Nicole C. Meyer

7.3k citations

44 papers · 2.4k indexed · h-index 28

Immunology top 2%
Molecular Biology top 10%
Nephrology top 0.5%
Hematology top 2%
Sensory Systems top 1%

Co-authors: Richard J. Smith Yuzhou Zhang Carla Nester Hossein Najmabadi Kimia Kahrizi Susan StromeKai WangSanjeev Sethi
Topics: Complement system in diseases (16 papers)Renal Diseases and Glomerulopathies (15 papers)Hearing, Cochlea, Tinnitus, Genetics (11 papers)
Cited by: Aging Nephrology Sensory Systems
Journals: PLANT PHYSIOLOGY Current Biology Genetics
Partner nations: United States Iran Belgium

In The Last Decade

Nicole C. Meyer

43 papers receiving 2.3k citations

Peers

Countries citing papers authored by Nicole C. Meyer

Since Specialization

Citations

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

Fields of papers citing papers by Nicole C. Meyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicole C. Meyer

This figure shows the co-authorship network connecting the top 25 collaborators of Nicole C. Meyer. A scholar is included among the top collaborators of Nicole C. Meyer 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 Nicole C. Meyer. Nicole C. Meyer 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	Defining Nephritic Factors as Diverse Drivers of Systemic Complement Dysregulation in C3 Glomerulopathy 2023 ·Kidney International Reports ·(unknown),(unknown),(unknown),Amanda Taylor,Nicole C. Meyer,Sarah M. Roberts,(unknown),(unknown),Nicolò Ghiringhelli Borsa,(unknown),Carla Nester,Richard J. Smith	8
2	Factor H Autoantibodies and Complement-Mediated Diseases 2020 ·Frontiers in Immunology ·Yuzhou Zhang,Nicolò Ghiringhelli Borsa,(unknown),(unknown),(unknown),Nicole C. Meyer,(unknown),Amanda Taylor,Carla Nester,Christoph Q. Schmidt,Richard J. Smith	27
3	Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic Syndrome 2018 ·Journal of the American Society of Nephrology ·Fengxiao Bu,Yuzhou Zhang,Kai Wang,Nicolò Ghiringhelli Borsa,M. B. Jones,Amanda Taylor,(unknown),Nicole C. Meyer,Kathy Frees,Christie P. Thomas,Carla Nester,Richard J. Smith	48
4	High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies 2015 ·Journal of the American Society of Nephrology ·Fengxiao Bu,Nicolò Ghiringhelli Borsa,M. B. Jones,(unknown),Carla Nishimura,(unknown),Héla Azaiez,E. Ann Black-Ziegelbein,Nicole C. Meyer,Diana L. Kolbe,Yingyue Li,Kathy Frees,Michael J. Schnieders,Christie P. Thomas,Carla Nester,Richard J. Smith	74
5	Rare Variants in BMP2 and BMP4 Found in Otosclerosis Patients Reduce Smad Signaling 2014 ·Otology & Neurotology ·Megan Ealy,Nicole C. Meyer,(unknown),Isabelle Schrauwen,(unknown),Markus Pfister,Guy Van Camp,Richard J. Smith	10
6	Defining the Complement Biomarker Profile of C3 Glomerulopathy 2014 ·Clinical Journal of the American Society of Nephrology ·Yuzhou Zhang,Carla Nester,(unknown),Mikkel‐Ole Skjoedt,Nicole C. Meyer,(unknown),Nicolò Ghiringhelli Borsa,Yaseelan Palarasah,Richard J. Smith	66
7	Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome 2013 ·Journal of the American Society of Nephrology ·Fengxiao Bu,Tara Maga,Nicole C. Meyer,Kai Wang,Christie P. Thomas,Carla Nester,Richard J. Smith	161
8	Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement 2012 ·Kidney International ·Sanjeev Sethi,Fernando C. Fervenza,Yuzhou Zhang,Ladan Zand,Nicole C. Meyer,Nicolò Ghiringhelli Borsa,Samih H. Nasr,Richard J. Smith	139
9	Causes of Alternative Pathway Dysregulation in Dense Deposit Disease 2012 ·Clinical Journal of the American Society of Nephrology ·Yuzhou Zhang,Nicole C. Meyer,Kai Wang,Carla Nishimura,Kathy Frees,Michael P. Jones,Louis M. Katz,Sanjeev Sethi,Richard J. Smith	147
10	Functional Variants in NOS1 and NOS2A Are Not Associated with Progressive Hearing Loss in Ménière's Disease in a European Caucasian Population 2011 ·DNA and Cell Biology ·Irene Gázquez,José A. López‐Escámez,Antonia Ruíz Moreno,Colleen A. Campbell,Nicole C. Meyer,John P. Carey,Lloyd B. Minor,Bruce J. Gantz,Marlan R. Hansen,Charles C. Della Santina,Ismael Arán,Andrés Soto-Varela,(unknown),Ángel Batuecas Caletrío,Herminio Pérez-Garrigues,(unknown),Richard J. Smith,Miguel Ángel López‐Nevot	9
11	Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss 2011 ·American Journal of Medical Genetics Part A ·Niloofar Bazazzadegan,(unknown),(unknown),Kimia Kahrizi,Nicole C. Meyer,Guy Van Camp,Nele Hilgert,Seyedeh Sedigheh Abedini,(unknown),Ahmad Daneshi,Carla Nishimura,Matthew R. Avenarius,Mohammad Farhadi,Richard J. Smith,Hossein Najmabadi	7
12	Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations 2009 ·Human Genetics ·Isabelle Schrauwen,Megan Ealy,Erik Fransén,Kathleen Vanderstraeten,Melissa Thys,Nicole C. Meyer,(unknown),Alexander Huber,Manuela Mazzoli,Markus Pfister,Richard J. Smith,Guy Van Camp	24
13	Human Male Infertility Caused by Mutations in the CATSPER1 Channel Protein 2009 ·The American Journal of Human Genetics ·Matthew R. Avenarius,Michael S. Hildebrand,Yuzhou Zhang,Nicole C. Meyer,(unknown),Kimia Kahrizi,Hossein Najmabadi,Richard J. Smith	177
14	Comparative linkage analysis and visualization of high-density oligonucleotide SNP array data 2005 ·BMC Genetics ·Igor Leykin,Ke Hao,(unknown),Nicole C. Meyer,Martin R. Pollak,Richard J. Smith,Wing Hung Wong,Carsten Rosenow,Cheng Li	20
15	The PGL Family Proteins Associate With Germ Granules and Function Redundantly in Caenorhabditis elegans Germline Development 2004 ·Genetics ·Ichiro Kawasaki,Anahita Amiri,Yuan Fan,Nicole C. Meyer,(unknown),Tomoko Motohashi,Takeshi Karashima,Olaf Bossinger,Susan Strome	106
16	C. elegans PAR Proteins Function by Mobilizing and Stabilizing Asymmetrically Localized Protein Complexes 2004 ·Current Biology ·(unknown),Julie C. Canman,Willow N. Gabriel,Nicole C. Meyer,Susan Strome,Bob Goldstein	153
17	Branchio-oto-renal syndrome: The mutation spectrum inEYA1and its phenotypic consequences 2004 ·Human Mutation ·Eugene H. Chang,Maithilee Menezes,Nicole C. Meyer,Robert A. Cucci,Virginie Vervoort,Charles E. Schwartz,Richard J. Smith	159
18	Clone–Contig and STS Maps of the Hereditary Hemochromatosis Region on Human Chromosome 6p21.3–p22 1997 ·Genome Research ·Peter Lauer,Nicole C. Meyer,(unknown),Steven M. Starnes,Roger K. Wolff,Andreas Gnirke	20
19	A 1.1-Mb Transcript Map of the Hereditary Hemochromatosis Locus 1997 ·Genome Research ·David A. Ruddy,(unknown),Vince Lee,Gabriel A. Mintier,Leah Quintana,(unknown),Nicole C. Meyer,Alivelu Irrinki,Erin E. McClelland,(unknown),Felipa Mapa,Theodore B. Moore,Winston Thomas,Deborah B. Loeb,Cyrus L. Harmon,Zenta Tsuchihashi,Roger K. Wolff,Randall C. Schatzman,John N. Feder	71
20	Nucleotide Sequence of a Gene Encoding a 58.5-Kilodalton Barley Dehydrin That Lacks a Serine Tract 1995 ·PLANT PHYSIOLOGY ·Timothy J. Close,Nicole C. Meyer,J Radik	22

About Nicole C. Meyer

Nicole C. Meyer is a scholar working on Sensory Systems, Nephrology and Aging, having authored 44 papers that have together received 2.4k indexed citations. Recurring topics across this work include Complement system in diseases (16 papers), Renal Diseases and Glomerulopathies (15 papers) and Hearing, Cochlea, Tinnitus, Genetics (11 papers). The work is most often cited by research in Aging (235 citations), Nephrology (740 citations) and Sensory Systems (311 citations). Nicole C. Meyer has collaborated with scholars based in United States, Iran and Belgium. Frequent co-authors include Richard J. Smith, Yuzhou Zhang, Carla Nester, Hossein Najmabadi, Kimia Kahrizi, Susan Strome, Kai Wang, Sanjeev Sethi, Nicolò Ghiringhelli Borsa and Fengxiao Bu. Their work appears in journals such as PLANT PHYSIOLOGY, Current Biology and Genetics.

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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