xenopus 2018 ·Development ·John N. Griffin, Samuel B. Sondalle, Andrew Robson, Emily K. Mis, (unknown), Saurabh S. Kulkarni, Engin Deniz, Susan J. Baserga, Mustafa K. Khokha	15
12	CRISPR/Cas9 F0 Screening of Congenital Heart Disease Genes in Xenopus tropicalis 2018 ·Methods in molecular biology ·Engin Deniz, Emily K. Mis, Maura Lane, Mustafa K. Khokha	20
13	De novo pathogenic variants in neuronal differentiation factor 2 (NEUROD2) cause a form of early infantile epileptic encephalopathy 2018 ·Journal of Medical Genetics ·(unknown), Emily K. Mis, Kristin Lindstrom, Saadet Mercimek‐Andrews, Weizhen Ji, Megan T. Cho, Jane Juusola, Monica Konstantino, (unknown), Mustafa K. Khokha, Saquib A. Lakhani	25
14	CRISPR-Cpf1 mediates efficient homology-directed repair and temperature-controlled genome editing breakdown → 2017 ·Nature Communications ·Miguel A. Moreno-Mateos, Juan Pablo Fernández, Romain Rouet, Charles E. Vejnar, Maura Lane, Emily K. Mis, Mustafa K. Khokha, Jennifer A. Doudna, Antonio J. Giráldez	206
15	Visualization and quantification of injury to the ciliated epithelium using quantitative flow imaging and speckle variance optical coherence tomography 2017 ·Scientific Reports ·Ute A. Gamm, (unknown), Emily K. Mis, Mustafa K. Khokha, Michael A. Choma	7
16	Ultrahigh-speed, phase-sensitive full-field interferometric confocal microscopy for quantitative microscale physiology 2016 ·Biomedical Optics Express ·İkbal Şencan, (unknown), (unknown), Emily K. Mis, Mustafa K. Khokha, Hui Cao, Michael A. Choma	2
17	CRISPRscan: designing highly efficient sgRNAs for CRISPR-Cas9 targeting in vivo breakdown → 2015 ·Nature Methods ·Miguel A. Moreno-Mateos, Charles E. Vejnar, Jean-Denis Beaudoin, Juan Pablo Fernández, Emily K. Mis, Mustafa K. Khokha, Antonio J. Giráldez	880
18	Forward genetics defines Xylt1 as a key, conserved regulator of early chondrocyte maturation and skeletal length 2013 ·Developmental Biology ·Emily K. Mis, Karel F. Liem, Yong Kong, Nancy B. Schwartz, Miriam S. Domowicz, Scott D. Weatherbee	47
19	High-throughput fluorescence-based isolation of live C. elegans larvae 2012 ·Nature Protocols ·Anita Fernandez, Bastiaan O. R. Bargmann, Emily K. Mis, Mark L. Edgley, Kenneth D. Birnbaum, Fabio Piano	17
20	Using forward genetics to advance our understanding of mouse limb development 2011 ·Developmental Biology ·(unknown), (unknown), Emily K. Mis, Scott D. Weatherbee	1

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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