James Mull

1.4k citations

19 papers · 1.1k indexed · h-index 14

Impact in

Cellular and Molecular Neuroscience top 5%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Neurology top 5%
- Neurological diseases and metabolism

Papers in ⓘ

Cellular and Molecular Neuroscience 15
- Hereditary Neurological Disorders 15
Molecular Biology 11
- RNA Research and Splicing 5
- RNA regulation and disease 5
- Signaling Pathways in Disease 4

Co-authors: Susan A. Slaugenhaupt (16 shared papers)Maire Leyne (14 shared papers)Felicia B. Axelrod (12 shared papers)James F. Gusella (10 shared papers)Sandra Gill (9 shared papers)Channa Maayan (8 shared papers)Math P. Cuajungco (4 shared papers)Anat Blumenfeld (7 shared papers)
Journals: The American Journal of Human Genetics (3 papers)Infection and Immunity (3 papers)Pediatric Research (3 papers)Genomics (3 papers)Gene (1 paper)
Partner nations: United States Israel Saudi Arabia

In The Last Decade

James Mull

19 papers receiving 1.0k citations

Peers

Countries citing papers authored by James Mull

Since Specialization

Citations

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

Fields of papers citing papers by James Mull

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside James Mull, 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 James Mull Line = papers co-authored together James Mull links everyone, so they are left out of the graph.

All Works

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19 of 19 papers shown

#	Work
1	Tissue-Specific Expression of a Splicing Mutation in the Gene Causes Familial Dysautonomia The American Journal of Human Genetics ·Susan A. Slaugenhaupt, Anat Blumenfeld, Sandra Gill, Maire Leyne, James Mull, Math P. Cuajungco, Christopher B. Liebert, Brian P. Chadwick, Maria Idelson, Luba Reznik, Christiane M. Robbins, Izabela Makałowska, Michael Brownstein, Daniel Krappmann, Claus Scheidereit, Channa Maayan, Felicia B. Axelrod, James F. Gusella	2001	448
2	Tissue-Specific Reduction in Splicing Efficiency of IKBKAP Due to the Major Mutation Associated with Familial Dysautonomia The American Journal of Human Genetics ·Math P. Cuajungco, Maire Leyne, James Mull, Sandra Gill, Lu W, David Zagzag, Felicia B. Axelrod, Channa Maayan, James F. Gusella, Susan A. Slaugenhaupt	2003	108
3	Loss of Mouse Ikbkap, a Subunit of Elongator, Leads to Transcriptional Deficits and Embryonic Lethality That Can Be Rescued by Human IKBKAP Molecular and Cellular Biology ·Yei‐Tsung Chen, Matthew M. Hims, Ranjit S. Shetty, James Mull, Lijuan Liu, Maire Leyne, Susan A. Slaugenhaupt	2008	100
4	Kinetin Improves IKBKAP mRNA Splicing in Patients With Familial Dysautonomia Pediatric Research ·Felicia B. Axelrod, Leonard Liebes, Gabrielle Gold‐von Simson, Sandra Mendoza, James Mull, Maire Leyne, Lucy Norcliffe‐Kaufmann, Horacio Kaufmann, Susan A. Slaugenhaupt	2011	72
5	Precise Genetic Mapping and Haplotype Analysis of the Familial Dysautonomia Gene on Human Chromosome 9q31 The American Journal of Human Genetics ·Anat Blumenfeld, Susan A. Slaugenhaupt, Christopher B. Liebert, Violeta Temper, Channa Maayan, Sandra Gill, Diane Lucente, Maria Idelson, Kathy MacCormack, Mary Anne Monahan, James Mull, Maire Leyne, Marc L. Mendillo, Taryn A. Schiripo, Esther Mishori, Xandra O. Breakefield, Felicia B. Axelrod, James F. Gusella	1999	53
6	Identification of the first non‐Jewish mutation in familial Dysautonomia American Journal of Medical Genetics Part A ·Maire Leyne, James Mull, Sandra Gill, Math P. Cuajungco, Carole Oddoux, Anat Blumenfeld, Channa Maayan, James F. Gusella, Felicia B. Axelrod, Susan A. Slaugenhaupt	2003	53
7	Therapeutic potential and mechanism of kinetin as a treatment for the human splicing disease familial dysautonomia Journal of Molecular Medicine ·Matthew M. Hims, El Chérif Ibrahim, Maire Leyne, James Mull, Lijuan Liu, Conxi Lázaro, Ranjit S. Shetty, Sandra Gill, James F. Gusella, Robin Reed, Susan A. Slaugenhaupt	2007	48
8	A humanized IKBKAP transgenic mouse models a tissue-specific human splicing defect Genomics ·Matthew M. Hims, Ranjit S. Shetty, James Pickel, James Mull, Maire Leyne, Lijuan Liu, James F. Gusella, Susan A. Slaugenhaupt	2007	41
9	Cloning, Mapping, and Expression of Two Novel Actin Genes, Actin-like-7A (ACTL7A) and Actin-like-7B (ACTL7B), from the Familial Dysautonomia Candidate Region on 9q31 Genomics ·Brian P. Chadwick, James Mull, L.A. Helbling, Sandra Gill, Maire Leyne, Christiane M. Robbins, Heather W. Pinkett, Izabela Makałowska, Channa Maayan, Anat Blumenfeld, Felicia B. Axelrod, M J Brownstein, James F. Gusella, Susan A. Slaugenhaupt	1999	32
10	Kinetin in Familial Dysautonomia Carriers: Implications for a New Therapeutic Strategy Targeting mRNA Splicing Pediatric Research ·Gabrielle Gold‐von Simson, Judith D. Goldberg, Linda Rolnitzky, James Mull, Maire Leyne, Andrei Voustianiouk, Susan A. Slaugenhaupt, Felicia B. Axelrod	2009	30
11	Cloning, Characterization, and Genomic Structure of the Mouse Ikbkap Gene DNA and Cell Biology ·Math P. Cuajungco, Maire Leyne, James Mull, Sandra Gill, James F. Gusella, Susan A. Slaugenhaupt	2001	23
12	Immunity to Chlamydial Infections of the Eye II. Studies of Passively Transferred Serum Antibody in Resistance to Infection with Guinea Pig Inclusion Conjunctivitis Infection and Immunity ·Ronald R. Watson, James Mull, Alexander MacDonald, Sumner E. Thompson, S E Bear	1973	22
13	Fludrocortisone in patients with familial dysautonomia Clinical Autonomic Research ·Felicia B. Axelrod, Judith D. Goldberg, Linda Rolnitzky, James Mull, Sandra P. Mann, Gabrielle Gold‐von Simson, Dena Berlin, Susan A. Slaugenhaupt	2005	16
14	Immunity to Chlamydial Infections of the Eye V. Passive Transfer of Antitrachoma Antibodies to Owl Monkeys Infection and Immunity ·Neil S. Orenstein, James Mull, Sumner E. Thompson	1973	15
15	The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene Genomics ·Susan A. Slaugenhaupt, Anat Blumenfeld, Christopher B. Liebert, James Mull, Diane Lucente, Marianne Monahan, Xandra O. Breakefield, Channa Maayan, Luis F. Parada, Felicia B. Axelrod, James F. Gusella	1995	8
16	IKBKAP mRNA in Peripheral Blood Leukocytes: A Molecular Marker of Gene Expression and Splicing in Familial Dysautonomia Pediatric Research ·Gabrielle Gold‐von Simson, Maire Leyne, James Mull, Linda Rolnitzky, Judith D. Goldberg, Dena Berlin, Felicia B. Axelrod, Susan A. Slaugenhaupt	2008	8
17	Cloning, mapping, and expression of a novel brain-specific transcript in the Familial Dysautonomia candidate region on Chromosome 9q31 Mammalian Genome ·Brian P. Chadwick, Maire Leyne, Sandra Gill, Christopher B. Liebert, James Mull, Éva Mezey, Christiane M. Robbins, Heather W. Pinkett, Izabela Makałowska, Channa Maayan, Anat Blumenfeld, Felicia B. Axelrod, M J Brownstein, James F. Gusella, Susan A. Slaugenhaupt	2000	5
18	Immunoglobulins, Secretory Component, and Transferrin in Eye Secretions of Infants in Regions With and Without Endemic Trachoma Infection and Immunity ·James Mull, John H. Peters, Roger Nichols	1970	4
19	Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 gene Gene ·Brian P. Chadwick, Sandra Gill, Maire Leyne, James Mull, Christopher B. Liebert, Christiane M. Robbins, Heather W. Pinkett, Izabela Makałowska, Channa Maayan, Anat Blumenfeld, Felicia B. Axelrod, M J Brownstein, Susan A. Slaugenhaupt	1999	3

About James Mull

James Mull is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Cell Biology, Neurology and Microbiology, having authored 19 papers that have together received 1.1k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (15 papers), RNA Research and Splicing (5 papers), RNA regulation and disease (5 papers), Signaling Pathways in Disease (4 papers), Neurological diseases and metabolism (3 papers), Reproductive tract infections research (3 papers), Cellular Mechanics and Interactions (3 papers) and Endoplasmic Reticulum Stress and Disease (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (595 citations), Neurology (141 citations), Cell Biology (227 citations), Molecular Biology (624 citations) and Genetics (63 citations). James Mull has collaborated with scholars based in United States, Israel and Saudi Arabia. Frequent co-authors include Susan A. Slaugenhaupt, Maire Leyne, Felicia B. Axelrod, James F. Gusella, Sandra Gill, Channa Maayan, Math P. Cuajungco, Anat Blumenfeld, Christopher B. Liebert and Maria Idelson. Their work appears in journals such as The American Journal of Human Genetics, Infection and Immunity, Pediatric Research, Genomics and Gene.

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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