Ashok Balasubramanyam

ORCID: 0000-0003-2093-5201

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 70 papers. Top paper: “SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia”.

SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia

Brain(2023)10.1093/brain/awac460

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0.992DataRank · unranked

35 citations

Hagar Mor Shaked, Kenneth Gable, Sita D. Gupta, Xueyang Pan, Niranjanakumari Somashekarappa +93 more

De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.02.016

N/A

0.639DataRank · unranked

70 citations

Chloe Reuter, Maura Ruzhnikov, Anita E. Beck, Emily Farrow, Lisa Emrick +91 more

Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment

npj Genomic Medicine(2023)10.1038/s41525-022-00343-8

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0.605DataRank · unranked

18 citations

Vikas Bhambhani, Nour Gazzaz, Mariska Davids, Paalini Sathiyaseelan, Ellen F. Macnamara +95 more

The cross-sectional association of cognition with diabetic peripheral and autonomic neuropathy—The GRADE study

Journal of Diabetes and its Complications(2021)10.1016/j.jdiacomp.2021.108047

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0.587DataRank · unranked

12 citations

Alokananda Ghosh, Rodica Pop‐Busui, Andrew Ahmann, Ashok Balasubramanyam, Mary Ann Banerji +7 more

Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

Genetics in Medicine(2020)10.1038/s41436-020-00984-z

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0.564DataRank · unranked

42 citations

Cecilia Esteves, Anna Bican, Rebecca C. Spillmann, Heidi Cope, Allyn McConkie‐Rosell +89 more

Mentored implementation to initiate a diabetes program in an underserved community: a pilot study

BMJ Open Diabetes Research & Care(2021)10.1136/bmjdrc-2021-002320

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0.457DataRank · unranked

20 citations

Aanand D. Naik, Amber B. Amspoker, Craig A. Johnston, Joshua D Landrum, Ashok Balasubramanyam +4 more

Association of Glycemia, Lipids, and Blood Pressure With Cognitive Performance in People With Type 2 Diabetes in the Glycemia Reduction Approaches in Diabetes: A Comparative Effectiveness Study (GRADE)

Diabetes Care(2021)10.2337/dc20-2858

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0.426DataRank · unranked

9 citations

Naji Younes, Jennifer J. Manly, Joshua I. Barzilay, Willy Marcos Valencia, Mary Larkin +94 more

De novo variants in DENND5B cause a neurodevelopmental disorder

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.02.001

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0.345DataRank · unranked

9 citations

Valeria Tomati, Matteo P. Ferla, Mariateresa Lena, Julie S. Cohen, Ali Fatemi +94 more

Erythritol, Erythronate, and Cardiovascular Outcomes in Older Adults in the ARIC Study

JACC Advances(2025)10.1016/j.jacadv.2025.101605

N/A

0.321DataRank · unranked

7 citations

Bing Yu, Ron C. Hoogeveen, Caroline Sun, Chao Cheng, Sean M. Hartig +8 more

Association of Type 2 Diabetes Subgroups With Cognitive Status Without Modification From Lifestyle Intervention

The Journal of Clinical Endocrinology & Metabolism(2022)10.1210/clinem/dgac706

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0.295DataRank · unranked

5 citations

James Lovato, Ashok Balasubramanyam, Mace Coday, Karen Johnson, Medha Munshi +4 more

Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2322582121

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0.292DataRank · unranked

6 citations

Oguz Kanca, Rishi V. Shridharan, Paul C. Marcogliese, Benjamin Steger, Marie Morimoto +92 more

Continuing a search for a diagnosis: the impact of adolescence and family dynamics

Orphanet Journal of Rare Diseases(2023)10.1186/s13023-022-02598-x

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0.292DataRank · unranked

6 citations

Beverly M. Yashar, Undiagnosed Disease Network, Maria T. Acosta, Margaret P Adam, David R. Adams +95 more

Does Emotional Distress Predict Worse Glycemic Control Over Time? Results From the Glycemia Reduction Approaches in Diabetes: A Comparative Effectiveness Study (GRADE)

Diabetes Care(2024)10.2337/dc23-0642

N/A

0.269DataRank · unranked

5 citations

Ionut Bebu, Heidi Krause‐Steinrauf, Claire J. Hoogendoorn, Gladys Crespo-Ramos, Caroline Presley +95 more

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

Nature Communications(2025)10.1038/s41467-025-61712-2

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0.269DataRank · unranked

5 citations

Mikhail A. Moldovan, Rebecca Reimers, Daniel Traviglia, Xinyun Li, Danielle Barnum +95 more

Association of Lifestyle Intervention With Risk for Cardiovascular Events Differs by Level of Glycated Hemoglobin

The Journal of Clinical Endocrinology & Metabolism(2023)10.1210/clinem/dgad674

N/A

0.208DataRank · unranked

3 citations

Scott J. Pilla, Ashok Balasubramanyam, Hsin‐Chieh Yeh, Karen Johnson, Joseph Rigdon +3 more

GAD65Abs Are Not Associated With Beta-Cell Dysfunction in Patients With T2D in the GRADE Study

Journal of the Endocrine Society(2024)10.1210/jendso/bvad179

N/A

0.165DataRank · unranked

2 citations

Ali Shojaie, Barbara Brooks‐Worrell, Sepideh Dibay, Kristina M. Utzschneider, Steven E. Kahn +12 more

Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome

Brain(2022)10.1093/brain/awac223

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0DataRank · unranked

16 citations

Aloran Mazumder, Daisuke Ogasawara, Rami Abou Jamra, Geneviève Bernard, Enrico Bertini +94 more

Optimal cardiometabolic health and risk of heart failure in type 2 diabetes: an analysis from the Look AHEAD trial

European Journal of Heart Failure(2022)10.1002/ejhf.2723

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0DataRank · unranked

14 citations

Muhammad Shahzeb Khan, Matthew W. Segar, Judy Bahnson, Katelyn R Garcia, Jeanne M. Clark +9 more

A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder

Genetics in Medicine(2022)10.1016/j.gim.2022.03.014

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0DataRank · unranked

16 citations

Kristin Grimsrud, Louise Lanoue, Alena Egense, Brandon Willis, Johanna Hörberg +95 more

Data Mining Framework for Discovering and Clustering Phenotypes of Atypical Diabetes

The Journal of Clinical Endocrinology & Metabolism(2022)10.1210/clinem/dgac632

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0DataRank · unranked

10 citations

Cassandra Remedios, Christiane S. Hampe, Ashok Balasubramanyam, Susan P. Fisher‐Hoch, Ye Ji Choi +5 more

Remission in Ketosis-Prone Diabetes

Endocrinology and Metabolism Clinics of North America(2022)10.1016/j.ecl.2022.06.005

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0DataRank · unranked

7 citations

Ashok Balasubramanyam, Nupur Kikani

Characteristics of Type 2 Diabetes in Female and Male Youth

Clinical Diabetes(2022)10.2337/cd22-0057

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0DataRank · unranked

6 citations

Marcela Astudillo, Mustafa Tosur, Ahmad Rafaey, Siripoom McKay, Fida Bacha +3 more

Mechanistic Investigation of GHS-R Mediated Glucose-Stimulated Insulin Secretion in Pancreatic Islets

Biomolecules(2022)10.3390/biom12030407

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0DataRank · unranked

7 citations

Jong Han Lee, Chia‐Shan Wu, Hongying Wang, Ligen Lin, Taraka Donti +7 more

A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

Genetics in Medicine(2022)10.1016/j.gim.2022.12.001

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0DataRank · unranked

1 citations

Queenie K.‐G. Tan, Chloe Reuter, Kelly Schoch, Jennefer N. Kohler, Devon Bonner +94 more

Bi-allelic variants in INTS11 are associated with a complex neurological disorder

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.012

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0DataRank · unranked

38 citations

Erica L. Macke, Marcello Niceta, Monika Weisz Hubshman, Oguz Kanca, Laura Schultz‐Rogers +95 more

Adipose Tissue Dysfunction and Energy Balance Paradigms in People Living With HIV

Endocrine Reviews(2023)10.1210/endrev/bnad028

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0DataRank · unranked

15 citations

Neeti Agarwal, Aaron R. Cox, Sean M. Hartig, Jordan E. Lake, Ashok Balasubramanyam +1 more

Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

Genetics in Medicine(2023)10.1016/j.gim.2023.100897

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0DataRank · unranked

10 citations

Kelly Schoch, Rebecca Ganetzky, Peter G. Kranz, Neal Sondheimer, M. Louise Markert +92 more

De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.012

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0DataRank · unranked

8 citations

Rossella Venditti, Evangelos A. Theodorou, Lauren C. Briere, Marion Rosello, Alfonsina Tirozzi +94 more

Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care

The Journal of Pediatrics(2023)10.1016/j.jpeds.2023.113537

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0DataRank · unranked

7 citations

Jennifer L. Young, Charis Tang, Kevin Mintz, Sawyer Lucas-Griffin, AudreyStephannie Maghiro +95 more

Type 1 Diabetes Genetic Risk Score Differentiates Subgroups of Ketosis-Prone Diabetes

Diabetes Care(2023)10.2337/dc23-0622

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0DataRank · unranked

6 citations

Surya N. Mulukutla, Christiane S. Hampe, Ruchi Gaba, Nalini Ram, Michael N. Weedon +3 more

De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

Genetics in Medicine(2023)10.1016/j.gim.2023.100833

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0DataRank · unranked

6 citations

Jung-Wan Mok, Oguz Kanca, Sharayu Jangam, Cynthia J. Tifft, Ellen F. Macnamara +95 more

Macrocephaly and developmental delay caused by missense variants in RAB5C

Human Molecular Genetics(2023)10.1093/hmg/ddad130

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0DataRank · unranked

4 citations

Weimin Yuan, Federico Tessadori, Wilmer R. Rodriguez-Polanco, Jeremy J. Grubbs, Bo Zhang +94 more

Energy balance and body composition after switch between integrase strand transfer inhibitors and doravirine among people with HIV

Journal of Antimicrobial Chemotherapy(2023)10.1093/jac/dkad363

N/A

0DataRank · unranked

3 citations

Ruda Mohaweche, Mary Morrow, Samantha MaWhinney, Vincent Khuu, Mallory Boyd +4 more

Large-scale mutational analysis identifies UNC93B1 variants that drive TLR-mediated autoimmunity in mice and humans

The Journal of Experimental Medicine(2024)10.1084/jem.20232005

N/A

0DataRank · unranked

37 citations

Julian A. Yano, John Huizar, Leianna C. Slayden, Madeleine A. Weiss, Elizabeth A Turcotte +93 more

A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2023.12.004

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0DataRank · unranked

14 citations

Sydney L. Michener, Hongling Pan, Hiuling Chan, Jessica M. Pfliger, Jill A. Rosenfeld +95 more

Atypical Diabetes: What Have We Learned and What Does the Future Hold?

Diabetes Care(2024)10.2337/dci23-0038

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0DataRank · unranked

14 citations

Ashok Balasubramanyam, Jennifer E. Posey, Stephen Stone

Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

Genetics in Medicine(2024)10.1016/j.gim.2024.101166

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0DataRank · unranked

11 citations

Nicole Legro, Dustin Baldridge, Jimann Shin, Angela Bowman, Berrak Uğur +89 more

Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

Genetics in Medicine(2024)10.1016/j.gim.2024.101115

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0DataRank · unranked

6 citations

Lauren C. Briere, Chloe Reuter, Perman Gochyyev, Maria T. Acosta, David R. Adams +94 more

Impact of Insulin Sensitivity and β-Cell Function Over Time on Glycemic Outcomes in the Glycemia Reduction Approaches in Diabetes: A Comparative Effectiveness Study (GRADE): Differential Treatment Effects of Dual Therapy

Diabetes Care(2024)10.2337/dc23-1059

N/A

0DataRank · unranked

7 citations

Naji Younes, Nicole M. Butera, Ashok Balasubramanyam, Richard M. Bergenstal, Joshua I. Barzilay +95 more

Long‐term sustained effects of the Look AHEAD lifestyle intervention on body composition among adults with type 2 diabetes

Obesity(2024)10.1002/oby.24025

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0DataRank · unranked

7 citations

Stanley Heshka, Andrea Anderson, Henry J. Pownall, Blandine Laferrère, Ashok Balasubramanyam +4 more

Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

Genetics in Medicine(2024)10.1016/j.gim.2024.101174

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0DataRank · unranked

4 citations

Kristhen N Atala, Yiming Zheng, Debdeep Dutta, Dorothy K. Grange, Wen‐Wen Lin +95 more

Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

Genetics in Medicine(2024)10.1016/j.gim.2024.101218

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0DataRank · unranked

4 citations

Kristy Jay, Alden Huang, Jijun Wan, Sharayu Jangam, Odelia Chorin +95 more

Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder

Pediatric Neurology(2024)10.1016/j.pediatrneurol.2024.07.010

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0DataRank · unranked

2 citations

Heena Patel, Siddharth Srivastava, Lindsay C. Swanson, Boris Keren, Sandra Whalen +95 more

LUSTR: a new customizable tool for calling genome-wide germline and somatic short tandem repeat variants

BMC Genomics(2024)10.1186/s12864-023-09935-9

N/A

0DataRank · unranked

0 citations

Camilo Toro, David R. Adams, Undiagnosed Diseases Network, Maria T. Acosta, Margaret P Adam +95 more

Glycemia Reduction in Type 2 Diabetes - Glycemic Outcomes

UNC Libraries(2024)10.17615/2s2m-qy50

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0DataRank · unranked

0 citations

Wexler D.J, Crandall J.P, Ashok Balasubramanyam, N Rasouli, Cohen R.M +10 more

The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

Genetics in Medicine(2024)10.1016/j.gim.2024.101203

N/A

0DataRank · unranked

0 citations

Laura Findley, Weihong Ni, Janet S. Sinsheimer, Francesca Cole, Cecilia Esteves +94 more

Identification of atypical pediatric diabetes mellitus cases using electronic medical records

BMJ Open Diabetes Research & Care(2024)10.1136/bmjdrc-2024-004471

N/A

0DataRank · unranked

0 citations

William E. Winter, Liana K. Billings, Raymond J. Kreienkamp, Ashok Balasubramanyam, María J. Redondo +2 more

An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser

Genome Medicine(2025)10.1186/s13073-025-01546-1

N/A

0DataRank · unranked

8 citations

Shruti Marwaha, Alistair Ward, Shilpa N. Kobren, Jennefer N. Carter, Undiagnosed Diseases Network +94 more

ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy

Genetics in Medicine(2025)10.1016/j.gim.2025.101506

N/A

0DataRank · unranked

3 citations

Chu-Ting Chang, A. Declève, Gloria Brunori, W.H. Ludlam, Alden Huang +93 more

De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies

Genetics in Medicine(2025)10.1016/j.gim.2025.101369

N/A

0DataRank · unranked

4 citations

Lindsay C. Burrage, Sharayu Jangam, Jill A. Rosenfeld, Sandra von Hardenberg, Anke K. Bergmann +92 more

Amino Acids and CART Distinguish A−β+ Ketosis-Prone Diabetes From Type 1 and Type 2 Diabetes During Hyperglycemic Crises

The Journal of Clinical Endocrinology & Metabolism(2025)10.1210/clinem/dgaf033

N/A

0DataRank · unranked

1 citations

Jean W. Hsu, Kelly Rogers Keene, W. Frank Peacock, Xiaofang Huang, Danielle Guffey +6 more

Enriched phenotypes in rare variant carriers suggest pathogenic mechanisms in rare disease patients

BioData Mining(2025)10.1186/s13040-024-00418-5

N/A

0DataRank · unranked

1 citations

Undiagnosed Diseases Network, Maria T. Acosta, David R. Adams, Ben Afzali, Ali Al-Beshri +95 more

Liver-specific Expression of HIV-1 Viral Protein R Causes Hepatic Steatosis and Glucose Intolerance in Male Mice

Journal of the Endocrine Society(2025)10.1210/jendso/bvaf132

N/A

0DataRank · unranked

0 citations

Pradip Saha, Claudia E. Ramirez, Sean M. Hartig, Mark A. Herman, Ashok Balasubramanyam +2 more

The clinical consequences of heterogeneity within and between different diabetes types

Diabetologia(2020)10.1007/s00125-020-05211-7

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0DataRank · unranked

187 citations

William Hagopian, Richard A. Oram, Andrea K. Steck, Kendra Vehik, Michael N. Weedon +3 more

Age-related variations in HbA1c improvements: insights from a telehealth-supported community-based intervention

Innovation in Aging(2025)10.1093/geroni/igaf121

N/A

0DataRank · unranked

0 citations

Xiaoying Yu, Amber B. Amspoker, Craig A. Johnston, Aanand D. Naik, Salim S. Virani +4 more

Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder

Brain(2020)10.1093/brain/awaa204

N/A

0DataRank · unranked

59 citations

Fanny Kortüm, Georg Christoph Korenke, Malik Alawi, René Santer, Mathias Woidy +95 more

An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Genetics in Medicine(2020)10.1038/s41436-020-01027-3

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0DataRank · unranked

49 citations

Kirsty McWalter, Heleen te Brinke, Lodewijk IJlst, Petra M. Mooijer, Jos P.N. Ruiter +95 more

The Effect of Ethnicity in the Rate of Beta-Cell Functional Loss in the First 3 Years After Type 1 Diabetes Diagnosis

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgaa348

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0DataRank · unranked

7 citations

Mario A. Cleves, Jay M. Sosenko, Ingrid Libman, David A. Baidal, Ashok Balasubramanyam +80 more

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Genetics in Medicine(2021)10.1038/s41436-021-01232-8

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0DataRank · unranked

49 citations

Rebecca C. Spillmann, Harley T. Kurata, Shawn M. Lamothe, Jasmine Maghera, Rami Abou Jamra +92 more

Type 2 Diabetes Subgroups, Risk for Complications, and Differential Effects Due to an Intensive Lifestyle Intervention

Diabetes Care(2021)10.2337/dc20-2372

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0DataRank · unranked

46 citations

Haiying Chen, Ashok Balasubramanyam, Alain G. Bertoni, Mark A. Espeland, Steven E. Kahn +4 more

Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

Genetics in Medicine(2021)10.1038/s41436-020-01084-8

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0DataRank · unranked

34 citations

Dustin Baldridge, Matt Velinder, Joel B. Krier, Kimberly LeBlanc, Cecilia Esteves +90 more

Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

Genetics in Medicine(2021)10.1038/s41436-021-01152-7

N/A

0DataRank · unranked

30 citations

Georgi Stoyanov, Florian Erger, Constantine A. Stratakis, Nikolaos Settas, Edra London +95 more

Toward an Improved Classification of Type 2 Diabetes: Lessons From Research into the Heterogeneity of a Complex Disease

The Journal of Clinical Endocrinology & Metabolism(2021)10.1210/clinem/dgab545

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26 citations

Ashok Balasubramanyam, María J. Redondo

Exome sequencing in children with clinically suspected maturity‐onset diabetes of the young

Pediatric Diabetes(2021)10.1111/pedi.13257

N/A

0DataRank · unranked

18 citations

Claudia Soler‐Alfonso, Katie Chan, Michael M. Khayat, Shalini N. Jhangiani, Qingchang Meng +9 more

The Moderating Effects of Genetic Variations on Changes in Physical Activity Level and Cardiorespiratory Fitness in Response to a Life-Style Intervention: A Randomized Controlled Trial

Psychosomatic Medicine(2021)10.1097/psy.0000000000000930

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2 citations

John E. McGeary, Shira Dunsiger, Laura D. Baker, Ashok Balasubramanyam, William C. Knowler +2 more

Type 2 Diabetes Subgroups, Risk for Complications, and Differential Effects Due to an Intensive Lifestyle Intervention

Figshare(2021)10.2337/figshare.13681747.v1

N/A

0DataRank · unranked

0 citations

Haiying Chen, Ashok Balasubramanyam, Alain G. Bertoni, Mark A. Espeland, S. M. Kahn +4 more

Type 2 Diabetes Subgroups, Risk for Complications, and Differential Effects Due to an Intensive Lifestyle Intervention

(2021)10.2337/figshare.13681747

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0DataRank · unranked

0 citations

Haiying Chen, Ashok Balasubramanyam, Alain G. Bertoni, Mark A. Espeland, S. M. Kahn +4 more

Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome

Annals of the Rheumatic Diseases(2022)10.1136/annrheumdis-2022-222629

N/A

0DataRank · unranked

70 citations

Shilpa Kodati, Laryssa A. Huryn, Hongying Wang, Blake M. Warner, Priyam Jani +95 more

Long-Term Effectiveness of the TIME Intervention to Improve Diabetes Outcomes in Low-Income Settings: a 2-Year Follow-Up

Journal of General Internal Medicine(2022)10.1007/s11606-021-07363-7

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20 citations

Evan Johnson, Aanand D. Naik, Amber B. Amspoker, Ashok Balasubramanyam, Salim S. Virani +4 more

The microRNA processorDROSHAis a candidate gene for a severe progressive neurological disorder

Human Molecular Genetics(2022)10.1093/hmg/ddac085

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17 citations

Mümine Şentürk, Kelly Schoch, Amanda L. Minogue, Diego Lopergolo, Chiara Fallerini +95 more