Tatiana B. Prokaeva, MD, PhD
Assistant Professor
Boston University Chobanian & Avedisian School of Medicine
Pathology & Laboratory Medicine

MD, Medical Semashko Institute
PhD, Russian Academy of Medical Sciences



Expertise in genetics of primary and familial types of amyloidosis.

Member
Boston University
Amyloidosis Center




SCAN-MP (Screening for Cardiac Amyloidosis with Nuclear Imaging in Minority Populations)
05/01/2019 - 02/29/2024 (Subcontract PI)
Boston Medical Center Corporation NIH NHLBI
5R01HL139671-04

Preclinical evaluation of amyloid binding on tissues and opsonization using CAEL-101
10/02/2022 - 10/01/2023 (PI)
Alexion Pharmaceuticals, Inc.


ALA Study - Janssen Pharmaceuticals
06/09/2020 - 06/09/2023 (PI)
Janssen Research & Development, LLC




Title


Yr Title Project-Sub Proj Pubs

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.

iCite Analysis       Copy PMIDs To Clipboard

  1. Morgan GJ, Nau AN, Wong S, Spencer BH, Shen Y, Hua A, Bullard MJ, Sanchorawala V, Prokaeva T. An updated AL-base reveals ranked enrichment of immunoglobulin light chain variable genes in AL amyloidosis. Amyloid. 2024 Dec 06; 1-10.View Related Profiles. PMID: 39641756
     
  2. Morgan GJ, Yung Z, Spencer BH, Sanchorawala V, Prokaeva T. Predicting Structural Consequences of Antibody Light Chain N-Glycosylation in AL Amyloidosis. Pharmaceuticals (Basel). 2024 Nov 16; 17(11).View Related Profiles. PMID: 39598451; PMCID: PMC11597191; DOI: 10.3390/ph17111542;
     
  3. Dodge MC, Prokaeva T, Mendelson L, Joshi T, Sanchorawala V, Kataria Y. High-Sensitivity and Conventional Cardiac Troponin-I Assays in AL Amyloidosis. J Appl Lab Med. 2024 Nov 04.View Related Profiles. PMID: 39495058
     
  4. Klimtchuk ES, Prokaeva T, Spencer BH, Wong S, Ghosh S, Urdaneta A, Morgan G, Wales TE, Gursky O. Conformational Differences in the Light Chain Constant Domain of Immunoglobulin G and Free Light Chain May Influence Proteolysis in AL Amyloidosis. J Mol Biol. 2024 Dec 01; 436(23):168837.View Related Profiles. PMID: 39490919
     
  5. Morgan G, Nau AN, Wong S, Spencer BH, Shen Y, Hua A, Bullard MJ, Sanchorawala V, Prokaeva T. An updated AL-Base reveals ranked enrichment of immunoglobulin light chain variable genes in AL amyloidosis. bioRxiv. 2024 Sep 15.View Related Profiles. PMID: 39314448; PMCID: PMC11419035; DOI: 10.1101/2024.09.11.612490;
     
  6. Urina-Jassir M, Teruya S, Blaner WS, Brun PJ, Prokaeva T, Tsai FJ, Kelly JW, Maurer MS, Ruberg FL. Differential Association of Transthyretin Stability with Variant and Wild-Type Transthyretin Amyloid Cardiomyopathy: The SCAN-MP Study. JACC Heart Fail. 2024 Dec; 12(12):2113-2115.View Related Profiles. PMID: 39115519
     
  7. Thel MC, Cochran JD, Teruya S, Hayashi O, Xie CR, Srinivasan AR, Chavkin NW, Arai Y, Sano S, Mirabal Santos A, De Los Santos J, Fine D, Sabogal N, Ullah I, Helmke S, Rodriguez C, Prokaeva T, Foster RH, Spencer BH, Izumiya Y, Maurer MS, Walsh K, Ruberg FL. Mosaic Loss of the Y Chromosome Is Enriched in Patients With Wild-Type Transthyretin Cardiac Amyloidosis and Associated With Increased Mortality. Circ Heart Fail. 2024 Aug; 17(8):e011681.View Related Profiles. PMID: 38853760; PMCID: PMC11335443; DOI: 10.1161/CIRCHEARTFAILURE.124.011681;
     
  8. Edwards CV, Ferri GM, Villegas-Galaviz J, Ghosh S, Bawa PS, Wang F, Klimtchuk E, Ajayi TB, Morgan GJ, Prokaeva T, Staron A, Ruberg FL, Sanchorawala V, Giadone RM, Murphy GJ. Abnormal global longitudinal strain and reduced serum inflammatory markers in cardiac AL amyloidosis patients without significant amyloid fibril deposition. bioRxiv. 2024 Mar 16.View Related Profiles. PMID: 38558967; PMCID: PMC10980073; DOI: 10.1101/2024.03.14.584987;
     
  9. Lau KHV, Prokaeva T, Zheng L, Doros G, Kaku MC, Spencer B, Berk J, Sanchorawala V. Neurofilament light chain kinetics as a biomarker for polyneuropathy in V122I hereditary transthyretin amyloidosis. Amyloid. 2024 Jun; 31(2):150-152.View Related Profiles. PMID: 38073425
     
  10. Mendelson L, Prokaeva T, Lau KHV, Sanchorawala V, McCausland K, Spencer B, Dasari S, McPhail ED, Kaku MC. Hereditary gelsolin amyloidosis: a rare cause of cranial, peripheral and autonomic neuropathies linked to D187N and Y447H substitutions. Amyloid. 2023 Dec; 30(4):357-363.View Related Profiles. PMID: 37140928
     
Showing 10 of 37 results. Show More

This graph shows the total number of publications by year, by first, middle/unknown, or last author.

Bar chart showing 37 publications over 18 distinct years, with a maximum of 8 publications in 2024

YearPublications
19901
19911
20001
20022
20032
20061
20073
20081
20092
20111
20122
20141
20162
20172
20182
20222
20233
20248

In addition to these self-described keywords below, a list of MeSH based concepts is available here.

familial amyloidosis
primary amyloidosis
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