Andrew R. Cullinane

2.2k citations

20 papers · 824 indexed · h-index 16

Genetics top 5%
Molecular Biology
Cell Biology top 10%
Immunology
Pediatrics, Perinatology and Child Health top 10%

Co-authors: Marjan Huizing Alejandro A. Schäffer William A. Gahl Konrad Krzewski Thierry Vilboux Meral Gunay‐Aygun Helen R. Dawe Déirdre Kelly
Topics: melanin and skin pigmentation (6 papers)Autoimmune and Inflammatory Disorders Research (5 papers)Immune Cell Function and Interaction (4 papers)
Cited by: Genetics Cell Biology Hematology
Journals: Journal of Allergy and Clinical Immunology Human Molecular Genetics Journal of Investigative Dermatology
Partner nations: United States United Kingdom France

In The Last Decade

Andrew R. Cullinane

20 papers receiving 813 citations

Peers

Countries citing papers authored by Andrew R. Cullinane

Since Specialization

Citations

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

Fields of papers citing papers by Andrew R. Cullinane

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew R. Cullinane. 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 Andrew R. Cullinane. The network helps show where Andrew R. Cullinane may publish in the future.

Co-authorship network of co-authors of Andrew R. Cullinane

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew R. Cullinane. A scholar is included among the top collaborators of Andrew R. Cullinane 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 Andrew R. Cullinane. Andrew R. Cullinane 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	Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center 2017 ·Genetics in Medicine ·Thierry Vilboux,Dan Doherty,Ian A. Glass,Melissa A. Parisi,Ian G. Phelps,Andrew R. Cullinane,Wadih M. Zein,Brian P. Brooks,Theo Heller,Ariane Soldatos,Neal L. Oden,(unknown),Meghana Vemulapalli,James C. Mullikin,May Christine V. Malicdan,William A. Gahl,Meral Gunay‐Aygun	88
2	CELSR2, encoding a planar cell polarity protein, is a putative gene in Joubert syndrome with cortical heterotopia, microophthalmia, and growth hormone deficiency 2017 ·American Journal of Medical Genetics Part A ·Thierry Vilboux,May Christine V. Malicdan,Joseph C. Roney,Andrew R. Cullinane,Joshi Stephen,(unknown),Joy Bryant,Roxanne Fischer,Meghana Vemulapalli,James C. Mullikin,(unknown),Peter Steinbach,William A. Gahl,Meral Gunay‐Aygun	24
3	Joubert syndrome: neuroimaging findings in 110 patients in correlation with cognitive function and genetic cause 2017 ·Journal of Medical Genetics ·Andrea Poretti,Joseph Snow,Angela C. Summers,Aylin Tekes,Thierry A.G.M. Huisman,Nafi Aygün,Kathryn A. Carson,Dan Doherty,Melissa A. Parisi,Camilo Toro,(unknown),Meghana Vemulapalli,Jim Mullikin,(unknown),Andrew R. Cullinane,Thierry Vilboux,William A. Gahl,Meral Gunay‐Aygun	48
4	Natural killer cell activity and dysfunction in Hermansky‐Pudlak syndrome 2016 ·British Journal of Haematology ·Aleksandra Gil‐Krzewska,Yousuke Murakami,Giovanna Peruzzi,Kevin O’Brien,Melissa A. Merideth,Andrew R. Cullinane,William A. Gahl,John E. Coligan,Bernadette R. Gochuico,Konrad Krzewski	17
5	Identification of a novel mutation in HPS6 in a patient with hemophilia B and oculocutaneous albinism 2016 ·Molecular Genetics and Metabolism ·Kevin O’Brien,Jay N. Lozier,Andrew R. Cullinane,(unknown),Khanh Nghiem,Vladislav V. Speransky,Wadih M. Zein,James C. Mullikin,Anne T. Neff,(unknown),May Christine V. Malicdan,William A. Gahl,Lisa R. Young,Bernadette R. Gochuico	9
6	Chediak-Higashi syndrome: Lysosomal trafficking regulator domains regulate exocytosis of lytic granules but not cytokine secretion by natural killer cells 2015 ·Journal of Allergy and Clinical Immunology ·Aleksandra Gil‐Krzewska,Stephanie M. Wood,Yousuke Murakami,Victoria Nguyen,Samuel C. C. Chiang,Andrew R. Cullinane,Giovanna Peruzzi,William A. Gahl,John E. Coligan,Wendy J. Introne,Yenan T. Bryceson,Konrad Krzewski	43
7	A clinical report of Chediak–Higashi syndrome in infancy with a novel genotype from the Indian subcontinent 2015 ·International Journal of Dermatology ·Ankur Singh,(unknown),Joseph C. Roney,Andrew R. Cullinane,William A. Gahl,Nita Khurana,Seema Kapoor	3
8	In vitro functional correction of Hermansky–Pudlak Syndrome type-1 by lentiviral-mediated gene transfer 2014 ·Molecular Genetics and Metabolism ·Yasuhiro Ikawa,Richard A. Hess,Heidi Dorward,Andrew R. Cullinane,Marjan Huizing,Bernadette R. Gochuico,William A. Gahl,Fabio Candotti	12
9	Skin fibroblasts from individuals with Chediak-Higashi Syndrome (CHS) exhibit hyposensitive immunogenic response 2014 ·Orphanet Journal of Rare Diseases ·Le Wang,Kamila Rosamilia Kantovitz,Andrew R. Cullinane,Francisco Humberto Nociti,(unknown),Joseph C. Roney,A.B. Tran,Wendy J. Introne,Martha J. Somerman	6
10	The BEACH Is Hot: A LYST of Emerging Roles for BEACH‐Domain Containing Proteins in Human Disease 2013 ·Traffic ·Andrew R. Cullinane,Alejandro A. Schäffer,Marjan Huizing	118
11	Evidence for defective Rab GTPase-dependent cargo traffic in immune disorders 2013 ·Experimental Cell Research ·Konrad Krzewski,Andrew R. Cullinane	21
12	Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene 2013 ·Human Genetics ·Petcharat Leoyklang,Kanya Suphapeetiporn,Chalurmpon Srichomthong,Siraprapa Tongkobpetch,(unknown),Heidi Dorward,Andrew R. Cullinane,William A. Gahl,Marjan Huizing,Vorasuk Shotelersuk	24
13	Dysregulation of Galectin-3. Implications for Hermansky-Pudlak Syndrome Pulmonary Fibrosis 2013 ·American Journal of Respiratory Cell and Molecular Biology ·Andrew R. Cullinane,(unknown),Heidi Dorward,Carmelo Carmona‐Rivera,(unknown),Joel Moss,Kevin O’Brien,Steven D. Nathan,Keith C. Meyer,Iván O. Rosas,Amanda Helip‐Wooley,Marjan Huizing,William A. Gahl,Bernadette R. Gochuico	38
14	Chediak‐Higashi syndrome presenting as young‐onset levodopa‐responsive parkinsonism 2013 ·Movement Disorders ·Vikas Bhambhani,Wendy J. Introne,Codrin Lungu,Andrew R. Cullinane,Camilo Toro	20
15	A BLOC‐1 mutation screen reveals a novel BLOC1S3 mutation in Hermansky–Pudlak Syndrome type 8 2012 ·Pigment Cell & Melanoma Research ·Andrew R. Cullinane,(unknown),Gretchen Golas,James Pan,Carmelo Carmona‐Rivera,Richard A. Hess,James G. White,Marjan Huizing,William A. Gahl	30
16	The BLOS1‐Interacting Protein KXD1 is Involved in the Biogenesis of Lysosome‐Related Organelles 2012 ·Traffic ·Qing Yang,Xin He,Lin Yang,Zhiyong Zhou,Andrew R. Cullinane,Aihua Wei,Zhe Zhang,Zhenhua Hao,Aili Zhang,Min He,(unknown),Xiang Gao,William A. Gahl,Marjan Huizing,Wei Li	31
17	Homozygosity Mapping and Whole-Exome Sequencing to Detect SLC45A2 and G6PC3 Mutations in a Single Patient with Oculocutaneous Albinism and Neutropenia 2011 ·Journal of Investigative Dermatology ·Andrew R. Cullinane,Thierry Vilboux,Kevin O’Brien,(unknown),Dawn Maynard,Hannah Carlson-Donohoe,Carla Ciccone,NISC Comparative Sequencing Program,Thomas C. Markello,Meral Gunay‐Aygun,Marjan Huizing,William A. Gahl	52
18	Cellular and clinical report of new Griscelli syndrome type III cases 2011 ·Pigment Cell & Melanoma Research ·Wendy Westbroek,Aharon Klar,Andrew R. Cullinane,Shira G. Ziegler,Haggit Hurvitz,(unknown),(unknown),Heidi Dorward,Marjan Huizing,(unknown),(unknown),Yackov Berkun,Moran Lavie,William A. Gahl,Yair Anikster	22
19	A novel VPS33B mutation in an ARC syndrome patient presenting with osteopenia and fractures at birth 2007 ·American Journal of Medical Genetics Part A ·Doris Taha,(unknown),Andrew R. Cullinane,Paul Gissen	16
20	The Meckel–Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation 2006 ·Human Molecular Genetics ·Helen R. Dawe,(unknown),Andrew R. Cullinane,Dianne Gerrelli,P. Cox,José L. Badano,(unknown),(unknown),Nicholas Katsanis,Tania Attié‐Bitach,Simon C. Afford,Andrew J. Copp,Déirdre Kelly,Keith Gull,Colin A. Johnson	202

About Andrew R. Cullinane

Andrew R. Cullinane is a scholar working on Hematology, Cell Biology and Immunology, having authored 20 papers that have together received 824 indexed citations. Recurring topics across this work include melanin and skin pigmentation (6 papers), Autoimmune and Inflammatory Disorders Research (5 papers) and Immune Cell Function and Interaction (4 papers). The work is most often cited by research in Genetics (401 citations), Cell Biology (205 citations) and Hematology (97 citations). Andrew R. Cullinane has collaborated with scholars based in United States, United Kingdom and France. Frequent co-authors include Marjan Huizing, Alejandro A. Schäffer, William A. Gahl, Konrad Krzewski, Thierry Vilboux, Meral Gunay‐Aygun, Helen R. Dawe, Déirdre Kelly, Andrew J. Copp and Simon C. Afford. Their work appears in journals such as Journal of Allergy and Clinical Immunology, Human Molecular Genetics and Journal of Investigative Dermatology.

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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