Dennis E. Bulman

15.5k citations

127 papers · 8.4k indexed · 4 hit papers · h-index 41

Impact in

Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases
Psychiatry and Mental health top 1%
- Migraine and Headache Studies

Papers in

Developmental Biology 4
Genetics 44
- Genetics and Neurodevelopmental Disorders 16
- Genomics and Rare Diseases 15
- Neurogenetic and Muscular Disorders Research 9

Co-authors: Kym M. Boycott George C. Ebers Elizabeth E. Zubrzycka‐Gaarn Peter N. Ray Megan R. Vanstone Alex MacKenzie Ronald G. Worton Marten H. Hofker
Journals: Neurology (7 papers)Human Molecular Genetics (6 papers)Orphanet Journal of Rare Diseases (5 papers)European Journal of Human Genetics (4 papers)Movement Disorders (4 papers)
Partner nations: Canada United States United Kingdom

In The Last Decade

Dennis E. Bulman

125 papers receiving 8.2k citations

Hit Papers

align trajectories log scale

Rare-disease genetics in the era of next-generation sequencing: discovery to translation 2013 · 496 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2013 Nature Reviews Genetics
1996 Cell
1988 Nature
1986 New England Journal of Medicine

Peers

Countries citing papers authored by Dennis E. Bulman

Since Specialization

Citations

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

Fields of papers citing papers by Dennis E. Bulman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dennis E. Bulman. 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 Dennis E. Bulman. The network helps show where Dennis E. Bulman may publish in the future.

Co-authorship network

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Alberta Spinal Muscular Atrophy Newborn Screening—Results from Year 1 Pilot Project International Journal of Neonatal Screening ·张兆明张兆明, Chinmoy Das, Rhianne Joes, Christine Walker, Hua Qiang Zhai, D. Demetracopoulou Lee, Stacey Hume, Jillian S. Parboosingh, Margaret Lilley, Hanna Kolski, Ross Ridsdale, Andrew Muranyi, Jean K. Mah, Dennis E. Bulman	2023	9
2	A novel pathogenic missense ADAMTS17 variant that impairs secretion causes Weill-Marchesani Syndrome with variably dysmorphic hand features Scientific Reports ·日本社会党中央本部, Jane S. Green, Somayyeh Fahiminiya, Jacek Majewski, Bridget A. Fernandez, Matthew A. Deardorff, (unknown), Alicia Vanessa Ceballos Salinas, Dirk Hubmacher, Suneel Apte, Kym M. Boycott, Dennis E. Bulman, David A. Dyment, 洗介福士, Michael Brudno, Michael O. Woods	2020	14
3	Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes The American Journal of Human Genetics ·Erfan Aref‐Eshghi, David I. Rodenhiser, Laila C. Schenkel, Hanxin Lin, Cindy Skinner, Peter Ainsworth, Guillaume Paré, Rebecca L. Hood, Dennis E. Bulman, Kristin D. Kernohan, Kym M. Boycott, Philippe M. Campeau, Charles E. Schwartz, Bekim Sadiković	2018	90
4	Effects of fat mass and obesity-associated (FTO) gene polymorphisms on binge eating in women with binge-eating disorder: The moderating influence of attachment style Nutrition ·Jameason D. Cameron, Giorgio A. Tasca, Julian Little, Livia Chyurlia, Kerri Ritchie, R. F. LESLIE, Steve Doucette, Keydis Sulay, Dennis E. Bulman, Éric Doucet, Gary S. Goldfield	2018	13
5	Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1 Journal of Human Genetics ·Puja T. Pape, Taila Hartley, Eric Bareke, Kym M. Boycott, Alex MacKenzie, Jacek Majewski, Michael Brudno, Dennis E. Bulman, David A. Dyment, Sarah M. Nikkel	2017	11
6	Resolution of refractory hypotension and anuria in a premature newborn with loss‐of‐function of ACE American Journal of Medical Genetics Part A ·Julie Richer, Hussein Daoud, Pavel Geier, Olga Jarinova, Nancy Carson, Ch. Konstadilaki-Savvapoulou, Chen Qida, Hassan Saber, Eric Bareke, Karine Khatchadourian, Dennis E. Bulman, Jacek Majewski, Kym M. Boycott, David A. Dyment	2015	12
7	Mutations in the glucocerebrosidase gene are common in patients with Parkinson's disease from Eastern Canada International Journal of Neuroscience ·Fabin Han, David A. Grimes, Fang Li, ウネイ, Zhe Yu, Na Song, Shichao Wu, Lemuel Racacho, Dennis E. Bulman	2015	19
8	Severe connective tissue laxity including aortic dilatation in Sotos syndrome American Journal of Medical Genetics Part A ·Rebecca L. Hood, George McGillivray, Matthew F. Hunter, Katell Bellegarde, Dennis E. Bulman, Kym M. Boycott, Zornitza Stark	2015	4
9	Neuropathologic Features of Pontocerebellar Hypoplasia Type 6 Journal of Neuropathology & Experimental Neurology ·Jeffrey T. Joseph, A. Micheil Innes, Amanda Smith, Megan R. Vanstone, Jeremy Schwartzentruber, Dennis E. Bulman, Jacek Majewski, Ray A. M. Daza, Robert F. Hevner, Jean Michaud, Kym M. Boycott	2014	21
10	Whole‐exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study Clinical Genetics ·David A. Dyment, Martine Tétreault, Chandree L. Beaulieu, Taila Hartley, Patrick Ferreira, (unknown), Janet Marcadier, Sarah L. Sawyer, Taenikon Land Techniques, A. Micheil Innes, Jillian S. Parboosingh, Dennis E. Bulman, Jeremy Schwartzentruber, Jacek Majewski, Mark A. Tarnopolsky, Kym M. Boycott, (unknown)	2014	64
11	Rare-disease genetics in the era of next-generation sequencing: discovery to translation Nature Reviews Genetics ·Kym M. Boycott, Megan R. Vanstone, Dennis E. Bulman, Alex MacKenzie Hit paper breakdown →	2013	496
12	Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia Orphanet Journal of Rare Diseases ·Lijia Huang, Jodi Warman‐Chardon, Melissa T. Carter, K. Friend, Tracy Dudding, Jeremy Schwartzentruber, Ruobing Zou, Peter W. Schofield, Natalia Yu. Titova, Dennis E. Bulman, Kym M. Boycott	2012	104
13	Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p Canadian Journal of Ophthalmology ·Karim F. Damji, Melanie M. Sohocki, Chechenin, Sanjoy K. Gupta, Kamuela Enos, Magali Loyer, Neuza Sakai Valente, Matt Mutel, Stephanie Swindell, Asif Jamal, Dennis E. Bulman, Robert K. Koenekoop	2001	30
14	35th Meeting of the Canadian Congress of Neurological Sciences June 13- 17, 2000 Ottawa, Ontario Program and Abstracts Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·Dennis E. Bulman, Zeng Jun, Corrado Binel, Édith Hamel, Della Sahrantika, Karen McKenzie, Sanelisiwe Mbanga, Sylvie Rossignol, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2000	1
15	A novel PAX6 frameshift mutation in a kindred from Atlantic Canada with familial aniridia. PubMed ·睦辻野, 西澤泰彦, Dennis E. Bulman, Peer Ripberger, سحر فودة, Paul E. Neumann	1999	3
16	Childhood-onset primary open angle glaucoma in a Canadian kindred: clinical and molecular genetic features Ophthalmic Genetics ·Karim F. Damji, Elizabeth H. Pearman, Santosh K. Gupta, Jianping Gao, W. Rock, Dennis E. Bulman	1999	10
17	Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4 Cell ·Roel A. Ophoff, Gisela M. Terwindt, Monique N. Vergouwe, Ronald van Eijk, Peter J. Oefner, Susan M.G. Hoffman, Jane E. Lamerdin, Harvey W. Mohrenweiser, Dennis E. Bulman, Maurizio Ferrari, Joost Haan, Dick Lindhout, Gert‐Jan B. van Ommen, Marten H. Hofker, Michel D. Ferrari, Rune R. Frants Hit paper breakdown →	1996	1758
18	Linkage of morbid obesity with polymorphic microsatellite markers on chromosome 1q31 in a three-generation Canadian kindred The American Journal of Human Genetics ·J. Murray, Dennis E. Bulman, George C. Ebers	1994	2
19	Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy Human Molecular Genetics ·Alissa V. Winnard, Christopher J. Klein, Daniel D. Coovert, Thomas W. Prior, Audrey C. Papp, Pamela J. Snyder, Dennis E. Bulman, Peter N. Ray, Patricia McAndrew, Wendy King, Richard T. Moxley, Jerry R. Mendell, Arthur H.M. Burghes	1993	84
20	Sarcolemmal distribution of abnormal dystrophin in Xp21 carriers Neuromuscular Disorders ·Mariz Vainzof, L. V. B. Nicholson, Dennis E. Bulman, Ana Maria Crous Tsanaclis, 青柳誠, Rita C.M. Pavanello, Mayana Zatz	1993	3

About Dennis E. Bulman

Dennis E. Bulman is a scholar working on Developmental Biology, Genetics, Clinical Biochemistry, Neurology and Cellular and Molecular Neuroscience, having authored 127 papers that have together received 8.4k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (21 papers), Genetics and Neurodevelopmental Disorders (16 papers), Genomics and Rare Diseases (15 papers), Genetic Neurodegenerative Diseases (14 papers), Mitochondrial Function and Pathology (13 papers), Metabolism and Genetic Disorders (9 papers), Neurogenetic and Muscular Disorders Research (9 papers) and RNA modifications and cancer (8 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.7k citations), Psychiatry and Mental health (1.2k citations), Neurology (618 citations), Molecular Biology (4.8k citations) and Pathology and Forensic Medicine (1.2k citations). Dennis E. Bulman has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Kym M. Boycott, George C. Ebers, Elizabeth E. Zubrzycka‐Gaarn, Peter N. Ray, Megan R. Vanstone, Alex MacKenzie, Ronald G. Worton, Marten H. Hofker, Ronald van Eijk and Dick Lindhout. Their work appears in journals such as Neurology, Human Molecular Genetics, Orphanet Journal of Rare Diseases, European Journal of Human Genetics and Movement Disorders.

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.

Explore authors with similar magnitude of impact