Matthew C. Dulik

3.7k total citations
28 papers, 647 citations indexed

About

Matthew C. Dulik is a scholar working on Genetics, Molecular Biology and General Health Professions. According to data from OpenAlex, Matthew C. Dulik has authored 28 papers receiving a total of 647 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 7 papers in Molecular Biology and 3 papers in General Health Professions. Recurrent topics in Matthew C. Dulik's work include Forensic and Genetic Research (14 papers), Genetic diversity and population structure (9 papers) and Genomics and Rare Diseases (5 papers). Matthew C. Dulik is often cited by papers focused on Forensic and Genetic Research (14 papers), Genetic diversity and population structure (9 papers) and Genomics and Rare Diseases (5 papers). Matthew C. Dulik collaborates with scholars based in United States, Russia and Argentina. Matthew C. Dulik's co-authors include Theodore G. Schurr, L. P. Osipova, Sergey Zhadanov, Ömer Gökçümen, Samara Rubinstein, Nancy B. Spinner, Athma A. Pai, Timothy R. Rebbeck, A. H. C. Walker and Klara Stefflova and has published in prestigious journals such as Blood, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Matthew C. Dulik

26 papers receiving 625 citations

Peers

Countries citing papers authored by Matthew C. Dulik

Since Specialization

Citations

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

Fields of papers citing papers by Matthew C. Dulik

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew C. Dulik. 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 Matthew C. Dulik. The network helps show where Matthew C. Dulik may publish in the future.

Co-authorship network of co-authors of Matthew C. Dulik

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew C. Dulik. A scholar is included among the top collaborators of Matthew C. Dulik 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 Matthew C. Dulik. Matthew C. Dulik 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	Clinical Characteristics of Patients With Kabuki Syndrome at a Single Tertiary Children's Hospital 2025 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Elizabeth T. DeChene, Melissa A. Gilbert, Matthew C. Dulik, (unknown), Kosuke Izumi	0
2	Advanced approach for comprehensive mtDNA genome testing in mitochondrial disease 2021 ·Molecular Genetics and Metabolism ·Jing Wang, Jorune Balciuniene, Maria Alejandra Diaz‐Miranda, Elizabeth M. McCormick, (unknown), Alison M. Muir, Kajia Cao, (unknown), (unknown), (unknown), Zarazuela Zolkipli‐Cunningham, Amy Goldstein, Rebecca Ganetzky, Colleen Muraresku, (unknown), Nancy B. Spinner, Douglas C. Wallace, Matthew C. Dulik, Marni J. Falk	9
3	Genomic Diagnosis for Pediatric Disorders: Revolution and Evolution 2020 ·Frontiers in Pediatrics ·Emilie Lalonde, Stefan Rentas, Fumin Lin, Matthew C. Dulik, Cara Skraban, Nancy B. Spinner	30
4	Mitochondrial single-stranded DNA binding protein novel de novo SSBP1 mutation in a child with single large-scale mtDNA deletion (SLSMD) clinically manifesting as Pearson, Kearns-Sayre, and Leigh syndromes 2019 ·PLoS ONE ·(unknown), Elizabeth M. McCormick, L. Perera, Matthew J. Longley, Renkui Bai, Jianping Kong, Matthew C. Dulik, Li Shen, Amy Goldstein, Shana E. McCormack, Benjamin L. Laskin, Bart P. Leroy, Xilma R. Ortiz‐González, (unknown), William C. Copeland, Marni J. Falk	31
5	AUDIOME: a tiered exome sequencing–based comprehensive gene panel for the diagnosis of heterogeneous nonsyndromic sensorineural hearing loss 2018 ·Genetics in Medicine ·Qiaoning Guan, Jorune Balciuniene, Kajia Cao, (unknown), Sawona Biswas, Alisha Wilkens, (unknown), Emma Bedoukian, Jennifer Tarpinian, Pushkala Jayaraman, Mahdi Sarmady, Matthew C. Dulik, Avni Santani, Nancy B. Spinner, Ahmad Abou Tayoun, Ian D. Krantz, Laura K. Conlin, Minjie Luo	27
6	Utility and limitations of exome sequencing in the molecular diagnosis of pediatric inherited platelet disorders 2017 ·American Journal of Hematology ·Edward J. Romasko, Batsal Devkota, Sawona Biswas, (unknown), Ramakrishnan Rajagopalan, Matthew C. Dulik, Christopher S. Thom, (unknown), (unknown), Maria I. Scarano, Ian D. Krantz, Nancy B. Spinner, Laura K. Conlin, Michele P. Lambert	22
7	Clinical phenotype-based gene prioritization: an initial study using semantic similarity and the human phenotype ontology 2014 ·BMC Bioinformatics ·Aaron J. Masino, Elizabeth T. DeChene, Matthew C. Dulik, Alisha Wilkens, Nancy B. Spinner, Ian D. Krantz, Jeffrey W. Pennington, Peter N. Robinson, Peter S. White	43
8	Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium 2013 ·Genetics in Medicine ·Jonathan S. Berg, Laura M. Amendola, Christine M. Eng, Eliezer M. Van Allen, Stacy W. Gray, Nikhil Wagle, Heidi L. Rehm, Elizabeth T. DeChene, Matthew C. Dulik, Fuki M. Hisama, Wylie Burke, Nancy B. Spinner, Levi A. Garraway, Robert C. Green, Sharon E. Plon, James P. Evans, Gail P. Jarvik	86
9	Genetic Background and Climatic Droplet Keratopathy Incidence in a Mapuche Population from Argentina 2013 ·PLoS ONE ·Theodore G. Schurr, Matthew C. Dulik, (unknown), (unknown), Julio A. Urrets‐Zavalía, Horacio M. Serra	6
10	The timing and process of the colonization of South America: a North American perspective 2012 ·Theodore G. Schurr, Matthew C. Dulik, Miguel G. Vilar, Amanda C. Owings, Jill B. Gaieski	2
11	Genetic variation in Mi’kmaq populations from Nova Scotia and its implications for the history of Algonquian populations in northeastern North America 2012 ·Amanda C. Owings, Matthew C. Dulik, Sergey Zhadanov, Jill B. Gaieski, (unknown), (unknown), Theodore G. Schurr	1
12	Mitochondrial DNA and Y Chromosome Variation Provides Evidence for a Recent Common Ancestry between Native Americans and Indigenous Altaians 2012 ·The American Journal of Human Genetics ·Matthew C. Dulik, Sergey Zhadanov, L. P. Osipova, (unknown), (unknown), Ömer Gökçümen, Samara Rubinstein, Theodore G. Schurr	105
13	Clan, language, and migration history has shaped genetic diversity in Haida and Tlingit populations from Southeast Alaska 2012 ·American Journal of Physical Anthropology ·Theodore G. Schurr, Matthew C. Dulik, Amanda C. Owings, Sergey Zhadanov, Jill B. Gaieski, Miguel G. Vilar, (unknown), (unknown), (unknown)	33
14	Dissecting the Within-Africa Ancestry of Populations of African Descent in the Americas 2011 ·PLoS ONE ·Klara Stefflova, Matthew C. Dulik, Jill S. Barnholtz‐Sloan, Athma A. Pai, A. H. C. Walker, Timothy R. Rebbeck	43
15	Y-Chromosome Variation in Altaian Kazakhs Reveals a Common Paternal Gene Pool for Kazakhs and the Influence of Mongolian Expansions 2011 ·PLoS ONE ·Matthew C. Dulik, L. P. Osipova, Theodore G. Schurr	53
16	Genetic heritage and native identity of the Seaconke Wampanoag tribe of massachusetts 2010 ·American Journal of Physical Anthropology ·Sergey Zhadanov, Matthew C. Dulik, (unknown), (unknown), Jill B. Gaieski, George Elias, Theodore G. Schurr	12
17	Evaluation of Group Genetic Ancestry of Populations from Philadelphia and Dakar in the Context of Sex-Biased Admixture in the Americas 2009 ·PLoS ONE ·Klara Stefflova, Matthew C. Dulik, Athma A. Pai, A. H. C. Walker, Charnita Zeigler‐Johnson, Serigne M. Gueye, Theodore G. Schurr, Timothy R. Rebbeck	33
18	Russian Old Believers: Genetic Consequences of Their Persecution and Exile, as Shown by Mitochondrial DNA Evidence 2008 ·Human Biology ·Samara Rubinstein, Matthew C. Dulik, Ömer Gökçümen, Sergey Zhadanov, L. P. Osipova, (unknown), (unknown), Marina Gubina, Olga L. Posukh, Theodore G. Schurr	10
19	Genetic variation in the enigmatic Altaian Kazakhs of South‐Central Russia: Insights into Turkic population history 2008 ·American Journal of Physical Anthropology ·Ömer Gökçümen, Matthew C. Dulik, Athma A. Pai, Sergey Zhadanov, Samara Rubinstein, L. P. Osipova, (unknown), (unknown), Marina Gubina, Damian Labuda, Theodore G. Schurr	36
20	Russian Old Believers: Genetic Consequences of Their Persecution and Exile, as Shown by Mitochondrial DNA Evidence 2008 ·Human Biology ·Samara Rubinstein, Matthew C. Dulik, Ömer Gökçümen, Sergey Zhadanov, L. P. Osipova, (unknown), (unknown), Marina Gubina, Olga L. Posukh, Theodore G. Schurr	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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