Kiely N. James

2.1k citations

20 papers · 360 indexed · h-index 12

Cellular and Molecular Neuroscience
- Photoreceptor and optogenetics research 3
- Neuroscience and Neuropharmacology Research 2
Genetics
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 3
Molecular Biology
- Retinal Development and Disorders 3
- Hedgehog Signaling Pathway Studies 2
Cell Biology
Cancer Research
Pathology and Forensic Medicine
- Genetic factors in colorectal cancer 2

Co-authors: David A. Feldheim Neal Sweeney Martin W. Breuss Shimul Chowdhury Michael Farzan Yan Cao Sheila A. Baker Naomi Kamasawa
Cited by: Cellular and Molecular Neuroscience Genetics Molecular Biology
Journals: Cell (2 papers)Neuron (1 paper)The Journal of Comparative Neurology (1 paper)
Partner nations: United States Austria Belgium

In The Last Decade

Kiely N. James

20 papers receiving 356 citations

Peers

Countries citing papers authored by Kiely N. James

Since Specialization

Citations

This map shows the geographic impact of Kiely N. James'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 Kiely N. James with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kiely N. James more than expected).

Fields of papers citing papers by Kiely N. James

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kiely N. James. 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 Kiely N. James. The network helps show where Kiely N. James may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Kiely N. James, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Kiely N. James Line = papers co-authored together Kiely N. James links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Functional sensory circuits built from neurons of two species Cell ·Benjamin T. Throesch,Muhammad Khadeesh bin Imtiaz,Rodrigo Muñoz-Castañeda,Masahiro Sakurai,Andrea L. Hartzell,Kiely N. James,Alberto R. Rodriguez,Greg Martin,Giordano Lippi,Sergey Kupriyanov,Zhuhao Wu,Pavel Osten,Juan Carlos Izpisúa Belmonte,Jun Wu,Kristin K. Baldwin	2024	8
2	Novel variants inTECRLleading to catecholaminergic polymorphic ventricular tachycardia Life Science Alliance ·Douglas H. Jones,J. Härtung,Elizabeth Lasalle,Alejandro Borquez,Viridiana Murillo,Lucia Guidugli,Kiely N. James,Stephen F. Kingsmore,Nicole G. Coufal	2024	2
3	Genome sequencing detects a wide range of clinically relevant copy-number variants and other genomic alterations Genetics in Medicine ·Kiely N. James,Shimul Chowdhury,Yan Ding,Serge Batalov,Kelly Watkins,Yong Hyun Kwon,Lucitia Van Der Kraan,Katarzyna A. Ellsworth,Stephen F. Kingsmore,Lucia Guidugli	2023	1
4	Artificial Intelligence in the Genetic Diagnosis of Rare Disease Clinics in Laboratory Medicine ·Kiely N. James,Sujal Phadke,Terence C. Wong,Shimul Chowdhury	2023	3
5	Hemimegalencephaly and intractable seizures associated with the NPRL3 gene variant in a newborn: A case report American Journal of Medical Genetics Part A ·Indira Chandrasekar,Anne Tourney,Kamela Loo,Jason Carmichael,Kiely N. James,Katarzyna A. Ellsworth,David Dimmock,Maries Joseph	2021	12
6	Developmental and temporal characteristics of clonal sperm mosaicism Cell ·Xiaoxu Yang,Martin W. Breuss,Xin Xu,Danny Antaki,Kiely N. James,Valentina Stanley,Laurel Ball,Renee D. George,Sara A. Wirth,Beibei Cao,An Nguyen,Jennifer McEvoy‐Venneri,Guoliang Chai,Shareef Nahas,Lucitia Van Der Kraan,Yan Ding,Jonathan Sebat,Joseph G. Gleeson	2021	26
7	Expanding the genotypic spectrum of ACTG2-related visceral myopathy Molecular Case Studies ·Kiely N. James,Megan Lau,Katayoon Shayan,Jerica Lenberg,Rebecca Mardach,Romeo C. Ignacio,Jonathan Halbach,Lillian Choi,Soma Kumar,Katarzyna A. Ellsworth	2021	4
8	Rapid whole-genome sequencing identifies a homozygous novel variant, His540Arg, in HSD17B4 resulting in D-bifunctional protein deficiency disorder diagnosis Molecular Case Studies ·Lane Savage,Stacie D. Adams,Kiely N. James,Shimul Chowdhury,Surender Rajasekaran,Jeremy W. Prokop,Caleb Bupp	2020	7
9	Clinician-centric diagnosis of rare genetic diseases: performance of a gene pertinence metric in decision support for clinicians Orphanet Journal of Rare Diseases ·Michael M. Segal,Renee D. George,Peter Waltman,Ayman W. El‐Hattab,Kiely N. James,Valentina Stanley,Joseph G. Gleeson	2020	5
10	Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnoses npj Genomic Medicine ·Kiely N. James,Michelle M. Clark,Brandon Camp,Cyrielle Kint,Peter Schols,Serge Batalov,Benjamin Briggs,Narayanan Veeraraghavan,Shimul Chowdhury,Stephen F. Kingsmore	2020	32
11	mTOR pathway somatic variants and the molecular pathogenesis of hemimegalencephaly Epilepsia Open ·Camila Araújo Bernardino Garcia,Simone C. S. Carvalho,Xiaoxu Yang,Laurel Ball,Renee D. George,Kiely N. James,Valentina Stanley,Martin W. Breuss,Úrsula Thomé,Marcelo Volpon Santos,Fabiano Pinto Saggioro,Luciano Neder Serafini,Wilson A. Silva,Joseph G. Gleeson,Hélio Rubens Machado	2020	19
12	Mortality in a neonate with molybdenum cofactor deficiency illustrates the need for a comprehensive rapid precision medicine system Molecular Case Studies ·Stephen F. Kingsmore,Nanda Ramchandar,Kiely N. James,Anna‐Kaisa Niemi,Annette Feigenbaum,Yan Ding,Wendy Benson,Charlotte A. Hobbs,Shareef Nahas,Shimul Chowdhury,David Dimmock	2020	12
13	Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers Molecular Genetics & Genomic Medicine ·Job A.J. Verdonschot,Emma Robinson,Kiely N. James,Mohamed W. Mohamed,Godelieve R.F. Claes,Kari Casas,Els K. Vanhoutte,Mark R. Hazebroek,Gabriel Kringlen,M. Pasierb,Arthur van den Wijngaard,Jan F. C. Glatz,Stéphane Heymans,Ingrid P.C. Krapels,Shareef Nahas,Han G. Brunner,Radek Szklarczyk	2019	12
14	Novel Factor XIII variant identified through whole-genome sequencing in a child with intracranial hemorrhage Molecular Case Studies ·Benjamin Briggs,Kiely N. James,Shimul Chowdhury,Courtney D. Thornburg,Lauge Farnaes,David Dimmock,Stephen F. Kingsmore,(unknown)	2018	6
15	Mutations in LNPK, Encoding the Endoplasmic Reticulum Junction Stabilizer Lunapark, Cause a Recessive Neurodevelopmental Syndrome The American Journal of Human Genetics ·Martin W. Breuss,An Nguyen,Qiong Song,Thai B. Nguyen,Valentina Stanley,Kiely N. James,Damir Musaev,Guoliang Chai,Sara A. Wirth,Paula Anzenberg,Renee D. George,Anide Johansen,Shaila Ali,Sohaib Muhammad,Tipu Sultan,Maha S. Zaki,Joseph G. Gleeson	2018	22
16	Expression of transcription factors divides retinal ganglion cells into distinct classes The Journal of Comparative Neurology ·Neal Sweeney,Kiely N. James,Andreea Nistorica,Ryan Lorig-Roach,David A. Feldheim	2017	28
17	Uner Tan syndrome caused by a homozygousTUBB2Bmutation affecting microtubule stability Human Molecular Genetics ·Martin W. Breuss,Thai B. Nguyen,Anjana Srivatsan,Ines Leca,Guoling Tian,Tanja Fritz,Andi H. Hansen,Damir Musaev,Jennifer McEvoy‐Venneri,Kiely N. James,Rasim Özgür Rosti,Eric Scott,Üner Tan,Richard D. Kolodner,Nicholas J. Cowan,David A. Keays,Joseph G. Gleeson	2016	11
18	Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly The American Journal of Human Genetics ·Martin W. Breuss,Tipu Sultan,Kiely N. James,Rasim Özgür Rosti,Eric Scott,Damir Musaev,Bansri Furia,André Reis,Heinrich Sticht,Mohammed Al‐Owain,Fowzan S. Alkuraya,Miriam S. Reuter,Rami Abou Jamra,Christopher R. Trotta,Joseph G. Gleeson	2016	44
19	Ephrin‐as are required for the topographic mapping but not laminar choice of physiologically distinct RGC types Developmental Neurobiology ·Neal Sweeney,Kiely N. James,Emily C. Sales,David A. Feldheim	2015	13
20	Mechanism for Selective Synaptic Wiring of Rod Photoreceptors into the Retinal Circuitry and Its Role in Vision Neuron ·Yan Cao,Ignacio Sarria,Katherine E. Fehlhaber,Naomi Kamasawa,Cesare Orlandi,Kiely N. James,Jennifer L. Hazen,Matthew R. Gardner,Michael Farzan,Amy Lee,Sheila A. Baker,Kristin K. Baldwin,Alapakkam P. Sampath,Kirill A. Martemyanov	2015	93

About Kiely N. James

Kiely N. James is a scholar working on Genetics, Cellular and Molecular Neuroscience and Gastroenterology, having authored 20 papers that have together received 360 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Photoreceptor and optogenetics research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Retinal Development and Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Hedgehog Signaling Pathway Studies (2 papers), Neuroscience and Neuropharmacology Research (2 papers) and Genetic factors in colorectal cancer (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (122 citations), Genetics (107 citations) and Molecular Biology (240 citations). Kiely N. James has collaborated with scholars based in United States, Austria and Belgium. Frequent co-authors include David A. Feldheim, Neal Sweeney, Martin W. Breuss, Shimul Chowdhury, Michael Farzan, Yan Cao, Sheila A. Baker, Naomi Kamasawa, Cesare Orlandi and Matthew R. Gardner. Their work appears in journals such as Cell, Neuron and The Journal of Comparative Neurology.

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